Overview of the Microcirculation

doi:10.1016/B978-0-12-374530-9.00022-X

Microcirculation (Second Edition)

Microcirculation

2008, Pages xi-xxiv

https://doi.org/10.1016/B978-0-12-374530-9.00022-X

References

[1]
Wiggers C.J.
Physiology in Health and Disease
Lea and Febiger, Philadelphia (1944)
p. 545
Google Scholar
[2]
Gauer O.H.
Harvey: William Harvey, “Founders of Experimental Physiology”
J.F. Lehmanns Verlag, Munchen (1971)
p. 111
Google Scholar
[3]
Landis E.M.
The capillary circulation
A.P. Fishman, D.W. Richards (Eds.), Circulation of the Blood, Men and Ideas, American Physiological Society, Bethesda, MD (1982)
Chapter VI
Google Scholar
[4]
Hoole S., Van Leeuwenhoek A.
Select Works Containing His Microscopical Discoveries in Many of the Works of Nature, Vol. 1, G. & W. Nicol, London (1798)
Translated by Samuel Hoole
[5]
Foster M.
A Textbook of Physiology
(5th Edition), Macmillan & Co, London and New York (1893)
Part I
Google Scholar
[6]
Pries A.R., Neuhaus D., Gaehtgens P.
Blood viscosity in tube flow: dependence on diameter and hematocrit
Am J Physiol, 263 (1992), pp. H1770-H1778
Google Scholar
[7]
Krogh A.
Anatomy and Physiology of Capillaries
Yale University Press, New Haven, Connecticut (1929)
Google Scholar
[8]
Popel A.S., Torres Filho I.P., Johnson P.C., Bouskela E.
A new scheme for hierarchical classification of anastomosing vessels
Int J Microcirc Clin Exp, 7 (1988), pp. 131-138
Google Scholar
[9]
Wiedeman M.P.
Lengths and diameters of peripheral arterial vessels in the living animal
Circ Res, 10 (1962), pp. 686-690
Google Scholar
[10]
Gaehtgens P., Ley K., Pries A.R.
Topological approach to the analysis of microvessel structure and hematocrit distribution
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 52-60
Google Scholar
[11]
Strahler A.N.
Quantitative analysis of watershed morphology
Trans Am Geophys Union, 38 (1957), pp. 913-920
Google Scholar
[12]
TorresFilho I.P., Popel A.S., Johnson P.C., Cyrino F.Z.G.A., Bouskela E.
Shape and orientation of arterial loops in cat sartorius muscle
Int J Microcirc: Clin Exp, 9 (1990), pp. 297-302
Google Scholar
[13]
Joyner W.L., Davis M.J., Gilmore J.P.
Intravascular pressure distribution and dimensional analysis of microvessels in hamsters with renovascular hypertension
Microvasc Res, 22 (1981), pp. 190-198
Google Scholar
[14]
Kuo L., Davis M.J., Chilian W.M.
Myogenic activity in isolated subepicardial and subendocardial coronary arterioles
Am J Physiol, 255 (1988), pp. H1558-H1562
Google Scholar
[15]
Sakai H., Hara H., Tsai A.G., Tsuchida E., Intaglietta M.
Constriction of resistance arteries determines l-NAME-induced hypertension in a conscious hamster model
Microvasc Res, 60 (2000), pp. 21-27
Google Scholar
[16]
Rhodin J.A.G.
The ultrastructure of mammalian arterioles and precapillary sphincters
J Ultrastruct Res, 18 (1967), pp. 181-223
Google Scholar
[17]
Schmid-Schoenbein G.W., Skalak T.C., Engelson E.T., Zweifach B.W.
Microvascular network anatomy in rat skeletal muscle
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 38-51
Google Scholar
[18]
Sullivan S.M., Johnson P.C.
Effect of oxygen on arteriolar dimensions and blood flow in cat sartorius muscle
Am J Physiol, 241 (1981), pp. H547-H556
Google Scholar
[19]
Smaje L., Zweifach B.W., Intaglietta M.
Micropressures and capillary filtration coefficients in single vessels of the cremaster muscle of the rat
Microvasc Res, 2 (1970), pp. 96-110
Google Scholar
[20]
Chambers R., Zweifach B.W.
Topography and function of the mesenteric capillary circulation
Am J Anat, 75 (1944), pp. 173-206
Google Scholar
[21]
Fuxe K., Sedvall G.
The distribution of adrenergic nerve fibres to the blood vessels in skeletal muscle
Acta Physiol Scand, 64 (1965), pp. 75-86
Google Scholar
[22]
Dodd L.R., Johnson P.C.
Diameter changes in arteriolar networks of contracting skeletal muscle
Am J Physiol, 260 (1991), pp. H662-H670
Google Scholar
[23]
Segal S.S.
Integration of blood flow control to skeletal muscle: key role of feed arteries
Acta Physiol Scand, 168 (2000), pp. 511-518
Google Scholar
[24]
Emerson G.G., Segal S.S.
Electrical activation of endothelium evokes vasodilation and hyperpolarization along hamster feed arteries
Am J Physiol, 280 (2001), pp. H160-H167
Google Scholar
[25]
Rhodin J.A.
Ultrastructure of mammalian venous capillaries, venules and small collecting veins
J Ultrastructure Res, 25 (1968), pp. 452-500
Google Scholar
[26]
Majno G.
Ultrastructure of the vascular membrane
W.F. Hamilton (Ed.), Handbook of Physiology, Circulation, Vol. III, American Physiological Society, Washington, DC (1965), pp. 2293-2375
Chapter 64, Section 2
Google Scholar
[27]
Reilly F.D., McCuskey R.S., Cilento E.V.
Hepatic microvascular regulatory mechanisms: I
Adrenergic mechanisms. Microvasc Res,, 21 (1981), pp. 103-116
Google Scholar
[28]
Eriksson E., Mryhage R.
Microvascular dimensions and blood flow in skeletal muscle
Acta Physiol Scand, 86 (1972), pp. 211-222
Google Scholar
[29]
Bassingthwaite J.B., Yipintsoi T., Harvey R.B.
Microvasculature of the dog left ventricular myocardium
Microvasc Res, 7 (1974), pp. 229-249
Google Scholar
[30]
Altman P. Blood and Other Body Fluids, eds Ditmer D and Washington DC. FASEB, 1961, p. 119.
Google Scholar
[31]
Ley K., Pries A.R., Gaehtgens P.
Topological structure of the rat mesenteric microvessel networks
Microvasc Res, 32 (1986), pp. 315-332
Google Scholar
[32]
Clark E.R., Clark E.L.
Observations on living arterio-venous anastomoses as seen in transparent chambers introduced into the rabbit's ear
Am J Anat, 54 (1934), pp. 229-286
Google Scholar
[33]
House S.D., Johnson P.C.
Diameter and blood flow of skeletal muscle venules during local flow regulation
Am J Physiol, 250 (1986), pp. H828-H837
Google Scholar
[34]
Koller A., Dawant B., Popel A.S., Johnson P.C.
Quantitative analysis of arteriolar network architecture in cat sartorius muscle
Am J Physiol, 253 (1987), pp. H154-H164
Google Scholar
[35]
Marshall J.M., Hebert M.T.
Differential effect of changes in sympathetic activity on consecutive sections of microcirculation of mesentery and skeletal muscle
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 123-133
Google Scholar
[36]
Bohlen H.G., Gore R.W.
Comparison of microvascular pressures and diameters in the innervated and denervated rat intestine
Microvasc Res, 14 (1977), pp. 251-264
Google Scholar
[37]
Pappenheimer J.R.
Contributions to microvascular research of Jean Leonard Marie Poiseulle
E.M. Renkin, C.C. Michel (Eds.), Handbook of Physiology, Section 2: The Cardiovascular System, Volume IV, American Physiological Society, Washington (1984)
Chapter 1, Microcirculation, Part 1
Google Scholar
[38]
Mall J.P.
Die Blut und Lymphwege im Dunndarm des Hundes
Abhandlungen der mathematischphysischen Classe der konigl Sachischen Gesellschaft der Wissenschaften, 14 (3) (1887)
