Research Repository

Leptin action in the dorsomedial hypothalamus increases sympathetic tone to brown adipose tissue in spite of systemic leptin resistance

Enriori, Pablo J and Sinnayah, Puspha and Simonds, Stephanie E and Rudaz, Cecilia Garcia and Cowley, Michael A (2011) Leptin action in the dorsomedial hypothalamus increases sympathetic tone to brown adipose tissue in spite of systemic leptin resistance. Journal of Neuroscience, 31 (34). pp. 12189-12197. ISSN 0270-6474

Full text for this resource is not available from the Research Repository.

Abstract

Leptin regulates body weight in mice by decreasing appetite and increasing sympathetic nerve activity (SNA), which increases energy expenditure in interscapular brown adipose tissue (iBAT). Diet-induced obese mice (DIO) are resistant to the anorectic actions of leptin. We evaluated whether leptin still stimulated sympathetic outflow in DIO mice. We measured iBAT temperature as a marker of SNA. We found that obese hyperleptinemic mice have higher iBAT temperature than mice on regular diet. Conversely, obese leptin-deficient ob/ob mice have lower iBAT temperature. Additionally, leptin increased SNA in obese (DIO and ob/ob) and control mice, despite DIO mice being resistant to anorectic action of leptin. We demonstrated that neurons in the dorsomedial hypothalamus (DMH) of DIO mice mediate the thermogenic responses to hyperleptinemia in obese mammals because blockade of leptin receptors in the DMH prevented the thermogenic effects of leptin. Peripheral Melotan II (MTII) injection increased iBAT temperature, but it was blunted by blockade of DMH melanocortin receptors (MC4Rs) by injecting agouti-related peptide (AgRP) directly into the DMH, suggesting a physiological role of the DMH on temperature regulation in animals with normal body weight. Nevertheless, obese mice without a functional melanocortin system (MC4R KO mice) have an increased sympathetic outflow to iBAT compared with their littermates, suggesting that higher leptin levels drive sympathoexcitation to iBAT by a melanocortin-independent pathway. Because the sympathetic nervous system contributes in regulating blood pressure, heart rate, and hepatic glucose production, selective leptin resistance may be a crucial mechanism linking adiposity and metabolic syndrome.

Item Type: Article
Uncontrolled Keywords: ResPubID24931, energy homeostasis, central leptin receptors, LRb, sympathetic nervous system, SNS, energy expenditure, brown adipose tissue, BAT, mitochondrial uncoupling protein 1, UCP-1
Subjects: Faculty/School/Research Centre/Department > School of Biomedical and Health Sciences
FOR Classification > 1101 Medical Biochemistry and Metabolomics
Depositing User: VUIR
Date Deposited: 28 Nov 2012 03:42
Last Modified: 28 Nov 2012 03:42
URI: http://vuir.vu.edu.au/id/eprint/10398
DOI: 10.1523/JNEUROSCI.2336-11.2011
ePrint Statistics: View download statistics for this item
Citations in Scopus: 35 - View on Scopus

Repository staff only

View Item View Item

Search Google Scholar