Exercise training attenuates hypertension and cardiac hypertrophy by modulating neurotransmitters and cytokines in hypothalamic paraventricular nucleus

PLoS One. 2014 Jan 17;9(1):e85481. doi: 10.1371/journal.pone.0085481. eCollection 2014.

Abstract

Aims: Regular exercise as an effective non-pharmacological antihypertensive therapy is beneficial for prevention and control of hypertension, but the central mechanisms are unclear. In this study, we hypothesized that chronic exercise training (ExT) delays the progression of hypertension and attenuates cardiac hypertrophy by up-regulating anti-inflammatory cytokines, reducing pro-inflammatory cytokines (PICs) and restoring the neurotransmitters balance in the hypothalamic paraventricular nucleus (PVN) in young spontaneously hypertensive rats (SHR). In addition, we also investigated the involvement of nuclear factor-κB (NF-κB) p65 and NAD(P)H oxidase in exercise-induced effects.

Methods and results: Moderate-intensity ExT was administrated to young normotensive Wistar-Kyoto (WKY) and SHR rats for 16 weeks. SHR rats had a significant increase in mean arterial pressure and cardiac hypertrophy. SHR rats also had higher levels of glutamate, norepinephrine (NE), phosphorylated IKKβ, NF-κB p65 activity, NAD(P)H oxidase subunit gp91(phox), PICs and the monocyte chemokine protein-1 (MCP-1), and lower levels of gamma-aminobutyric acid (GABA) and interleukin-10 (IL-10) in the PVN. These SHR rats also exhibited higher renal sympathetic nerve activity (RSNA), and higher plasma levels of PICs, and lower plasma IL-10. However, ExT ameliorates all these changes in SHR rats.

Conclusion: These findings suggest that there are the imbalances between excitatory and inhibitory neurotransmitters and between pro- and anti-inflammatory cytokines in the PVN of SHR rats, which at least partly contributing to sympathoexcitation, hypertension and cardiac hypertrophy; chronic exercise training attenuates hypertension and cardiac hypertrophy by restoring the balances between excitatory and inhibitory neurotransmitters and between pro- and anti-inflammatory cytokines in the PVN; NF-κB and oxidative stress in the PVN may be involved in these exercise-induced effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arterial Pressure / physiology*
  • Cardiomegaly / metabolism
  • Cardiomegaly / physiopathology
  • Cardiomegaly / therapy*
  • Cytokines / metabolism*
  • Glutamic Acid / metabolism
  • Hypertension / metabolism
  • Hypertension / physiopathology
  • Hypertension / therapy*
  • Male
  • NADPH Oxidases / metabolism
  • NF-kappa B / metabolism
  • Norepinephrine / metabolism
  • Oxidative Stress / physiology
  • Paraventricular Hypothalamic Nucleus / metabolism*
  • Physical Conditioning, Animal / physiology*
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Sympathetic Nervous System / metabolism
  • Sympathetic Nervous System / physiopathology
  • gamma-Aminobutyric Acid / metabolism

Substances

  • Cytokines
  • NF-kappa B
  • Glutamic Acid
  • gamma-Aminobutyric Acid
  • NADPH Oxidases
  • Norepinephrine

Grants and funding

This study was supported by National Basic Research Program of China (No. 2012CB517805) and National Natural Science Foundation of China (Nos. 31271254, 81170248, 81070199, 31171095, 31171141). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.