Google Scholar
[39]
Schlier J.
Der energieverbrauch in der blutbahn
Pfluegers Archiv fuer die gesamte Physiologie des Menschen und der Tiere, 173 (1918), pp. 172-204
Google Scholar
[40]
Green HD. “Medical Physics”, ed. Glasser O. Chicago: Year Book Publ, 1944.
Google Scholar
[41]
Fronek K., Zweifach B.W.
Microvascular pressure distribution in skeletal muscle and the effect of vasodilatation
Am J Physiol, 228 (1975), pp. 791-796
Google Scholar
[42]
Schmid-Schoenbein G.W., Muakami H.
Blood flow in contracting arterioles
Int J Microcirc Clin Exp, 4 (1981, 1985), pp. 311-328
[43]
Johnson P.C.
Landis Award Lecture 1976. The myogenic response and the microcirculation
Microvasc Res, 13 (1977), pp. 1-18
Google Scholar
[44]
Smiesko V., Lang D.J., Johnson P.C.
Dilator response of rat mesenteric arcading arterioles to increased flow
Am J Physiol, 257 (1989), pp. H1958-H1965
Google Scholar
[45]
Christensen K.L., Mulvany M.J.
Location of resistance arteries
J Vasc Res, 38 (2001), pp. 1-12
Google Scholar
[46]
Clifford P.S., Hellsten Y.
Vasodilatory mechanisms in contracting skeletal muscle
J Appl Physiol, 97 (2004), pp. 393-403
Google Scholar
[47]
Hester R.L., Hammer L.W.
Venular-arteriolar communication in the regulation of blood flow
Am J Physiol, 282 (2002), pp. R1280-R1285
Google Scholar
[48]
Tigno X.T., Ley K., Pries A.R., Gaehtgens P.
Venulo-arteriolar communication and propagated response. A possible mechanism for local control of blood flow
Pflugers Arch, 414 (1989), pp. 450-456
Google Scholar
[49]
Zweifach B.W.
The structure and reaction of small blood vessels in amphibia
Am J Anat, 60 (1937), pp. 473-514
Google Scholar
[50]
Clark E.R., Clark E.L.
Caliber changes in minute blood vessels observed in the living mammal
Am J Anat, 73 (1943), pp. 215-250
Google Scholar
[51]
Gorcznski R.J., Klitzman B., Duling B.R.
Interrelations between contracting striated muscle and precapillary microvessels
Am J Physiol, 235 (1978), pp. H494-H504
Google Scholar
[52]
Zweifach B.W.
The microcirculatory module, myth or reality?
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 1-11
Google Scholar
[53]
Mayrovitz H.N.
Hemodynamic significance of microvascular arteriolar anastomosing
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 197-209
Google Scholar
[54]
Renkin E.M.
Control of circulation and blood-tissue exchange (Chapter 14)
E.M. Renkin, C.C. Michel (Eds.), Handbook of Physiology, Section 2: The Cardiovascular System Vol IV Microcirculation, Part 2, American Physiological Society, Bethesda (1984)
Google Scholar
[55]
Stromberg D.D., Fox J.R.
Pressures in the pial arterial microcirculation of the cat during changes in systemic arterial blood pressure
Circ Res, 31 (1972), pp. 229-239
Google Scholar
[56]
Schretzenmayr A.
Uber kreislaufregulatorische Vorgange an den grossen Arterien bei der Muskelarbeit
Pfluegers Arch, 232 (1933), pp. 743-748
Google Scholar
[57]
Hilton S.
A peripheral arterial conducting mechanism underlying dilation of the femoral artery and concerned in functional vasodilatation in skeletal muscle
J Physiol Lond, 149 (1959), pp. 93-111
Google Scholar
[58]
Khayutin V., Melkumyants A.M., Rogoza A.N., Veselova E.S., Balashov S.A., Nikolsky V.P.
Flow-induced control of the arterial lumen
Acta Physiol Hung, 68 (1986), pp. 241-251
Google Scholar
[59]
Rubanyi G.M., Romero C.J., Vanhoutte P.M.
Flow-induced release of endothelium-derived relaxing factor
Am J Physiol, 250 (1986), pp. H1145-H1149
Google Scholar
[60]
Pries A.R., Secomb T.W., Jacobs H., Sperandio M., Osterloh K., Gaehtgens P.
Microvascular flow resistance: role of endothelial surface layer
Am J Physiol, 273 (1997), pp. H2272-H2279
Google Scholar
[61]
Cabel M., Meiselman H.J., Popel A.S., Johnson P.C.
Contribution of red blood cell aggregation to venous vascular resistance in skeletal muscle
Am J Physiol, 272 (1997), pp. H1020-H1032
Google Scholar
[62]
Kuo L., Arko F., Chilian W.M., Davis M.J.
Coronary venular responses to flow and pressure
Circ Res, 72 (1993), pp. 607-615
Google Scholar
[63]
Bishop J.J., Nance P.R., Popel A.S.
Intaglietta M and Johnson PC
Diameter changes in skeletal muscle venules during arterial pressure reduction. Am J Physiol,, 279 (2000), pp. H47-H57
Google Scholar
[64]
Laughlin H.M., Joyner M.
Closer to the edge? Contractions, pressures, waterfalls and blood flow to contracting skeletal muscle
J Appl Physiol, 94 (2003), pp. 3-5
Google Scholar
[65]
Krogh A.
Supply of oxygen to the tissues and the regulation of the capil1ary circulation
J Physiol (Lond), 52 (1919), pp. 457-474
Google Scholar
[66]
Duling B.R., Berne R.M.
Longitudinal gradients in periarteriolar oxygen tension: Possible mechanism for the participation of oxygen in local regulation of blood flow
Circ Res, 27 (1970), pp. 669-678
Google Scholar
[67]
Tsai A.G., Friesnecker B., Mazzoni M.D., Kerger H., Buerk D.G., Johnson P.C., Intaglietta M.
Microvascular and tissue oxygen gradients in the rat mesentery
Proc Natl Acad Sci USA, 95 (1998), pp. 6590-6595
Google Scholar
[68]
Tsai A.G., Johnson P.C., Intaglietta M.
Oxygen gradients in the microcirculation
Physiol Rev, 83 (2003), pp. 933-963
Google Scholar
[69]
Wagner P.D.
Diffusional resistance to O2 transport in muscle
Acta Physiol Scand, 168 (2000), pp. 609-614
Google Scholar
[70]
Starling E.
On the absorption of fluids from the connective tissue spaces
J Physiol (Lond), 19 (1896), pp. 312-326
Google Scholar
[71]
Landis E.M.
Mirco-injection studies of capillary permeability: II the relation between capillary pressure and the rate at which fluid passes through the walls of single capillaries
Am J Physiol, 82 (1927), pp. 217-238
Google Scholar
[72]
Pappenheimer J.R., Soto Rivera A.
Effective osmotic pressure of the plasma proteins and other quantities associated with the capillary circulation in the hindlimbs of cats and dogs
Am J Physiol, 152 (1948), pp. 471-491
Google Scholar
[73]
Guyton A.C.
A concept of negative interstitial pressure based on pressures in implanted perforated capsules
Circ Res, 12 (1963), pp. 399-414
Google Scholar
[74]
Wiederhielm C.A., Weston B.V.
Microvascular, lymphatic and tissue pressures in the unanesthetized mammal
Am J Physiol, 225 (1973), pp. 992-996
Google Scholar
[75]
Johnson P.C.
Effect of venous pressure on mean capillary pressure and vascular resistance in the intestine
Circ Res, 16 (1965), pp. 294-300
Google Scholar
[76]
Mortillaro N.A., Taylor A.E.
Interaction of capillary and tissue forces in the cat small intestine
Circ Res, 39 (1976), pp. 348-358
Google Scholar
[77]
Chambers R., Zweifach B.W.
Intercellular cement and capillary permeability
Physiol Rev, 27 (1947), pp. 436-463
Google Scholar
[78]
Pappenheimer J.R., Renkin E.M., Borrero J.M.
Filtration, diffusion and molecular sieving through peripheral capillary membranes. A contribution to the pore theory of capillaray permeability
