Related Experiment Video
Updated: Dec 20, 2025

Evaluation of Tumor-infiltrating Leukocyte Subsets in a Subcutaneous Tumor Model
Published on: April 13, 2015
Chemerin as a Driver of Hypertension: A Consideration
David J Ferland1, Adam E Mullick2, Stephanie W Watts1
1Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan, USA.
Insights
Chemerin, a protein linked to obesity, may influence blood pressure. Understanding chemerin
Area of Science:
- Endocrinology and Metabolism
- Cardiovascular Physiology
Background:
- Chemerin (tazarotene-induced gene, TIG2; RARRES2) is an adipokine associated with obesity and elevated blood pressure.
- Existing research indicates a positive correlation between circulating chemerin levels, body mass index, visceral fat, and blood pressure.
Purpose of the Study:
- To investigate the specific relationship between chemerin and blood pressure.
- To elucidate the mechanisms by which chemerin may pathologically alter blood pressure for potential therapeutic targeting.
- To review chemerin biosynthesis, metabolism influenced by antihypertensive drugs, and its physiological roles in blood pressure regulation.
Main Methods:
- Literature synthesis and review of existing studies on chemerin.
- Dissection of chemerin biosynthesis and its interaction with antihypertensive medications.
- Analysis of chemerin's physiological effects on organs critical for blood pressure regulation (brain, heart, kidneys, vasculature, adrenal glands, sympathetic nervous system).
Main Results:
- Chemerin's role in blood pressure regulation is complex, involving multiple organ systems.
- While plasma chemerin levels correlate with blood pressure, their direct pathological relevance may be limited.
- Antihypertensive medications can influence chemerin metabolism.
Conclusions:
- Further research is needed to fully understand the mechanisms linking chemerin to blood pressure.
- Identifying knowledge gaps in chemerin biology is crucial for future investigations.
- Interdisciplinary collaboration among protein chemists, biologists, pharmacologists, and clinicians is essential to advance this field.
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.
Related Concept Videos
Hormonal Regulation of Blood Pressure
Epinephrine and Norepinephrine
The adrenal medulla releases epinephrine and norepinephrine, catecholamines that enhance and extend the sympathetic or "fight or flight" physiological response. These hormones escalate heart rate and the force of contraction...
Hypertension II: Pathophysiology
Psychoneuroimmunology: Cardiovascular Disease
A key area of focus in PNI is the relationship between stress and coronary...
Antihypertensive Drugs: Angiotensin-Converting Enzyme Inhibitors
Antihypertensive Drugs: Action of β1 Blockers
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

