Literature DB >> 3337250

Effect of sciatic nerve stimulation on pial arterioles in rats.

A C Ngai1, K R Ko, S Morii, H R Winn.   

Abstract

The present study documents the microvascular response of the pial circulation in sensory hindlimb cortex to sciatic nerve stimulation. Rats, anesthetized with alpha-chloralose and urethan, were equipped with closed cranial windows, and pial arteriolar diameter was measured during stimulation of the contralateral sciatic nerve. The effects of varying stimulus frequency, intensity, and duration were examined. Optimal stimulus frequency was 5 Hz, but response diminished significantly beyond 10 Hz. Optimal stimulus intensity was 0.2 V. At higher stimulus strength, arteriolar dilation was reduced, but systemic blood pressure rose significantly. At low stimulus frequency and intensities, pial arterioles responded to stimulation with a consistent pattern: initial delay of 1.4 s followed by abrupt dilation to a peak magnitude, subsequent decline to a lesser but still dilated state, and recovery to a resting diameter after the cessation of stimulation. No consistent response profile was discernible at high stimulus intensity and/or frequency. This vasodilatory response was discretely restricted to a limited number of arterioles, confined to the hindlimb somatosensory cortex as confirmed by sensory evoked response. The response of the pial circulation provides a well-characterized model for analysis of brain microcirculation, which presumably is linked to cerebral metabolism.

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Year:  1988        PMID: 3337250     DOI: 10.1152/ajpheart.1988.254.1.H133

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  23 in total

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Journal:  J Cereb Blood Flow Metab       Date:  2012-02-01       Impact factor: 6.200

3.  Resting cerebral blood flow alterations in chronic traumatic brain injury: an arterial spin labeling perfusion FMRI study.

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4.  Magnetic resonance imaging (MRI) detection of the murine brain response to light: temporal differentiation and negative functional MRI changes.

Authors:  W Huang; I Plyka; H Li; E M Eisenstein; N D Volkow; C S Springer
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

Review 5.  Cell-cell signaling in the neurovascular unit.

Authors:  Josephine Lok; Punkaj Gupta; Shuzhen Guo; Woo Jean Kim; Michael J Whalen; Klaus van Leyen; Eng H Lo
Journal:  Neurochem Res       Date:  2007-04-25       Impact factor: 3.996

Review 6.  The Neurovascular Unit Coming of Age: A Journey through Neurovascular Coupling in Health and Disease.

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Journal:  Neuron       Date:  2017-09-27       Impact factor: 17.173

7.  Fundamental increase in pressure-dependent constriction of brain parenchymal arterioles from subarachnoid hemorrhage model rats due to membrane depolarization.

Authors:  Matthew A Nystoriak; Kevin P O'Connor; Swapnil K Sonkusare; Joseph E Brayden; Mark T Nelson; George C Wellman
Journal:  Am J Physiol Heart Circ Physiol       Date:  2010-12-10       Impact factor: 4.733

8.  Hemodynamic scaling of fMRI-BOLD signal: validation of low-frequency spectral amplitude as a scalability factor.

Authors:  Bharat B Biswal; Sridhar S Kannurpatti; Bart Rypma
Journal:  Magn Reson Imaging       Date:  2007-05-04       Impact factor: 2.546

9.  Competitive inhibition of nitric oxide synthase prevents the cortical hyperemia associated with peripheral nerve stimulation.

Authors:  F J Northington; G P Matherne; R M Berne
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-15       Impact factor: 11.205

Review 10.  Regulation of cerebral vasculature in normal and ischemic brain.

Authors:  Tobias Kulik; Yoshikazu Kusano; Shimon Aronhime; Adam L Sandler; H Richard Winn
Journal:  Neuropharmacology       Date:  2008-04-26       Impact factor: 5.250

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