Am J Physiol, 167 (1951), pp. 13-46
Google Scholar
[79]
Michel C.C., Curry F.E.
Microvascular permeability
Physiol Rev, 79 (1999), pp. 703-761
Google Scholar
[80]
Levick J.R.
Capillary filtration-absorption balance reconsidered in light of dynamic extravascular factors
Exp Physiol, 76 (1991), pp. 825-857
Google Scholar
[81]
Wolf M.D., Watson P.D.
Measurement of osmotic reflection coefficient for small molecules in cat hindlimbs
Am J Physiol, 256 (1989), pp. H282-H290
Google Scholar
[82]
Grotte G.
Passage of dextran molecules across the blood-lymph barrier
Acta Chir Scand, 211 (Suppl.) (1956), pp. 1-84
Google Scholar
[83]
Palade G.E.
Transport in quanta across the endothelium of blood capillaries
Anat Rec, 136 (1960), p. 254
(abstract)
Google Scholar
[84]
Majno G., Palade G.E., Schoefl G.
Studies on inflammation II. The site of action of histamine and serotonin along the vascular tree: a topographic study
J Biophys Biochem Cytol, 11 (1961), pp. 607-626
Google Scholar
[85]
Yuan Y., Chilian W.M., Granger H.J., Zaweija D.C.
Flow modulates coronary venular permeability by a nitric oxide-related mechanism
Am J Physiol, 263 (1992), pp. H641-H646
Google Scholar
[86]
Dutrochet H.
Recherches anatomiques et physiologiques sur la structure intime des animaux et des végetaux, et sur leur motilité
Bailliere et fils, Paris (1824)
Google Scholar
[87]
Ohashi K.L., Tung K-L., Wilson J., Zweifach B.W., Schmid-Schoenbein G.
Transvascular and Interstitial migration of neutrophils in rat mesentery
Microcirculation, 3 (1996), pp. 199-210
Google Scholar
[88]
Tsai M.A., Frank R.S., Waugh R.E.
Passive mechanical behavior of human neutrophils: power-law fluid
Biophys J, 65 (1994), pp. 2078-2088
Google Scholar
[89]
Burns A.R., Walker D.C., Brown E.S., Thurmon L.T., Bowden R.A., Keese C.R., Simon S.I., Entman M.L., Smith C.W.
Neutrophil transendothelial migration is independent of tight junctions and occurs preferentially at tricellular corners
J Immunol, 159 (1997), pp. 2893-2903
Google Scholar
[90]
Damon D.H., Duling B.R.
Distribution of capillary blood flowin the microcirculation of the hamster. An in vivo study using epifluorescent microscopy
Microvasc Res, 27 (1984), pp. 81-95
Google Scholar
[91]
Unthank J.L., Lash J.M., Nixon J., Snider R.A., Bohlen H.G.
Evaluation of carbocyanine-labeled erythrocytes for microvascular measurements
Microvasc Res, 45 (1993), pp. 193-210
Google Scholar
[92]
Tangelder G.J., Slaaf D.W., Muijtjens A.M.M., Arts T.
oude Egbrink MGA and Reneman RS. Velocity profiles of blood platelets and red blood cells flowing in arterioles of the rabbit mesentery
Circ Res, 59 (1986), pp. 505-514
Google Scholar
[93]
Paques M., Boval B., Richard S., Tadayoni R., Massin P., Mundler O., Gaudric A., Vicaut E.
Evaluation of fluorescein-labeled autologous leukocytes for examination of retinal circulation in humans
Curr Eye Res, 21 (2000), pp. 560-565
Google Scholar
[94]
Adamson R.H., Lenz J.F., Curry F.E.
Quantitative laser scanning confocal microscopy on single capillaries: permeability measurement
Microcirculation, 1 (1994), pp. 251-265
Google Scholar
[95]
Chaigneau E., Oheim M., Audinat E., Charpak S.
Two-photon imaging of capillary blood flow in olfactory bulb glomeruli
Proc Natl Acad Sci USA, 100 (2003), pp. 13081-13086
Google Scholar
[96]
Beacham W.S., Konishi A., Hunt C.C.
Observations of the microcirculatory bed in rat mesocecum using differential interference contrast microscopy in vivo and electron microscopy
Am J Anat, 146 (1976), pp. 385-425
Google Scholar
[97]
Trache A., Meininger G.A.
Atomic force-multi-optical imaging integrated microscope for monitoring molecular dynamics in live cells
J Biomed Opt, 10 (2005)
064023
Google Scholar
[98]
Messmer K., Sunder-Plassmann L., Jesch F., Gornandt L., Sinagowitz E., Kessler M.
Oxygen supply to the tissues during limited normovolemic hemodilution
Res Exp Med (Berl), 159 (1973), pp. 152-166
Google Scholar
[99]
Whalen W.J., Riley J., Nair P.
Microelectrode for measuring intracellular PO2
J Appl Physiol, 23 (1967), pp. 798-801
Google Scholar
[100]
Lund N., Sjoberg F., Guldbrand H., Walfridsson H., Edwall G.
A multipoint micro antimony pH electrode for tissue surface measurements
Int J Clin Monit Comput, 1 (1984), pp. 147-153
Google Scholar
[101]
Bohlen H.G.
Mechanism of increased vessel wall nitric oxide concentrations during intestinal absorption
Am J Physiol, 275 (1998), pp. H542-H550
Google Scholar
[102]
Buerk D.G., Riva C.E., Cranstoun
Nitric oxide has a vasodilatory role in cat optic nerve head during flicker stimuli
Microvasc Res, 52 (1996), pp. 13-26
Google Scholar
[103]
Pittman R.N.
Microvessel blood oxygen measurement techniques
C.H. Baker, W.L. Nastuk (Eds.), Microcirulatory Technology, Academic, Orlando Fl (1987), pp. 367-390
Google Scholar
[104]
Mayhan W.G.
Nitric oxide accounts for histamine-induced increases in macromolecular extravasation
Am J Physiol, 266 (1994), pp. H2369-H2373
Google Scholar
[105]
Wilson D.F.
Measuring oxygen using oxygen dependent quenching of phosphorescence: A status report
Adv Exp Med Bio, 333 (1993), pp. 225-232
Google Scholar
[106]
Zheng L., Golub A.S., Pittman R.N.
Determination of pO2 and its heterogeneity in single capillaries
Am J Physiol, 271 (1996), pp. H365-H372
Google Scholar
[107]
Torres Filho I.P., Intaglietta M.
Microvessel pO2 measurements by phosphorescence decay method
Am J Physiol, 265 (1993), pp. H1434-H1438
Google Scholar
[108]
Buerk D.G., Tsai A.G., Intaglietta M., Johnson P.C.
In vivo tissue pO₂ measurements in hamster skinfold by recessed pO₂ microelectrodes and phosphorescence quenching are in agreement
Microcirculation, 5 (1998), pp. 219-225
Google Scholar
[109]
Toth A., Tischler M.E., Pal M., Koller A., Johnson P.C.
A multipurpose instrument for quantitative intravital microscopy
J Appl Physiol, 73 (1992), pp. 296-306
Google Scholar
[110]
Loutzenhiser R.D.
In situ studies of renal arteriolar function using the in vitro-perfused hydronephrotic rat kidney
Int Rev Exp Pathol, 36 (1996), pp. 145-160
Google Scholar
[111]
Munro P.A.G.
Methods for measuring the velocity of moving particles under the microscope
R. Barer, V.E. Cosslett (Eds.), Advances in Optical and Electron Microscopy, vol. 1, Academic, New York (1966), pp. 1-40
Google Scholar
[112]
Bloch E.H.
Quantitative study of the hemodynamics in the living microvascular system
Am J Anat, 110 (1962), pp. 125-153
Google Scholar
[113]
Intaglietta M., Tompkins W.R.
On-line measurement of microvascular dimensions by television microscopy
J Appl Physiol, 32 (1983), pp. 546-551
Google Scholar
[114]
Wayland H., Johnson P.C.
Erythrocyte velocity measurement in microvessels by a two-slit photometric method
J Appl Physiol, 22 (1967), pp. 333-337
Google Scholar
[115]
