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  2. Increased activity of the orexin system in the paraventricular nucleus contributes to salt-sensitive hypertension

Increased activity of the orexin system in the paraventricular nucleus contributes to salt-sensitive hypertension

  • Am J Physiol Heart Circ Physiol. 2017 Dec 1;313(6):H1075-H1086. doi: 10.1152/ajpheart.00822.2016.
Michael J Huber 1 Yuanyuan Fan 1 2 Enshe Jiang 1 3 Fengli Zhu 1 Robert A Larson 1 Jianqun Yan 2 Ningjun Li 4 Qing-Hui Chen 1 5 Zhiying Shan 6 5
Affiliations

Affiliations

  • 1 Department of Kinesiology and Integrative Physiology, Michigan Technological University, Houghton, Michigan.
  • 2 Department of Physiology and Pathophysiology, Xi'an Jiaotong University School of Medicine, Xi'an, Shaanxi, China.
  • 3 Institute for Nursing and Health Research, Henan University, Kaifeng, China.
  • 4 Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, Virginia; and.
  • 5 Biotech Research Center, Michigan Technological University, Houghton, Michigan.
  • 6 Department of Kinesiology and Integrative Physiology, Michigan Technological University, Houghton, Michigan; [email protected].
Abstract

The orexin system is involved in arginine vasopressin (AVP) regulation, and its overactivation has been implicated in hypertension. However, its role in salt-sensitive hypertension (SSHTN) is unknown. Here, we tested the hypothesis that hyperactivity of the orexin system in the paraventricular nucleus (PVN) contributes to SSHTN via enhancing AVP signaling. Eight-week-old male Dahl salt-sensitive (Dahl S) and age- and sex-matched Sprague-Dawley (SD) rats were placed on a high-salt (HS; 8% NaCl) or normal-salt (NS; 0.4% NaCl) diet for 4 wk. HS intake did not alter mean arterial pressure (MAP), PVN mRNA levels of orexin receptor 1 (OX1R), or OX2R but slightly increased PVN AVP mRNA expression in SD rats. HS diet induced significant increases in MAP and PVN mRNA levels of OX1R, OX2R, and AVP in Dahl S rats. Intracerebroventricular infusion of orexin A (0.2 nmol) dramatically increased AVP mRNA levels and immunoreactivity in the PVN of SD rats. Incubation of cultured hypothalamus neurons from newborn SD rats with orexin A increased AVP mRNA expression, which was attenuated by OX1R blockade. In addition, increased cerebrospinal fluid Na+ concentration through intracerebroventricular infusion of NaCl solution (4 µmol) increased PVN OX1R and AVP mRNA levels and immunoreactivity in SD rats. Furthermore, bilateral PVN microinjection of the OX1R antagonist SB-408124 resulted in a greater reduction in MAP in HS intake (-16 ± 5 mmHg) compared with NS-fed (-4 ± 4 mmHg) anesthetized Dahl S rats. These results suggest that elevated PVN OX1R activation may contribute to SSHTN by enhancing AVP signaling.NEW & NOTEWORTHY To our best knowledge, this study is the first to investigate the involvement of the orexin system in salt-sensitive hypertension. Our results suggest that the orexin system may contribute to the Dahl model of salt-sensitive hypertension by enhancing vasopressin signaling in the hypothalamic paraventricular nucleus.

Keywords

orexin; paraventricular nucleus; salt-sensitive hypertension; sympathetic nerve activity; vasopressin.

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