Elsevier

Brain Research

Volume 934, Issue 1, 26 April 2002, Pages 1-6
Brain Research

Research report
Exercise induces angiogenesis but does not alter movement representations within rat motor cortex

https://doi.org/10.1016/S0006-8993(02)02239-4Get rights and content

Abstract

The effects of exercise on the topography of movement representations and blood vessel density within the rat forelimb motor cortex was examined. Adult male rats were allocated to either a Voluntary eXercise (VX) or Inactive Condition (IC). VX animals were housed for 30 days with unlimited access to running wheels while IC animals were housed in standard laboratory cages. VX animals exhibited a progressive increase in the distance traveled per day and ran an average of 58.3 km across the 30-day training period. Microelectrode stimulation was used to derive high resolution maps of the forelimb representations within the motor cortex of animals from both conditions. No significant differences in the area of either distal (wrist/digit) or proximal (elbow/shoulder) movement representations were found between VX and IC animals. However, VX animals did have a significantly greater density of blood vessels within layer V of the forelimb motor cortex. These results demonstrate that increases in forelimb motor activity sufficient to induce cortical angiogenesis does not alter the topography of forelimb movement representations within forelimb motor cortex.

Introduction

The existence of a motor map within mammalian motor cortex has been known for over a century [12]. Early experiments demonstrated that although general map topography was consistent between animals, the size and organization of individual maps was unstable [38]. The capacity for motor map reorganization has now been demonstrated to occur in response to a variety of manipulations including changes in sensory input [8], [18], administration of GABA antagonists [20] and repetitive electrical stimulation [29]. It has been hypothesized that motor map plasticity exists to support the acquisition of novel motor behaviors [37]. Specifically, the development of skilled action patterns causes an expansion of representations corresponding to trained movements into areas occupied by untrained representations [11], [22], [31], [34]. Further, this plasticity also appears to be learning-dependent and does not occur in response to the simple repetition of existing, unskilled movement patterns [23], [22], [34].

Although the topography of movement representations within motor cortex may reflect the capacity for skilled motor behavior [24], [30], [34], there is evidence that training-dependent increases in motor endurance may also influence cortical function. Extensive exercise training has been shown not only to increase local glucose utilization [40] but also the capacity for glucose utilization within motor cortex [26]. In addition, persistent changes in the density of various neurotransmitter receptors [9], [10], [27] and prolonged increases in neurotransmitter release [7], [16], [32] have been reported within frontal cortex following exercise training. An increase in norepinephrine [32] and NE receptors [30] is consistent with an increase in cortical vasculature given that most NE afferents to the cortex terminate within the vicinity of microvessels [17]. Further, release of various neurotrophic factors [28] and the density of FLK-1 receptors within the cortex [5] have also been shown to increase with exercise. The persistent increase in activity and concomitant neurochemical changes observed within motor cortex following exercise training likely reflect changes in cortical vasculature and physiology. The present experiment examined how exercise affected both the topography of movement representations and the density of blood vessels within the rat forelimb motor cortex.

Section snippets

Motor training

Sixteen male Long-Evans hooded rats approximately 5 months of age (450–550 g) were randomly assigned to either a Voluntary eXercise (VX) condition or an Inactive Control (IC) condition, with littermates equally distributed across condition. Animals in the VX group (n=8) had free access to a running wheel (36 cm in diameter) attached to their home cages. The number of wheel rotations was recorded and used to calculate distance traveled per day over 30 days. VX animals also had constant access to

Exercise training

A within subject analysis of variance (ANOVA) revealed a significant effect of TIME on distance traveled per day in the VX animals (F(7,35)=2.99; P<0.05) (Fig. 1). The mean distance traveled per day progressively increased across the 30-day training period suggesting an increased capacity to sustain running wheel activity. A mean total of 58.3 (±4.6) km across the 30-day training period which is comparable to previously obtained values in similar experiments [1], [19].

Movement representations

The total area of the CFA

Discussion

Adaptations of motor behavior brought about through differential motor experience appear to be supported by adaptations in the structure and function of the motor system. Further, the nature of the adaptation is dictated by the specific behavioral demands imposed by a motor training experience. For example, the development of motor skill is associated with changes in neuron morphology [15], [24], [21], synaptic strength [35], [36] and topography of movement representations within motor cortex

Summary

In summary, animals exposed to running wheels exhibited a progressive increase in the distance traveled per day across a 30-day training period. Despite this chronic increase in motor activity, no differences in the size or topography of movement representations within motor cortex were observed in comparison to inactive controls. However, exercised animals did exhibit a significant increase in the density of blood vessels within layer V of physiologically defined motor cortex. These results

Acknowledgements

The authors acknowledge Bryan Kolb for his thoughtful comments on the manuscript. This work was supported by grants to JAK from Natural Sciences and Engineering Research Council, Medical Research Council of Canada, Alberta Heritage Foundation for Medical Research and the Canada Foundation for Neuroscience.

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