Central administration of metformin into the third ventricle of C57BL/6 mice decreases meal size and number and activates hypothalamic S6 kinase
- Authors
- Kim, Hyun-Ju; Park, Eun-Young; Oh, Mi-Jeong; Park, Sung-Soo; Shin, Kyung-Ho; Choi, Sang-Hyun; Chun, Boe-Gwun; Kim, Dong-Hoon
- Issue Date
- 9월-2013
- Publisher
- AMER PHYSIOLOGICAL SOC
- Keywords
- metformin; energy homeostasis; hypothalamus; S6 kinase; AMP-activated protein kinase; meal pattern
- Citation
- AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, v.305, no.5, pp.R499 - R505
- Indexed
- SCIE
SCOPUS
- Journal Title
- AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
- Volume
- 305
- Number
- 5
- Start Page
- R499
- End Page
- R505
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/102206
- DOI
- 10.1152/ajpregu.00099.2013
- ISSN
- 0363-6119
- Abstract
- Administration of metformin is known to reduce both body weight and food intake. Although the hypothalamus is recognized as a critical regulator of energy balance and body weight, there is currently no evidence for an effect of metformin in the hypothalamus. Therefore, we sought to determine the central action of metformin on energy balance and body weight, as well as its potential involvement with key hypothalamic energy sensors, including adenosine monophosphate-activated protein kinase (AMPK) and S6 kinase (S6K). We used meal pattern analysis and a conditioned taste aversion (CTA) test and measured energy expenditure in C56BL/6 mice administered metformin (0, 7.5, 15, or 30 mu g) into the third ventricle (I3V). Furthermore, we I3V-administered either control or metformin (30 mu g) and compared the phosphorylation of AMPK and S6K in the mouse mediobasal hypothalamus. Compared with the control, I3V administration of metformin decreased body weight and food intake in a dose-dependent manner and did not result in CTA. Furthermore, the reduction in food intake induced by I3V administration of metformin was accomplished by decreases in both nocturnal meal size and number. Compared with the control, I3V administration of metformin significantly increased phosphorylation of S6K at Thr(389) and AMPK at Ser(485/491) in the mediobasal hypothalamus, while AMPK phosphorylation at Thr(172) was not significantly altered. Moreover, I3V rapamycin pretreatment restored the metformin-induced anorexia and weight loss. These results suggest that the reduction in food intake induced by the central administration of metformin in the mice may be mediated by activation of S6K pathway.
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Collections - College of Medicine > Department of Medical Science > 1. Journal Articles
- Graduate School > Department of Biomedical Sciences > 1. Journal Articles
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