Intaglietta M., Tompkins W.R.
System for the measurement of velocity of microscopic particles in liquids
IEEE Trans Biomed, 18 (1971), pp. 376-377
Google Scholar
[116]
Baker M., Wayland H.
On-line volume flow rate velocity profile measurement for blood in microvessels
Microvasc Res, 7 (1974), pp. 131-143
Google Scholar
[117]
Davis M.J.
Determination of volumetric flow in capillary tubes using an optical Doppler velocimeter
Microvasc Res, 34 (1987), pp. 223-230
Google Scholar
[118]
Bishop J.J., Nance P.R., Popel A.S., Intaglietta M., Johnson P.C.
Relationship between erythrocyte aggregate size and flow rate in skeletal muscle venules
Am J Physiol, 286 (2004), pp. H113-H120
Google Scholar
[119]
Sarelius I.H., Duling B.R.
Direct measurement of microvessel hematocrit, red cell flux, velocity and transit time
Am. J. Physiol, 243 (1982), pp. H1018-H1026
Google Scholar
[120]
Bishop J.J., Nance P.R., Popel A.S., Intaglietta M., Johnson P.C.
Effect of erythrocyte aggregation on velocity profiles in venules
Am. J. Physiol, 280 (2001), pp. H222-H236
Google Scholar
[121]
Smith M.L., Long D.S., Damiano E.R., Ley K.
Near wall PIV reveals a hydrodynamically relevant endothelial surface layer in venules in vivo
Biophys. J, 85 (2003), pp. 637-645
Google Scholar
[122]
Roy C.S., Brown J.G.
The blood pressure and its variations in the arterioles, capillaries and veins
J. Physiol (Lond), 2 (1880), pp. 323-359
Google Scholar
[123]
Landis E.M.
The capillary pressure in frog mesentery as determined by micro-injection methods
Am J Physiol, 75 (1926), pp. 548-570
Google Scholar
[124]
Wiederhielm C.A., Woodbury J.W., Kirk S., Rushmer R.F.
Pulsatile pressures in the microcirculation of the frog's mesentery
Am J Physiol, 207 (1964), pp. 173-176
Google Scholar
[125]
Intaglietta M., Tompkins W.R.
Micropressure measurement with 1 micron and smaller cannulae
Microvasc Res, 3 (1971), pp. 211-214
Google Scholar
[126]
Segal S.S., Beny J.L.
Intracellular recording and dye transfer in arterioles during blood flow control
Am J Physiol, 263 (1992), pp. H1-H7
Google Scholar
[127]
Beach J.M., McC\Gahren E.F., Xia J., Duling B.R.
Ratiometric measurement of endothelial depolarization in arterioles with a potential-sensitive dye
Am J Physiol, 270 (1996), pp. H2216-H2227
Google Scholar
[128]
Nicoll P.A., Webb R.L.
Vascular patterns and active vasomotion as determiners of flow through minute vessels
Angiology, 6 (1955), pp. 291-308
Google Scholar
[129]
Microcirculatory Research Methods. Microvascular Research 5: 229–435, 1973.
Google Scholar
[130]
Baez S.
An open cremaster muscle preparation for the study of blood vessels by in vivo microscopy
Microvasc Res, 5 (1973), pp. 384-394
Google Scholar
[131]
Hill M.A., Simpson B.E., Meininger G.A.
Altered cremaster muscle hemodynamics due to disruption of the deferential feed vessels
Microvasc Res, 39 (1990), pp. 349-363
Google Scholar
[132]
Gore R.W.
Mesenteric preparations for quantitative microcirculatory studies
Microvasc Res, 5 (1973), pp. 368-375
Google Scholar
[133]
Frasher W.G. Jr.
Attached floating cat mesentery preparation for vital microscopy
Microvasc Res, 5 (1973), pp. 376-383
Google Scholar
[134]
Gray S.D.
Rat spinotrapezius muscle preparation for microscopic observation of the terminal vascular bed
Microvasc Res, 5 (1973), pp. 395-400
Google Scholar
[135]
Klotz K.F., Pries A.R., Jepsen H., Gossrau R., Gaehtens P.
A new approach to videomicroscopy of rat spinotrapezius muscle
Int J Microcirc Clin Exp, 10 (1991), pp. 205-218
Google Scholar
[136]
Zweifach B.W., Intaglietta M.
Mechanics of fluid movement across single capillaries in the rabbit
Microvasc Res, 1 (1968), pp. 83-101
Google Scholar
[137]
Lindbom L., Arfors K.E.
Mechanisms and site of control for variation in the number of perfused capillaries in skeletal muscle
Int J Microcirc Clin Exp, 4 (1985), pp. 19-30
Google Scholar
[138]
Burton K.M.
Cat sartorius muscle: an istolated perfused skeletal muscle preparation for microvascular research
Microvasc Res, 5 (1973), pp. 401-409
Google Scholar
[139]
Stromberg D.D., Shapiro H.M.
Preparation of the cat cerebral cortical surface for microvascular pressure measurements
Microvasc Res, 5 (1973), pp. 410-416
Google Scholar
[140]
Duling B.R.
The preparation and use of the hamster cheek pouch for studies of the microcirculation
Microvasc Res, 5 (1973), pp. 423-429
Google Scholar
[141]
Sullivan S.M., Pttman R.N.
Hamster retractor muscle: a new preparation for intravital microscopy
Microvasc Res, 23 (1982), pp. 329-335
Google Scholar
[142]
Wiedeman M.P.
Preparation of the bat wing for in vivo microscopy
Microvasc Res, 5 (1973), pp. 417-422
Google Scholar
[143]
Papenfuss H.D., Gross J.F., Intaglietta M., Treese F.A.
A transparent access chamber for the rat dorsal skin fold
Microvasc Res, 18 (1979), pp. 311-318
Google Scholar
[144]
Endrich B., Asaishi K., Götz A., Messmer K.
Technical report – a new chamber technique for microvascular studies in unanesthetized hamsters
Res Exp Med (Berl), 177 (1980), pp. 125-134
Google Scholar
[145]
Menger M.D., Jäger S., Walter P., Hammersen F., Messmer K.
A novel technique for studies on the microvasculature of transplanted islets of Langerhans in vivo
Int J Microcirc Clin Exp, 9 (1990), pp. 103-117
Google Scholar
[146]
Wiedeman M.P.
Patterns of the arteriovenous pathways
W.F. Hamilton, P. Dow, D.C. Washington (Eds.), Handbook of Physiology, vol. 11, American Physiological Society (1963), pp. 891-933
section 2
Google Scholar
[147]
Carpentier P., Franco A.
L'angioscopie conjunctivale DELTACOM
Boulogne-billancourt, France (1985)
Google Scholar
[148]
Fagrell B., Fronek A., Intaglietta M.
A microscope-television system for studying flow velocity in human skin capillaries
Am J Physiol, 233 (1977), pp. H318-H321
Google Scholar
[149]
Seifert H., Jäger K., Bollinger A.
Laser-Doppler probes for the evaluation of arterial ischemia
Adv Exp Med Biol, 220 (1987), pp. 227-229
Google Scholar
[150]
Slaaf D.W., Tangelder G.J., Reneman R.S., Jager K., Bollinger A.
A versatile incident illuminator for intravital microcscopy
Int J Microcirc Clin Exp, 6 (1987), pp. 391-397
Google Scholar
[151]
Mathura K.R., Vollebregt K.C., Boer K., De Graaff J.C., Ubbink D.T., Ince C.
Comparison of OPS imaging and conventional capillary microscopy to study the human microcirculation
J Appl Physiol, 91 (2001), pp. 74-78
Google Scholar
[152]
Huch A., Franzeck U.K., Huch R., Bollinger A.
A transparent transcutaneous oxygen electrode for simultaneous studies of skin capillary morphology, flow dynamics and oxygenation
Int J Microcirc Clin Exp, 2 (1983), pp. 103-108
Google Scholar
[153]
Kubli S., Waeber B., Dalle-Ave A., Feihl F.
Reproducibility of laser Doppler imaging of skin blood flow as a tool to assess endothelial function
J Cardiovasc Pharmacol, 36 (2000), pp. 640-648
Google Scholar

