Exacerbated pressor and sympathoexcitatory effects of central Elabela in spontaneously hypertensive rats

Am J Physiol Heart Circ Physiol. 2020 Jan 1;318(1):H124-H134. doi: 10.1152/ajpheart.00449.2019. Epub 2019 Dec 13.

Abstract

Elabela (ELA) is a newly discovered peptide that acts as a novel endogenous ligand of angiotensin receptor-like 1 (APJ) receptor. This study was designed to evaluate the effects of ELA-21 in paraventricular nucleus (PVN) on blood pressure and sympathetic nerve activity in spontaneously hypertensive rats (SHR). Experiments were performed in male Wistar-Kyoto rats (WKY) and SHR. ELA expression was upregulated in PVN of SHR. PVN microinjection of ELA-21 increased renal sympathetic nerve activity (RSNA), mean arterial pressure (MAP), heart rate (HR), plasma norepinephrine, and arginine vasopressin (AVP) levels in SHR. Intravenous injection of ELA-21 significantly decreased MAP and HR in both WKY and SHR, but only induced a slight decrease in RSNA. APJ antagonist F13A in PVN abolished the effects of ELA-21 on RSNA, MAP and HR. Intravenous infusion of both ganglionic blocker hexamethonium and AVP V1a receptor antagonist SR49059 caused significant reduction in the effects of ELA-21 on RSNA, MAP and HR in SHR, while combined administration of hexamethonium and SR49059 abolished the effects of ELA-21. ELA-21 microinjection stimulated Akt and p85α subunit of phosphatidylinositol 3-kinase (PI3K) phosphorylation in PVN, whereas PI3K inhibitor LY294002 or Akt inhibitor MK-2206 almost abolished the effects of ELA-21 on RSNA, MAP, and HR. Chronic PVN infusion of ELA-21 induced sympathetic activation, hypertension, and AVP release accompanied with cardiovascular remodeling in normotensive WKY. In conclusion, ELA-21 in PVN induces exacerbated pressor and sympathoexcitatory effects in hypertensive rats via PI3K-Akt pathway.NEW & NOTEWORTHY We demonstrated that PVN microinjection of ELA-21 increases sympathetic nerve activity and blood pressure, which can be abolished by pretreatment of APJ antagonist. This is the first demonstration that central ELA can induce hypertension. The pressor effects in PVN are mediated by both sympathetic activation and vasopressin release via PI3K-Akt pathway. Our data confirm that ELA is upregulated in the PVN of SHR and so may be involved in the pressor and sympathoexcitatory effects in hypertension.

Keywords: Elabela; hypertension; paraventricular nucleus; sympathetic; vasopressin.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine Vasopressin / blood
  • Arterial Pressure / drug effects*
  • Class Ia Phosphatidylinositol 3-Kinase / metabolism
  • Disease Models, Animal
  • Heart Rate / drug effects
  • Hypertension / chemically induced*
  • Hypertension / genetics
  • Hypertension / metabolism
  • Hypertension / physiopathology
  • Injections, Intravenous
  • Male
  • Microinjections
  • Norepinephrine / blood
  • Paraventricular Hypothalamic Nucleus / drug effects*
  • Paraventricular Hypothalamic Nucleus / metabolism
  • Paraventricular Hypothalamic Nucleus / physiopathology
  • Peptide Hormones / administration & dosage*
  • Peptide Hormones / metabolism
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Signal Transduction
  • Sympathetic Nervous System / drug effects*
  • Sympathetic Nervous System / metabolism
  • Sympathetic Nervous System / physiopathology

Substances

  • LOC100912649 protein, rat
  • Peptide Hormones
  • Arginine Vasopressin
  • Class Ia Phosphatidylinositol 3-Kinase
  • Pik3r1 protein, mouse
  • Proto-Oncogene Proteins c-akt
  • Norepinephrine