Modulation of cardiovascular excitatory responses in rats by transcutaneous magnetic stimulation: role of the spinal cord

1 Department of Medicine, Susan Samueli Center for Integrative Medicine and 2 Spinal Cord Injury/Disorder Health Care Group, Department of Physical Medicine and Rehabilitation, College of Medicine, University of California, Irvine, California Submitted 12 September 2005 ; accepted in final form 27 O...

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Veröffentlicht in:Journal of applied physiology (1985) 2006-03, Vol.100 (3), p.926-932
Hauptverfasser: Zhou (Yi Syuu), Wei, Hsiao, Ian, Lin, Vernon W. H, Longhurst, John C
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creator Zhou (Yi Syuu), Wei
Hsiao, Ian
Lin, Vernon W. H
Longhurst, John C
description 1 Department of Medicine, Susan Samueli Center for Integrative Medicine and 2 Spinal Cord Injury/Disorder Health Care Group, Department of Physical Medicine and Rehabilitation, College of Medicine, University of California, Irvine, California Submitted 12 September 2005 ; accepted in final form 27 October 2005 This study investigated the efficacy of magnetic stimulation on the reflex cardiovascular responses induced by gastric distension in anesthetized rats and compared these responses to those influenced by electroacupuncture (EA). Unilateral magnetic stimulation (30% intensity, 2 Hz) at the Jianshi-Neiguan acupoints (pericardial meridian, P 5–6) overlying the median nerve on the forelimb for 24 min significantly decreased the reflex pressor response by 32%. This effect was noticeable by 20 min of magnetic stimulation and continued for 24 min. Median nerve denervation abolished the inhibitory effect of magnetic stimulation, indicating the importance of somatic afferent input. Unilateral EA (0.3–0.5 mA, 2 Hz) at P 5–6 using similar durations of stimulation similarly inhibited the response (35%). The inhibitory effects of EA occurred earlier and were marginally longer (20 min) than magnetic stimulation. Magnetic stimulation at Guangming-Xuanzhong acupoints (gallbladder meridian, GB 37–39) overlying the superficial peroneal nerve on the hindlimb did not attenuate the reflex. Intravenous naloxone immediately after termination of magnetic stimulation reversed inhibition of the cardiovascular reflex, suggesting involvement of the opioid system. Also, intrathecal injection of - and -opioid receptors antagonists, ICI174,864 ( n = 7) and nor -binaltorphimine ( n = 6) immediately after termination of magnetic stimulation reversed inhibition of the cardiovascular reflex. In contrast, the µ-opioid antagonist CTOP ( n = 7) failed to alter the cardiovascular reflex. The endogenous neurotransmitters for - and -opioid receptors, enkephalins and dynorphin but not -endorphin, therefore appear to play significant roles in the spinal cord in mediating magnetic stimulation-induced modulation of cardiovascular reflex responses. magnetic field; cardiovascular response; noninvasive stimulation; naloxone; electroacupuncture Address for reprint requests and other correspondence: W. Zhou (Y. Syuu), Medical Science 1 C240, College of Medicine, Univ. of California, Irvine, CA 92697-4075 (e-mail: wzhou2{at}uci.edu )
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H ; Longhurst, John C</creator><creatorcontrib>Zhou (Yi Syuu), Wei ; Hsiao, Ian ; Lin, Vernon W. H ; Longhurst, John C</creatorcontrib><description>1 Department of Medicine, Susan Samueli Center for Integrative Medicine and 2 Spinal Cord Injury/Disorder Health Care Group, Department of Physical Medicine and Rehabilitation, College of Medicine, University of California, Irvine, California Submitted 12 September 2005 ; accepted in final form 27 October 2005 This study investigated the efficacy of magnetic stimulation on the reflex cardiovascular responses induced by gastric distension in anesthetized rats and compared these responses to those influenced by electroacupuncture (EA). Unilateral magnetic stimulation (30% intensity, 2 Hz) at the Jianshi-Neiguan acupoints (pericardial meridian, P 5–6) overlying the median nerve on the forelimb for 24 min significantly decreased the reflex pressor response by 32%. This effect was