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[1] [1]
Wiggers C.J.
Physiology in Health and Disease
Lea and Febiger, Philadelphia (1944)
p. 545
Google Scholar

[2] [2]
Gauer O.H.
Harvey: William Harvey, “Founders of Experimental Physiology”
J.F. Lehmanns Verlag, Munchen (1971)
p. 111
Google Scholar

[3] [3]
Landis E.M.
The capillary circulation
A.P. Fishman, D.W. Richards (Eds.), Circulation of the Blood, Men and Ideas, American Physiological Society, Bethesda, MD (1982)
Chapter VI
Google Scholar

[4] [4]
Hoole S., Van Leeuwenhoek A.
Select Works Containing His Microscopical Discoveries in Many of the Works of Nature, Vol. 1, G. & W. Nicol, London (1798)
Translated by Samuel Hoole

[5] [5]
Foster M.
A Textbook of Physiology
(5th Edition), Macmillan & Co, London and New York (1893)
Part I
Google Scholar

[6] [6]
Pries A.R., Neuhaus D., Gaehtgens P.
Blood viscosity in tube flow: dependence on diameter and hematocrit
Am J Physiol, 263 (1992), pp. H1770-H1778
Google Scholar

[7] [7]
Krogh A.
Anatomy and Physiology of Capillaries
Yale University Press, New Haven, Connecticut (1929)
Google Scholar

[8] [8]
Popel A.S., Torres Filho I.P., Johnson P.C., Bouskela E.
A new scheme for hierarchical classification of anastomosing vessels
Int J Microcirc Clin Exp, 7 (1988), pp. 131-138
Google Scholar

[9] [9]
Wiedeman M.P.
Lengths and diameters of peripheral arterial vessels in the living animal
Circ Res, 10 (1962), pp. 686-690
Google Scholar

[10] [10]
Gaehtgens P., Ley K., Pries A.R.
Topological approach to the analysis of microvessel structure and hematocrit distribution
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 52-60
Google Scholar

[11] [11]
Strahler A.N.
Quantitative analysis of watershed morphology
Trans Am Geophys Union, 38 (1957), pp. 913-920
Google Scholar

[12] [12]
TorresFilho I.P., Popel A.S., Johnson P.C., Cyrino F.Z.G.A., Bouskela E.
Shape and orientation of arterial loops in cat sartorius muscle
Int J Microcirc: Clin Exp, 9 (1990), pp. 297-302
Google Scholar

[13] [13]
Joyner W.L., Davis M.J., Gilmore J.P.
Intravascular pressure distribution and dimensional analysis of microvessels in hamsters with renovascular hypertension
Microvasc Res, 22 (1981), pp. 190-198
Google Scholar

[14] [14]
Kuo L., Davis M.J., Chilian W.M.
Myogenic activity in isolated subepicardial and subendocardial coronary arterioles
Am J Physiol, 255 (1988), pp. H1558-H1562
Google Scholar

[15] [15]
Sakai H., Hara H., Tsai A.G., Tsuchida E., Intaglietta M.
Constriction of resistance arteries determines l-NAME-induced hypertension in a conscious hamster model
Microvasc Res, 60 (2000), pp. 21-27
Google Scholar

[16] [16]
Rhodin J.A.G.
The ultrastructure of mammalian arterioles and precapillary sphincters
J Ultrastruct Res, 18 (1967), pp. 181-223
Google Scholar

[17] [17]
Schmid-Schoenbein G.W., Skalak T.C., Engelson E.T., Zweifach B.W.
Microvascular network anatomy in rat skeletal muscle
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 38-51
Google Scholar

[18] [18]
Sullivan S.M., Johnson P.C.
Effect of oxygen on arteriolar dimensions and blood flow in cat sartorius muscle
Am J Physiol, 241 (1981), pp. H547-H556
Google Scholar

[19] [19]
Smaje L., Zweifach B.W., Intaglietta M.
Micropressures and capillary filtration coefficients in single vessels of the cremaster muscle of the rat
Microvasc Res, 2 (1970), pp. 96-110
Google Scholar

[20] [20]
Chambers R., Zweifach B.W.
Topography and function of the mesenteric capillary circulation
Am J Anat, 75 (1944), pp. 173-206
Google Scholar

[21] [21]
Fuxe K., Sedvall G.
The distribution of adrenergic nerve fibres to the blood vessels in skeletal muscle
Acta Physiol Scand, 64 (1965), pp. 75-86
Google Scholar

[22] [22]
Dodd L.R., Johnson P.C.
Diameter changes in arteriolar networks of contracting skeletal muscle
Am J Physiol, 260 (1991), pp. H662-H670
Google Scholar

[23] [23]
Segal S.S.
Integration of blood flow control to skeletal muscle: key role of feed arteries
Acta Physiol Scand, 168 (2000), pp. 511-518
Google Scholar

[24] [24]
Emerson G.G., Segal S.S.
Electrical activation of endothelium evokes vasodilation and hyperpolarization along hamster feed arteries
Am J Physiol, 280 (2001), pp. H160-H167
Google Scholar

[25] [25]
Rhodin J.A.
Ultrastructure of mammalian venous capillaries, venules and small collecting veins
J Ultrastructure Res, 25 (1968), pp. 452-500
Google Scholar

[26] [26]
Majno G.
Ultrastructure of the vascular membrane
W.F. Hamilton (Ed.), Handbook of Physiology, Circulation, Vol. III, American Physiological Society, Washington, DC (1965), pp. 2293-2375
Chapter 64, Section 2
Google Scholar

[27] [27]
Reilly F.D., McCuskey R.S., Cilento E.V.
Hepatic microvascular regulatory mechanisms: I
Adrenergic mechanisms. Microvasc Res,, 21 (1981), pp. 103-116
Google Scholar

[28] [28]
Eriksson E., Mryhage R.
Microvascular dimensions and blood flow in skeletal muscle
Acta Physiol Scand, 86 (1972), pp. 211-222
Google Scholar

[29] [29]
Bassingthwaite J.B., Yipintsoi T., Harvey R.B.
Microvasculature of the dog left ventricular myocardium
Microvasc Res, 7 (1974), pp. 229-249
Google Scholar

[30] [30]
Altman P. Blood and Other Body Fluids, eds Ditmer D and Washington DC. FASEB, 1961, p. 119.
Google Scholar

[31] [31]
Ley K., Pries A.R., Gaehtgens P.
Topological structure of the rat mesenteric microvessel networks
Microvasc Res, 32 (1986), pp. 315-332
Google Scholar

[32] [32]
Clark E.R., Clark E.L.
Observations on living arterio-venous anastomoses as seen in transparent chambers introduced into the rabbit's ear
Am J Anat, 54 (1934), pp. 229-286
Google Scholar

[33] [33]
House S.D., Johnson P.C.
Diameter and blood flow of skeletal muscle venules during local flow regulation
Am J Physiol, 250 (1986), pp. H828-H837
Google Scholar

[34] [34]
Koller A., Dawant B., Popel A.S., Johnson P.C.
Quantitative analysis of arteriolar network architecture in cat sartorius muscle
Am J Physiol, 253 (1987), pp. H154-H164
Google Scholar

[35] [35]
Marshall J.M., Hebert M.T.
Differential effect of changes in sympathetic activity on consecutive sections of microcirculation of mesentery and skeletal muscle
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 123-133
Google Scholar

[36] [36]
Bohlen H.G., Gore R.W.
Comparison of microvascular pressures and diameters in the innervated and denervated rat intestine
Microvasc Res, 14 (1977), pp. 251-264
Google Scholar

[37] [37]
Pappenheimer J.R.
Contributions to microvascular research of Jean Leonard Marie Poiseulle
E.M. Renkin, C.C. Michel (Eds.), Handbook of Physiology, Section 2: The Cardiovascular System, Volume IV, American Physiological Society, Washington (1984)
Chapter 1, Microcirculation, Part 1
Google Scholar

[38] [38]
Mall J.P.
Die Blut und Lymphwege im Dunndarm des Hundes
Abhandlungen der mathematischphysischen Classe der konigl Sachischen Gesellschaft der Wissenschaften, 14 (3) (1887)
Google Scholar

[39] [39]
Schlier J.
Der energieverbrauch in der blutbahn
Pfluegers Archiv fuer die gesamte Physiologie des Menschen und der Tiere, 173 (1918), pp. 172-204
Google Scholar

[40] [40]
Green HD. “Medical Physics”, ed. Glasser O. Chicago: Year Book Publ, 1944.
Google Scholar

[41] [41]
Fronek K., Zweifach B.W.
Microvascular pressure distribution in skeletal muscle and the effect of vasodilatation
Am J Physiol, 228 (1975), pp. 791-796
Google Scholar

