Regularly swimming exercise modifies opioidergic neuromodulation in rostral ventrolateral medulla in hypertensive rats.


Journal

Brain research
ISSN: 1872-6240
Titre abrégé: Brain Res
Pays: Netherlands
ID NLM: 0045503

Informations de publication

Date de publication:
01 01 2022
Historique:
received: 04 07 2021
revised: 14 10 2021
accepted: 09 11 2021
pubmed: 18 11 2021
medline: 29 3 2022
entrez: 17 11 2021
Statut: ppublish

Résumé

Moderate exercise reduces arterial pressure (AP) and heart rate (HR) in spontaneously hypertensive rats (SHR) and changes neurotransmission in medullary areas involved in cardiovascular regulation. We investigated if regularly swimming exercise (SW) affects the cardiovascular adjustments mediated by opioidergic neuromodulation in the RVLM in SHR and Wistar-Kyoto (WKY) rats. Rats were submitted to 6 wks of SW. The day after the last exercise bout, α-chloralose-anesthetized rats underwent a cannulation of the femoral artery for AP and HR recordings, and Doppler flow probes were placed around the lower abdominal aorta and superior mesenteric artery. Bilateral injection of endomorphin-2 (EM-2, 0.4 mmol/L, 60 nL) into the RVLM increased MAP in SW-SHR (20 ± 4 mmHg, N = 6), which was lower than in sedentary (SED)-SHR (35 ± 4 mmHg, N = 6). The increase in MAP in SW-SHR induced by EM-2 into the RVLM was similar in SED- and SW-WKY. Naloxone (0.5 mmol/L, 60 nL) injected into the RVLM evoked an enhanced hypotension in SW-SHR (-66 ± 8 mmHg, N = 6) compared to SED-SHR (-25 ± 3 mmHg, N = 6), which was similar in SED- and SW-WKY. No significant changes were observed in HR after EM-2 or naloxone injections into the RVLM. Changes in hindquarter and mesenteric conductances evoked by EM-2 or naloxone injections into the RVLM in SW- or SED-SHR were not different. Mu Opioid Receptor expression by Western blotting was reduced in SW-SHR than in SED-SHR and SW-WKY. Therefore, regularly SW alters the opioidergic neuromodulation in the RVLM in SHR and modifies the mu opioid receptor expression in this medullary area.

Identifiants

pubmed: 34785257
pii: S0006-8993(21)00583-7
doi: 10.1016/j.brainres.2021.147726
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Narcotic Antagonists 0
Oligopeptides 0
Receptors, Opioid, mu 0
Naloxone 36B82AMQ7N
endomorphin 2 3PH5M0466G

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

147726

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Roberto L Almeida (RL)

Dept. Morphology and Physiology, Faculdade de Medicina do ABC, Centro Universitário FMABC, Santo Andre, SP, Brazil.

Cristiana A Ogihara (CA)

Dept. Morphology and Physiology, Faculdade de Medicina do ABC, Centro Universitário FMABC, Santo Andre, SP, Brazil.

Janaína S de Souza (JS)

Dept. Medicine, Federal University of Sao Paulo, Sao Paulo, SP, Brazil.

Kelen C Oliveira (KC)

Dept. Medicine, Federal University of Sao Paulo, Sao Paulo, SP, Brazil.

Eduardo M Cafarchio (EM)

Dept. Morphology and Physiology, Faculdade de Medicina do ABC, Centro Universitário FMABC, Santo Andre, SP, Brazil. Electronic address: eduardo.cafarchio@fmabc.net.

Larissa Tescaro (L)

Dept. Morphology and Physiology, Faculdade de Medicina do ABC, Centro Universitário FMABC, Santo Andre, SP, Brazil.

Rui M B Maciel (RMB)

Dept. Medicine, Federal University of Sao Paulo, Sao Paulo, SP, Brazil.

Gisele Giannocco (G)

Dept. Medicine, Federal University of Sao Paulo, Sao Paulo, SP, Brazil.

Monica A Sato (MA)

Dept. Morphology and Physiology, Faculdade de Medicina do ABC, Centro Universitário FMABC, Santo Andre, SP, Brazil.

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Classifications MeSH