Chemerin as a Driver of Hypertension: A Consideration

Author:

Ferland David J1,Mullick Adam E2,Watts Stephanie W1ORCID

Affiliation:

1. Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, USA

2. Cardiovascular Antisense Drug Discovery, Ionis Pharmaceuticals, Carlsbad, California, USA

Abstract

Abstract The protein chemerin (tazarotene-induced gene, TIG2; RARRES2) is a relatively new adipokine. Many studies support that circulating chemerin levels associate strongly and positively with body mass index, visceral fat, and blood pressure. Here, we focus on the specific relationship of chemerin and blood pressure with the goal of understanding whether and how chemerin drives (pathological) changes in blood pressure such that it could be interfered with therapeutically. We dissect the biosynthesis of chemerin and how current antihypertensive medications change chemerin metabolism. This is followed with a review of what is known about where chemerin is synthesized in the body and what chemerin and its receptors can do to the physiological function of organs important to blood pressure determination (e.g., brain, heart, kidneys, blood vessels, adrenal, and sympathetic nervous system). We synthesize from the literature our best understanding of the mechanisms by which chemerin modifies blood pressure, with knowledge that plasma/serum levels of chemerin may be limited in their pathological relevance. This review reveals several gaps in our knowledge of chemerin biology that could be filled by the collective work of protein chemists, biologists, pharmacologists, and clinicians.

Funder

American Heart Association

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Internal Medicine

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