[42] [42]
Schmid-Schoenbein G.W., Muakami H.
Blood flow in contracting arterioles
Int J Microcirc Clin Exp, 4 (1981, 1985), pp. 311-328

[43] [43]
Johnson P.C.
Landis Award Lecture 1976. The myogenic response and the microcirculation
Microvasc Res, 13 (1977), pp. 1-18
Google Scholar

[44] [44]
Smiesko V., Lang D.J., Johnson P.C.
Dilator response of rat mesenteric arcading arterioles to increased flow
Am J Physiol, 257 (1989), pp. H1958-H1965
Google Scholar

[45] [45]
Christensen K.L., Mulvany M.J.
Location of resistance arteries
J Vasc Res, 38 (2001), pp. 1-12
Google Scholar

[46] [46]
Clifford P.S., Hellsten Y.
Vasodilatory mechanisms in contracting skeletal muscle
J Appl Physiol, 97 (2004), pp. 393-403
Google Scholar

[47] [47]
Hester R.L., Hammer L.W.
Venular-arteriolar communication in the regulation of blood flow
Am J Physiol, 282 (2002), pp. R1280-R1285
Google Scholar

[48] [48]
Tigno X.T., Ley K., Pries A.R., Gaehtgens P.
Venulo-arteriolar communication and propagated response. A possible mechanism for local control of blood flow
Pflugers Arch, 414 (1989), pp. 450-456
Google Scholar

[49] [49]
Zweifach B.W.
The structure and reaction of small blood vessels in amphibia
Am J Anat, 60 (1937), pp. 473-514
Google Scholar

[50] [50]
Clark E.R., Clark E.L.
Caliber changes in minute blood vessels observed in the living mammal
Am J Anat, 73 (1943), pp. 215-250
Google Scholar

[51] [51]
Gorcznski R.J., Klitzman B., Duling B.R.
Interrelations between contracting striated muscle and precapillary microvessels
Am J Physiol, 235 (1978), pp. H494-H504
Google Scholar

[52] [52]
Zweifach B.W.
The microcirculatory module, myth or reality?
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 1-11
Google Scholar

[53] [53]
Mayrovitz H.N.
Hemodynamic significance of microvascular arteriolar anastomosing
A.S. Popel, P.C. Johnson (Eds.), Microvascular Networks: Experimental and Theoretical Studies, Basel, Karger (1986), pp. 197-209
Google Scholar

[54] [54]
Renkin E.M.
Control of circulation and blood-tissue exchange (Chapter 14)
E.M. Renkin, C.C. Michel (Eds.), Handbook of Physiology, Section 2: The Cardiovascular System Vol IV Microcirculation, Part 2, American Physiological Society, Bethesda (1984)
Google Scholar

[55] [55]
Stromberg D.D., Fox J.R.
Pressures in the pial arterial microcirculation of the cat during changes in systemic arterial blood pressure
Circ Res, 31 (1972), pp. 229-239
Google Scholar

[56] [56]
Schretzenmayr A.
Uber kreislaufregulatorische Vorgange an den grossen Arterien bei der Muskelarbeit
Pfluegers Arch, 232 (1933), pp. 743-748
Google Scholar

[57] [57]
Hilton S.
A peripheral arterial conducting mechanism underlying dilation of the femoral artery and concerned in functional vasodilatation in skeletal muscle
J Physiol Lond, 149 (1959), pp. 93-111
Google Scholar

[58] [58]
Khayutin V., Melkumyants A.M., Rogoza A.N., Veselova E.S., Balashov S.A., Nikolsky V.P.
Flow-induced control of the arterial lumen
Acta Physiol Hung, 68 (1986), pp. 241-251
Google Scholar

[59] [59]
Rubanyi G.M., Romero C.J., Vanhoutte P.M.
Flow-induced release of endothelium-derived relaxing factor
Am J Physiol, 250 (1986), pp. H1145-H1149
Google Scholar

[60] [60]
Pries A.R., Secomb T.W., Jacobs H., Sperandio M., Osterloh K., Gaehtgens P.
Microvascular flow resistance: role of endothelial surface layer
Am J Physiol, 273 (1997), pp. H2272-H2279
Google Scholar

[61] [61]
Cabel M., Meiselman H.J., Popel A.S., Johnson P.C.
Contribution of red blood cell aggregation to venous vascular resistance in skeletal muscle
Am J Physiol, 272 (1997), pp. H1020-H1032
Google Scholar

[62] [62]
Kuo L., Arko F., Chilian W.M., Davis M.J.
Coronary venular responses to flow and pressure
Circ Res, 72 (1993), pp. 607-615
Google Scholar

[63] [63]
Bishop J.J., Nance P.R., Popel A.S.
Intaglietta M and Johnson PC
Diameter changes in skeletal muscle venules during arterial pressure reduction. Am J Physiol,, 279 (2000), pp. H47-H57
Google Scholar

[64] [64]
Laughlin H.M., Joyner M.
Closer to the edge? Contractions, pressures, waterfalls and blood flow to contracting skeletal muscle
J Appl Physiol, 94 (2003), pp. 3-5
Google Scholar

[65] [65]
Krogh A.
Supply of oxygen to the tissues and the regulation of the capil1ary circulation
J Physiol (Lond), 52 (1919), pp. 457-474
Google Scholar

[66] [66]
Duling B.R., Berne R.M.
Longitudinal gradients in periarteriolar oxygen tension: Possible mechanism for the participation of oxygen in local regulation of blood flow
Circ Res, 27 (1970), pp. 669-678
Google Scholar

[67] [67]
Tsai A.G., Friesnecker B., Mazzoni M.D., Kerger H., Buerk D.G., Johnson P.C., Intaglietta M.
Microvascular and tissue oxygen gradients in the rat mesentery
Proc Natl Acad Sci USA, 95 (1998), pp. 6590-6595
Google Scholar

[68] [68]
Tsai A.G., Johnson P.C., Intaglietta M.
Oxygen gradients in the microcirculation
Physiol Rev, 83 (2003), pp. 933-963
Google Scholar

[69] [69]
Wagner P.D.
Diffusional resistance to O2 transport in muscle
Acta Physiol Scand, 168 (2000), pp. 609-614
Google Scholar

[70] [70]
Starling E.
On the absorption of fluids from the connective tissue spaces
J Physiol (Lond), 19 (1896), pp. 312-326
Google Scholar

[71] [71]
Landis E.M.
Mirco-injection studies of capillary permeability: II the relation between capillary pressure and the rate at which fluid passes through the walls of single capillaries
Am J Physiol, 82 (1927), pp. 217-238
Google Scholar

[72] [72]
Pappenheimer J.R., Soto Rivera A.
Effective osmotic pressure of the plasma proteins and other quantities associated with the capillary circulation in the hindlimbs of cats and dogs
Am J Physiol, 152 (1948), pp. 471-491
Google Scholar

[73] [73]
Guyton A.C.
A concept of negative interstitial pressure based on pressures in implanted perforated capsules
Circ Res, 12 (1963), pp. 399-414
Google Scholar

[74] [74]
Wiederhielm C.A., Weston B.V.
Microvascular, lymphatic and tissue pressures in the unanesthetized mammal
Am J Physiol, 225 (1973), pp. 992-996
Google Scholar

[75] [75]
Johnson P.C.
Effect of venous pressure on mean capillary pressure and vascular resistance in the intestine
Circ Res, 16 (1965), pp. 294-300
Google Scholar

[76] [76]
Mortillaro N.A., Taylor A.E.
Interaction of capillary and tissue forces in the cat small intestine
Circ Res, 39 (1976), pp. 348-358
Google Scholar

[77] [77]
Chambers R., Zweifach B.W.
Intercellular cement and capillary permeability
Physiol Rev, 27 (1947), pp. 436-463
Google Scholar

[78] [78]
Pappenheimer J.R., Renkin E.M., Borrero J.M.
Filtration, diffusion and molecular sieving through peripheral capillary membranes. A contribution to the pore theory of capillaray permeability
Am J Physiol, 167 (1951), pp. 13-46
Google Scholar

[79] [79]
Michel C.C., Curry F.E.
Microvascular permeability
Physiol Rev, 79 (1999), pp. 703-761
Google Scholar

[80] [80]
Levick J.R.
Capillary filtration-absorption balance reconsidered in light of dynamic extravascular factors
Exp Physiol, 76 (1991), pp. 825-857
Google Scholar

