Hexarelin, a Growth Hormone Secretagogue, Improves Lipid Metabolic Aberrations in Nonobese Insulin-Resistant Male MKR Mice.
Mosa. Rasha R; Huang. Lili L; Wu. Yeda Y; Fung. Chungyan C; Mallawakankanamalage. Oshini O; LeRoith. Derek D; Chen. Chen C
Key Findings
- Hexarelin improved glucose tolerance and insulin sensitivity in insulin‑resistant mice.
- Plasma and liver triglyceride levels were significantly reduced after treatment.
- Body composition shifted: fat mass decreased while lean mass increased, despite higher food intake.
Practical Outcomes
- For biohackers, the study suggests hexarelin might be a promising tool to improve metabolic health and promote leanness, but human data are missing and dosing would need careful conversion from mouse studies. Until safety and efficacy are proven in people, it remains an experimental option to watch rather than a ready‑to‑use protocol.
Summary
In a mouse study, giving the peptide hexarelin twice a day for 12 days lowered blood sugar problems, cut down fat in the blood and liver, and changed body composition by reducing fat and increasing lean muscle, even though the mice ate more. These results hint that hexarelin could help with insulin resistance and unwanted fat, but the work was done in a specific mouse model, not people.
Abstract
Despite the occurrence of dyslipidemia and its contribution to the development of insulin resistance in obese subjects, a growing number of studies have described abnormal lipid profiles among leaner persons. For example, individuals with an abnormal paucity or distribution of fat (lipodystrophy) develop severe insulin resistance, dyslipidemia, and hepatic steatosis. Deranged adipocyte metabolism and differentiation contribute to ectopic fat deposition and consequent development of insulin resistance. Growth hormone (GH) therapy has been shown to correct body composition abnormalities in some lipodystrophy patients. However, little is known about the effects of GH-releasing peptides in this regard. Hexarelin, a GH secretagogue, has recently been shown to have beneficial effects on fat metabolism via the CD36 receptor. In this study, the effects of twice daily intraperitoneal injections of hexarelin (200 μg/kg body weight) were examined in nonobese insulin-resistant MKR mice and corresponding wild-type FVB mice for 12 days. Hexarelin treatment significantly improved glucose and insulin intolerance and decreased plasma and liver triglycerides in MKR mice. These beneficial metabolic effects could be due to the improved lipid metabolism and enhanced adipocyte differentiation of white adipose tissue with hexarelin treatment. Interestingly, although food intake of hexarelin-treated MKR mice was significantly increased, this did not change total body weight. Moreover, hexarelin treatment corrected the abnormal body composition of MKR mice, as demonstrated by a decrease in fat mass and an increase in lean mass. Our results suggest a possible application of hexarelin in treatment of lipid disorders associated with the metabolic syndrome.
Study Information
pubmed
2017
2017-10-01T00:00:00.000Z
10.1210/en.2017-00168
10
71