noticeable by 20 min of magnetic stimulation and continued for 24 min. Median nerve denervation abolished the inhibitory effect of magnetic stimulation, indicating the importance of somatic afferent input. Unilateral EA (0.3–0.5 mA, 2 Hz) at P 5–6 using similar durations of stimulation similarly inhibited the response (35%). The inhibitory effects of EA occurred earlier and were marginally longer (20 min) than magnetic stimulation. Magnetic stimulation at Guangming-Xuanzhong acupoints (gallbladder meridian, GB 37–39) overlying the superficial peroneal nerve on the hindlimb did not attenuate the reflex. Intravenous naloxone immediately after termination of magnetic stimulation reversed inhibition of the cardiovascular reflex, suggesting involvement of the opioid system. 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H</creatorcontrib><creatorcontrib>Longhurst, John C</creatorcontrib><title>Modulation of cardiovascular excitatory responses in rats by transcutaneous magnetic stimulation: role of the spinal cord</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>1 Department of Medicine, Susan Samueli Center for Integrative Medicine and 2 Spinal Cord Injury/Disorder Health Care Group, Department of Physical Medicine and Rehabilitation, College of Medicine, University of California, Irvine, California Submitted 12 September 2005 ; accepted in final form 27 October 2005 This study investigated the efficacy of magnetic stimulation on the reflex cardiovascular responses induced by gastric distension in anesthetized rats and compared these responses to those influenced by electroacupuncture (EA). Unilateral magnetic stimulation (30% intensity, 2 Hz) at the Jianshi-Neiguan acupoints (pericardial meridian, P 5–6) overlying the median nerve on the forelimb for 24 min significantly decreased the reflex pressor response by 32%. This effect was noticeable by 20 min of magnetic stimulation and continued for 24 min. Median nerve denervation abolished the inhibitory effect of magnetic stimulation, indicating the importance of somatic afferent input. Unilateral EA (0.3–0.5 mA, 2 Hz) at P 5–6 using similar durations of stimulation similarly inhibited the response (35%). The inhibitory effects of EA occurred earlier and were marginally longer (20 min) than magnetic stimulation. Magnetic stimulation at Guangming-Xuanzhong acupoints (gallbladder meridian, GB 37–39) overlying the superficial peroneal nerve on the hindlimb did not attenuate the reflex. Intravenous naloxone immediately after termination of magnetic stimulation reversed inhibition of the cardiovascular reflex, suggesting involvement of the opioid system. Also, intrathecal injection of - and -opioid receptors antagonists, ICI174,864 ( n = 7) and nor -binaltorphimine ( n = 6) immediately after termination of magnetic stimulation reversed inhibition of the cardiovascular reflex. In contrast, the µ-opioid antagonist CTOP ( n = 7) failed to alter the cardiovascular reflex. The endogenous neurotransmitters for - and -opioid receptors, enkephalins and dynorphin but not -endorphin, therefore appear to play significant roles in the spinal cord in mediating magnetic stimulation-induced modulation of cardiovascular reflex responses. magnetic field; cardiovascular response; noninvasive stimulation; naloxone; electroacupuncture Address for reprint requests and other correspondence: W. Zhou (Y. Syuu), Medical Science 1 C240, College of Medicine, Univ. of California, Irvine, CA 92697-4075 (e-mail: wzhou2{at}uci.edu )</description><subject>Afferent Pathways - physiology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Cardiovascular Physiological Phenomena</subject><subject>Cardiovascular system</subject><subject>Cardiovascular System - drug effects</subject><subject>Cardiovascular System - innervation</subject><subject>Electroacupuncture</subject><subject>Enkephalin, Leucine - analogs &amp; derivatives</subject><subject>Enkephalin, Leucine - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Magnetics</subject><subject>Magnetism</subject><subject>Male</subject><subject>Median Nerve - physiology</subject><subject>Naloxone - pharmacology</subject><subject>Neurotransmitter Agents - physiology</subject><subject>Opioid