[81] [81]
Wolf M.D., Watson P.D.
Measurement of osmotic reflection coefficient for small molecules in cat hindlimbs
Am J Physiol, 256 (1989), pp. H282-H290
Google Scholar

[82] [82]
Grotte G.
Passage of dextran molecules across the blood-lymph barrier
Acta Chir Scand, 211 (Suppl.) (1956), pp. 1-84
Google Scholar

[83] [83]
Palade G.E.
Transport in quanta across the endothelium of blood capillaries
Anat Rec, 136 (1960), p. 254
(abstract)
Google Scholar

[84] [84]
Majno G., Palade G.E., Schoefl G.
Studies on inflammation II. The site of action of histamine and serotonin along the vascular tree: a topographic study
J Biophys Biochem Cytol, 11 (1961), pp. 607-626
Google Scholar

[85] [85]
Yuan Y., Chilian W.M., Granger H.J., Zaweija D.C.
Flow modulates coronary venular permeability by a nitric oxide-related mechanism
Am J Physiol, 263 (1992), pp. H641-H646
Google Scholar

[86] [86]
Dutrochet H.
Recherches anatomiques et physiologiques sur la structure intime des animaux et des végetaux, et sur leur motilité
Bailliere et fils, Paris (1824)
Google Scholar

[87] [87]
Ohashi K.L., Tung K-L., Wilson J., Zweifach B.W., Schmid-Schoenbein G.
Transvascular and Interstitial migration of neutrophils in rat mesentery
Microcirculation, 3 (1996), pp. 199-210
Google Scholar

[88] [88]
Tsai M.A., Frank R.S., Waugh R.E.
Passive mechanical behavior of human neutrophils: power-law fluid
Biophys J, 65 (1994), pp. 2078-2088
Google Scholar

[89] [89]
Burns A.R., Walker D.C., Brown E.S., Thurmon L.T., Bowden R.A., Keese C.R., Simon S.I., Entman M.L., Smith C.W.
Neutrophil transendothelial migration is independent of tight junctions and occurs preferentially at tricellular corners
J Immunol, 159 (1997), pp. 2893-2903
Google Scholar

[90] [90]
Damon D.H., Duling B.R.
Distribution of capillary blood flowin the microcirculation of the hamster. An in vivo study using epifluorescent microscopy
Microvasc Res, 27 (1984), pp. 81-95
Google Scholar

[91] [91]
Unthank J.L., Lash J.M., Nixon J., Snider R.A., Bohlen H.G.
Evaluation of carbocyanine-labeled erythrocytes for microvascular measurements
Microvasc Res, 45 (1993), pp. 193-210
Google Scholar

[92] [92]
Tangelder G.J., Slaaf D.W., Muijtjens A.M.M., Arts T.
oude Egbrink MGA and Reneman RS. Velocity profiles of blood platelets and red blood cells flowing in arterioles of the rabbit mesentery
Circ Res, 59 (1986), pp. 505-514
Google Scholar

[93] [93]
Paques M., Boval B., Richard S., Tadayoni R., Massin P., Mundler O., Gaudric A., Vicaut E.
Evaluation of fluorescein-labeled autologous leukocytes for examination of retinal circulation in humans
Curr Eye Res, 21 (2000), pp. 560-565
Google Scholar

[94] [94]
Adamson R.H., Lenz J.F., Curry F.E.
Quantitative laser scanning confocal microscopy on single capillaries: permeability measurement
Microcirculation, 1 (1994), pp. 251-265
Google Scholar

[95] [95]
Chaigneau E., Oheim M., Audinat E., Charpak S.
Two-photon imaging of capillary blood flow in olfactory bulb glomeruli
Proc Natl Acad Sci USA, 100 (2003), pp. 13081-13086
Google Scholar

[96] [96]
Beacham W.S., Konishi A., Hunt C.C.
Observations of the microcirculatory bed in rat mesocecum using differential interference contrast microscopy in vivo and electron microscopy
Am J Anat, 146 (1976), pp. 385-425
Google Scholar

[97] [97]
Trache A., Meininger G.A.
Atomic force-multi-optical imaging integrated microscope for monitoring molecular dynamics in live cells
J Biomed Opt, 10 (2005)
064023
Google Scholar

[98] [98]
Messmer K., Sunder-Plassmann L., Jesch F., Gornandt L., Sinagowitz E., Kessler M.
Oxygen supply to the tissues during limited normovolemic hemodilution
Res Exp Med (Berl), 159 (1973), pp. 152-166
Google Scholar

[99] [99]
Whalen W.J., Riley J., Nair P.
Microelectrode for measuring intracellular PO2
J Appl Physiol, 23 (1967), pp. 798-801
Google Scholar

[100] [100]
Lund N., Sjoberg F., Guldbrand H., Walfridsson H., Edwall G.
A multipoint micro antimony pH electrode for tissue surface measurements
Int J Clin Monit Comput, 1 (1984), pp. 147-153
Google Scholar

[101] [101]
Bohlen H.G.
Mechanism of increased vessel wall nitric oxide concentrations during intestinal absorption
Am J Physiol, 275 (1998), pp. H542-H550
Google Scholar

[102] [102]
Buerk D.G., Riva C.E., Cranstoun
Nitric oxide has a vasodilatory role in cat optic nerve head during flicker stimuli
Microvasc Res, 52 (1996), pp. 13-26
Google Scholar

[103] [103]
Pittman R.N.
Microvessel blood oxygen measurement techniques
C.H. Baker, W.L. Nastuk (Eds.), Microcirulatory Technology, Academic, Orlando Fl (1987), pp. 367-390
Google Scholar

[104] [104]
Mayhan W.G.
Nitric oxide accounts for histamine-induced increases in macromolecular extravasation
Am J Physiol, 266 (1994), pp. H2369-H2373
Google Scholar

[105] [105]
Wilson D.F.
Measuring oxygen using oxygen dependent quenching of phosphorescence: A status report
Adv Exp Med Bio, 333 (1993), pp. 225-232
Google Scholar

[106] [106]
Zheng L., Golub A.S., Pittman R.N.
Determination of pO2 and its heterogeneity in single capillaries
Am J Physiol, 271 (1996), pp. H365-H372
Google Scholar

[107] [107]
Torres Filho I.P., Intaglietta M.
Microvessel pO2 measurements by phosphorescence decay method
Am J Physiol, 265 (1993), pp. H1434-H1438
Google Scholar

[108] [108]
Buerk D.G., Tsai A.G., Intaglietta M., Johnson P.C.
In vivo tissue pO₂ measurements in hamster skinfold by recessed pO₂ microelectrodes and phosphorescence quenching are in agreement
Microcirculation, 5 (1998), pp. 219-225
Google Scholar

[109] [109]
Toth A., Tischler M.E., Pal M., Koller A., Johnson P.C.
A multipurpose instrument for quantitative intravital microscopy
J Appl Physiol, 73 (1992), pp. 296-306
Google Scholar

[110] [110]
Loutzenhiser R.D.
In situ studies of renal arteriolar function using the in vitro-perfused hydronephrotic rat kidney
Int Rev Exp Pathol, 36 (1996), pp. 145-160
Google Scholar

[111] [111]
Munro P.A.G.
Methods for measuring the velocity of moving particles under the microscope
R. Barer, V.E. Cosslett (Eds.), Advances in Optical and Electron Microscopy, vol. 1, Academic, New York (1966), pp. 1-40
Google Scholar

[112] [112]
Bloch E.H.
Quantitative study of the hemodynamics in the living microvascular system
Am J Anat, 110 (1962), pp. 125-153
Google Scholar

[113] [113]
Intaglietta M., Tompkins W.R.
On-line measurement of microvascular dimensions by television microscopy
J Appl Physiol, 32 (1983), pp. 546-551
Google Scholar

[114] [114]
Wayland H., Johnson P.C.
Erythrocyte velocity measurement in microvessels by a two-slit photometric method
J Appl Physiol, 22 (1967), pp. 333-337
Google Scholar

[115] [115]
Intaglietta M., Tompkins W.R.
System for the measurement of velocity of microscopic particles in liquids
IEEE Trans Biomed, 18 (1971), pp. 376-377
Google Scholar

