(d)-β-Hydroxybutyrate Inhibits Adipocyte Lipolysis via the Nicotinic Acid Receptor PUMA-G
Merck & Co., Inc., Rahway, NJ, USA (United States) · Heidelberg University · +1 more institution
Abstract
As a treatment for dyslipidemia, oral doses of 1–3 grams of nicotinic acid per day lower serum triglycerides, raise high density lipoprotein cholesterol, and reduce mortality from coronary heart disease (Tavintharan, S., and Kashyap, M. L. (2001) Curr. Atheroscler. Rep. 3, 74–82). These benefits likely result from the ability of nicotinic acid to inhibit lipolysis in adipocytes and thereby reduce serum non-esterified fatty acid levels (Carlson, L. A. (1963) Acta Med. Scand. 173, 719–722). In mice, nicotinic acid inhibits lipolysis via PUMA-G, a Gi/o-coupled seven-transmembrane receptor expressed in adipocytes and activated macrophages (Tunaru, S., Kero, J., Schaub, A., Wufka, C., Blaukat, A., Pfeffer, K., and…
Citation impact
- FWCI
- 8.92
- Percentile
- 100%
- References
- 23
Authors
18- AKAndrew K.P. TaggartCorresponding
Merck & Co., Inc., Rahway, NJ, USA (United States)
- JKJukka Kero
Heidelberg University
- XGXiaodong Gan
Merck & Co., Inc., Rahway, NJ, USA (United States)
- TCTian‐Quan Cai
Merck & Co., Inc., Rahway, NJ, USA (United States)
- KCKang Cheng
Merck & Co., Inc., Rahway, NJ, USA (United States)
Topics & keywords
- Lipolysis
- Puma
- Adipocyte
- Chemistry
- Nicotinic agonist
- Receptor
- Biochemistry
- Adipose tissue
- Good health and well-being