Peptides - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Opioid, delta - analysis</subject><subject>Receptors, Opioid, delta - antagonists &amp; inhibitors</subject><subject>Receptors, Opioid, delta - physiology</subject><subject>Receptors, Opioid, kappa - analysis</subject><subject>Receptors, Opioid, kappa - antagonists &amp; inhibitors</subject><subject>Receptors, Opioid, kappa - physiology</subject><subject>Receptors, Opioid, mu - analysis</subject><subject>Receptors, Opioid, mu - physiology</subject><subject>Reflex - drug effects</subject><subject>Reflex - physiology</subject><subject>Rodents</subject><subject>Spinal cord</subject><subject>Spinal Cord - chemistry</subject><subject>Spinal Cord - physiology</subject><subject>Stomach - physiology</subject><subject>Sympathetic Nervous System - drug effects</subject><subject>Sympathetic Nervous System - physiology</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkVFv1SAUx4lxcdfpV1BiovGlV6AF2r2ZZdMlM77MZ0Ip3MsNLRWort9-1Nu4ZYnxiQR-538O5wfAW4y2GFPy6SDH0Y37OVrvtgjjEm0JQvQZ2ORXUmCG8HOwqTlFBac1PwUvYzwghKuK4hfgFDPCmgxuwPzNd5OTyfoBegOVDJ31v2RU-TJAfadsksmHGQYdRz9EHaEdYJApwnaGKcgho0kO2k8R9nI36GQVjMn2a-o5DN7pJTvtNYyjHaSDyofuFTgx0kX9ej3PwI-ry9uLr8XN9y_XF59vCkWrMhWkNEoqgzpFTU2l4ZQaybnEmnFZGtLollSaVqxtDCO8pZSUreaYKqUxyZs5Ax-OuWPwPycdk-htVNq549CCcVZVeVP_BTFHTVnXKIPvnoAHP4X8rygIIbipCVrS-BFSwccYtBFjsL0Ms8BILA7FY4fij0OxOMyVb9b4qe1191C3SsvA-xXInqQzWYKy8YHjDCFEeOY-Hrm93e1_26DF2s3v5qV7ngSJUjSEZbT6N3o1OXer79JS87dEjJ0p7wGljcy4</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Zhou (Yi Syuu), Wei</creator><creator>Hsiao, Ian</creator><creator>Lin, Vernon W. 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Unilateral magnetic stimulation (30% intensity, 2 Hz) at the Jianshi-Neiguan acupoints (pericardial meridian, P 5–6) overlying the median nerve on the forelimb for 24 min significantly decreased the reflex pressor response by 32%. This effect was noticeable by 20 min of magnetic stimulation and continued for 24 min. Median nerve denervation abolished the inhibitory effect of magnetic stimulation, indicating the importance of somatic afferent input. Unilateral EA (0.3–0.5 mA, 2 Hz) at P 5–6 using similar durations of stimulation similarly inhibited the response (35%). The inhibitory effects of EA occurred earlier and were marginally longer (20 min) than magnetic stimulation. Magnetic stimulation at Guangming-Xuanzhong acupoints (gallbladder meridian, GB 37–39) overlying the superficial peroneal nerve on the hindlimb did not attenuate the reflex. 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Syuu), Medical Science 1 C240, College of Medicine, Univ. of California, Irvine, CA 92697-4075 (e-mail: wzhou2{at}uci.edu )</abstract><cop>Bethesda, MD</cop><pub>Am Physiological Soc</pub><pmid>16269522</pmid><doi>10.1152/japplphysiol.01130.2005</doi><tpages>7</tpages></addata></record>
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subjects Afferent Pathways - physiology
Animals
Biological and medical sciences
Blood Pressure - physiology
Cardiovascular Physiological Phenomena
Cardiovascular system
Cardiovascular System - drug effects
Cardiovascular System - innervation
Electroacupuncture
Enkephalin, Leucine - analogs & derivatives
Enkephalin, Leucine - pharmacology
Fundamental and applied biological sciences. Psychology
Magnetics
Magnetism
Male
Median Nerve - physiology
Naloxone - pharmacology
Neurotransmitter Agents - physiology
Opioid Peptides - physiology
Rats
Rats, Sprague-Dawley
Receptors, Opioid, delta - analysis
Receptors, Opioid, delta - antagonists & inhibitors
Receptors, Opioid, delta - physiology
Receptors, Opioid, kappa - analysis
Receptors, Opioid, kappa - antagonists & inhibitors
Receptors, Opioid, kappa - physiology
Receptors, Opioid, mu - analysis
Receptors, Opioid, mu - physiology
Reflex - drug effects
Reflex - physiology
Rodents
Spinal cord
Spinal Cord - chemistry
Spinal Cord - physiology
Stomach - physiology
Sympathetic Nervous System - drug effects
Sympathetic Nervous System - physiology
title Modulation of cardiovascular excitatory responses in rats by transcutaneous magnetic stimulation: role of the spinal cord
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