[116] [116]
Baker M., Wayland H.
On-line volume flow rate velocity profile measurement for blood in microvessels
Microvasc Res, 7 (1974), pp. 131-143
Google Scholar

[117] [117]
Davis M.J.
Determination of volumetric flow in capillary tubes using an optical Doppler velocimeter
Microvasc Res, 34 (1987), pp. 223-230
Google Scholar

[118] [118]
Bishop J.J., Nance P.R., Popel A.S., Intaglietta M., Johnson P.C.
Relationship between erythrocyte aggregate size and flow rate in skeletal muscle venules
Am J Physiol, 286 (2004), pp. H113-H120
Google Scholar

[119] [119]
Sarelius I.H., Duling B.R.
Direct measurement of microvessel hematocrit, red cell flux, velocity and transit time
Am. J. Physiol, 243 (1982), pp. H1018-H1026
Google Scholar

[120] [120]
Bishop J.J., Nance P.R., Popel A.S., Intaglietta M., Johnson P.C.
Effect of erythrocyte aggregation on velocity profiles in venules
Am. J. Physiol, 280 (2001), pp. H222-H236
Google Scholar

[121] [121]
Smith M.L., Long D.S., Damiano E.R., Ley K.
Near wall PIV reveals a hydrodynamically relevant endothelial surface layer in venules in vivo
Biophys. J, 85 (2003), pp. 637-645
Google Scholar

[122] [122]
Roy C.S., Brown J.G.
The blood pressure and its variations in the arterioles, capillaries and veins
J. Physiol (Lond), 2 (1880), pp. 323-359
Google Scholar

[123] [123]
Landis E.M.
The capillary pressure in frog mesentery as determined by micro-injection methods
Am J Physiol, 75 (1926), pp. 548-570
Google Scholar

[124] [124]
Wiederhielm C.A., Woodbury J.W., Kirk S., Rushmer R.F.
Pulsatile pressures in the microcirculation of the frog's mesentery
Am J Physiol, 207 (1964), pp. 173-176
Google Scholar

[125] [125]
Intaglietta M., Tompkins W.R.
Micropressure measurement with 1 micron and smaller cannulae
Microvasc Res, 3 (1971), pp. 211-214
Google Scholar

[126] [126]
Segal S.S., Beny J.L.
Intracellular recording and dye transfer in arterioles during blood flow control
Am J Physiol, 263 (1992), pp. H1-H7
Google Scholar

[127] [127]
Beach J.M., McC\Gahren E.F., Xia J., Duling B.R.
Ratiometric measurement of endothelial depolarization in arterioles with a potential-sensitive dye
Am J Physiol, 270 (1996), pp. H2216-H2227
Google Scholar

[128] [128]
Nicoll P.A., Webb R.L.
Vascular patterns and active vasomotion as determiners of flow through minute vessels
Angiology, 6 (1955), pp. 291-308
Google Scholar

[129] [129]
Microcirculatory Research Methods. Microvascular Research 5: 229–435, 1973.
Google Scholar

[130] [130]
Baez S.
An open cremaster muscle preparation for the study of blood vessels by in vivo microscopy
Microvasc Res, 5 (1973), pp. 384-394
Google Scholar

[131] [131]
Hill M.A., Simpson B.E., Meininger G.A.
Altered cremaster muscle hemodynamics due to disruption of the deferential feed vessels
Microvasc Res, 39 (1990), pp. 349-363
Google Scholar

[132] [132]
Gore R.W.
Mesenteric preparations for quantitative microcirculatory studies
Microvasc Res, 5 (1973), pp. 368-375
Google Scholar

[133] [133]
Frasher W.G. Jr.
Attached floating cat mesentery preparation for vital microscopy
Microvasc Res, 5 (1973), pp. 376-383
Google Scholar

[134] [134]
Gray S.D.
Rat spinotrapezius muscle preparation for microscopic observation of the terminal vascular bed
Microvasc Res, 5 (1973), pp. 395-400
Google Scholar

[135] [135]
Klotz K.F., Pries A.R., Jepsen H., Gossrau R., Gaehtens P.
A new approach to videomicroscopy of rat spinotrapezius muscle
Int J Microcirc Clin Exp, 10 (1991), pp. 205-218
Google Scholar

[136] [136]
Zweifach B.W., Intaglietta M.
Mechanics of fluid movement across single capillaries in the rabbit
Microvasc Res, 1 (1968), pp. 83-101
Google Scholar

[137] [137]
Lindbom L., Arfors K.E.
Mechanisms and site of control for variation in the number of perfused capillaries in skeletal muscle
Int J Microcirc Clin Exp, 4 (1985), pp. 19-30
Google Scholar

[138] [138]
Burton K.M.
Cat sartorius muscle: an istolated perfused skeletal muscle preparation for microvascular research
Microvasc Res, 5 (1973), pp. 401-409
Google Scholar

[139] [139]
Stromberg D.D., Shapiro H.M.
Preparation of the cat cerebral cortical surface for microvascular pressure measurements
Microvasc Res, 5 (1973), pp. 410-416
Google Scholar

[140] [140]
Duling B.R.
The preparation and use of the hamster cheek pouch for studies of the microcirculation
Microvasc Res, 5 (1973), pp. 423-429
Google Scholar

[141] [141]
Sullivan S.M., Pttman R.N.
Hamster retractor muscle: a new preparation for intravital microscopy
Microvasc Res, 23 (1982), pp. 329-335
Google Scholar

[142] [142]
Wiedeman M.P.
Preparation of the bat wing for in vivo microscopy
Microvasc Res, 5 (1973), pp. 417-422
Google Scholar

[143] [143]
Papenfuss H.D., Gross J.F., Intaglietta M., Treese F.A.
A transparent access chamber for the rat dorsal skin fold
Microvasc Res, 18 (1979), pp. 311-318
Google Scholar

[144] [144]
Endrich B., Asaishi K., Götz A., Messmer K.
Technical report – a new chamber technique for microvascular studies in unanesthetized hamsters
Res Exp Med (Berl), 177 (1980), pp. 125-134
Google Scholar

[145] [145]
Menger M.D., Jäger S., Walter P., Hammersen F., Messmer K.
A novel technique for studies on the microvasculature of transplanted islets of Langerhans in vivo
Int J Microcirc Clin Exp, 9 (1990), pp. 103-117
Google Scholar

[146] [146]
Wiedeman M.P.
Patterns of the arteriovenous pathways
W.F. Hamilton, P. Dow, D.C. Washington (Eds.), Handbook of Physiology, vol. 11, American Physiological Society (1963), pp. 891-933
section 2
Google Scholar

[147] [147]
Carpentier P., Franco A.
L'angioscopie conjunctivale DELTACOM
Boulogne-billancourt, France (1985)
Google Scholar

[148] [148]
Fagrell B., Fronek A., Intaglietta M.
A microscope-television system for studying flow velocity in human skin capillaries
Am J Physiol, 233 (1977), pp. H318-H321
Google Scholar

[149] [149]
Seifert H., Jäger K., Bollinger A.
Laser-Doppler probes for the evaluation of arterial ischemia
Adv Exp Med Biol, 220 (1987), pp. 227-229
Google Scholar

[150] [150]
Slaaf D.W., Tangelder G.J., Reneman R.S., Jager K., Bollinger A.
A versatile incident illuminator for intravital microcscopy
Int J Microcirc Clin Exp, 6 (1987), pp. 391-397
Google Scholar

[151] [151]
Mathura K.R., Vollebregt K.C., Boer K., De Graaff J.C., Ubbink D.T., Ince C.
Comparison of OPS imaging and conventional capillary microscopy to study the human microcirculation
J Appl Physiol, 91 (2001), pp. 74-78
Google Scholar

[152] [152]
Huch A., Franzeck U.K., Huch R., Bollinger A.
A transparent transcutaneous oxygen electrode for simultaneous studies of skin capillary morphology, flow dynamics and oxygenation
Int J Microcirc Clin Exp, 2 (1983), pp. 103-108
Google Scholar

[153] [153]
Kubli S., Waeber B., Dalle-Ave A., Feihl F.
Reproducibility of laser Doppler imaging of skin blood flow as a tool to assess endothelial function
J Cardiovasc Pharmacol, 36 (2000), pp. 640-648
Google Scholar