Literature DB >> 17646572

Training-induced pressure fall in spontaneously hypertensive rats is associated with reduced angiotensinogen mRNA expression within the nucleus tractus solitarii.

Jorge Vinicius Cestari Felix1, Lisete Compagno Michelini.   

Abstract

Knowing that exercise training reduces arterial pressure in hypertensive individuals and that pressure fall is accompanied by blockade of brain renin-angiotensin system, we sought to investigate whether training (T) affects central renin-angiotensin system. Spontaneously hypertensive rats (SHRs) and normotensive Wistar-Kyoto controls (WKY) were submitted to training or kept sedentary (S) for 3 months. After functional recordings, brain was removed and processed for autoradiography (brain stem sequential slices hybridized with (35)S-oligodeoxynucleotide probes for angiotensinogen [Aogen] and angiotensin II type 1 [AT(1A)] receptors). Resting arterial pressure and heart rate were higher in SHR(S) (177+/-2 mm Hg, 357+/-12 bpm versus 121+/-1 mm Hg, 320+/-9 bpm in WKY(S); P<0.05). Training was equally effective to enhance treadmill performance and to cause resting bradycardia (-10%) in both groups. Training-induced blood pressure fall (-6.3%) was observed only in SHR(T). In SHR(S) (versus WKY(S)) AT(1A) and Aogen mRNA expression were significantly increased within the NTS and area postrema (average of +67% and +41% for AT(1A) and Aogen, respectively; P<0.05) but unchanged in the gracilis nucleus. Training did not change AT(1A) expression but reduced NTS and area postrema Aogen mRNA densities specifically in SHR(T) (P<0.05 versus SHR(S), with values within the range of WKY groups). In SHRs, NTS Aogen mRNA expression was correlated with resting pressure (y=5.95x +41; r=0.55; P<0.05), with no significant correlation in the WKY group. Concurrent training-induced reductions of both Aogen mRNA expression in brain stem cardiovascular-controlling areas and mean arterial pressure only in SHRs suggest that training is as efficient as the renin-angiotensin blockers to reduce brain renin-angiotensin system overactivity and to decrease arterial pressure.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17646572     DOI: 10.1161/HYPERTENSIONAHA.107.094474

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  14 in total

Review 1.  Regulation of sympathetic vasomotor activity by the hypothalamic paraventricular nucleus in normotensive and hypertensive states.

Authors:  Roger A Dampney; Lisete C Michelini; De-Pei Li; Hui-Lin Pan
Journal:  Am J Physiol Heart Circ Physiol       Date:  2018-08-10       Impact factor: 4.733

Review 2.  Central neural control of sympathetic nerve activity in heart failure following exercise training.

Authors:  Kaushik P Patel; Hong Zheng
Journal:  Am J Physiol Heart Circ Physiol       Date:  2011-11-18       Impact factor: 4.733

3.  Hypertension induces additional cardiometabolic impairments and attenuates aerobic exercise training adaptations in fructose-fed ovariectomized rats.

Authors:  Janaina de O Brito-Monzani; Iris Callado Sanches; Nathalia Bernardes; Kátia Ponciano; Ivana C Moraes-Silva; Maria-Cláudia Irigoyen; Susana Llesuy; Kátia De Angelis
Journal:  Hypertens Res       Date:  2017-11-02       Impact factor: 3.872

4.  Dynamic exercise training prevents exercise pressor reflex overactivity in spontaneously hypertensive rats.

Authors:  Masaki Mizuno; Gary A Iwamoto; Wanpen Vongpatanasin; Jere H Mitchell; Scott A Smith
Journal:  Am J Physiol Heart Circ Physiol       Date:  2015-07-10       Impact factor: 4.733

Review 5.  Effects of exercise training on chronic inflammation in obesity : current evidence and potential mechanisms.

Authors:  Tongjian You; Nicole C Arsenis; Beth L Disanzo; Michael J Lamonte
Journal:  Sports Med       Date:  2013-04       Impact factor: 11.136

6.  Intrathecal fentanyl abolishes the exaggerated blood pressure response to cycling in hypertensive men.

Authors:  Thales C Barbosa; Lauro C Vianna; Igor A Fernandes; Eliza Prodel; Helena N M Rocha; Vinicius P Garcia; Natalia G Rocha; Niels H Secher; Antonio C L Nobrega
Journal:  J Physiol       Date:  2016-01-15       Impact factor: 5.182

7.  Early Training-Induced Reduction of Angiotensinogen in Autonomic Areas-The Main Effect of Exercise on Brain Renin-Angiotensin System in Hypertensive Rats.

Authors:  Laiali Jurdi Chaar; Tatiana Pereira Alves; Alvaro Martins Batista Junior; Lisete Compagno Michelini
Journal:  PLoS One       Date:  2015-09-15       Impact factor: 3.240

8.  Time-dependent effects of training on cardiovascular control in spontaneously hypertensive rats: role for brain oxidative stress and inflammation and baroreflex sensitivity.

Authors:  Gustavo S Masson; Tassia S R Costa; Lidia Yshii; Denise C Fernandes; Pedro Paulo Silva Soares; Francisco R Laurindo; Cristoforo Scavone; Lisete C Michelini
Journal:  PLoS One       Date:  2014-05-01       Impact factor: 3.240

9.  Exercise training normalizes ACE and ACE2 in the brain of rabbits with pacing-induced heart failure.

Authors:  Sumit Kar; Lie Gao; Irving H Zucker
Journal:  J Appl Physiol (1985)       Date:  2010-01-21

10.  Assessment of maximal lactate steady state during treadmill exercise in SHR.

Authors:  Jeeser Alves Almeida; Bernardo de Assis Petriz; Clarissa Pedrosa da Costa Gomes; Rinaldo Wellerson Pereira; Octávio Luiz Franco
Journal:  BMC Res Notes       Date:  2012-11-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.