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Hypothalamic-pituitary axis regulates hydrogen sulfide production SCIE SCOPUS

Title
Hypothalamic-pituitary axis regulates hydrogen sulfide production
Authors
SINGHA, SUBHANKARHINE, CHRISTOPHERKIM, HYO-JEONGZHU, YANHARPUTLUGIL, EYLULLONGCHAMP, ALBANMATOS, MARINA SOUZARAMADOSS, PREETIBAUERLE, KEVINBRACE, LEARASARA, JOHN M.OZAKI, C. KEITHCHENG, SHEUE-YANNAHN, KYO HANKIMMELMAN, ALECFISHER, FFOLLIOTT M.PISSIOS, PAVLOSWITHERS, DOMINIC J.SELMAN, COLINWANG, RUIYEN, KELVINLONGO, VALTER D.COHEN, PINCHASBARTKE, ANDRZEJKOPCHICK, JOHN J.MILLER, RICHARDHOLLENBERG, ANTHONY N.MITCHELL, JAMES R.
Date Issued
2017-06
Publisher
CELL PRESS
Abstract
Decreased growth hormone (GH) and thyroid hormone (TH) signaling are associated with longevity and metabolic fitness. The mechanisms underlying these benefits are poorly understood, but may overlap with those of dietary restriction (DR), which imparts similar benefits. Recently we discovered that hydrogen sulfide (H2S) is increased upon DR and plays an essential role in mediating DR benefits across evolutionary boundaries. Here we found increased hepatic H2S production in long-lived mouse strains of reduced GH and/or TH action, and in a cell-autonomous manner upon serum withdrawal in vitro. Negative regulation of hepatic H2S production by GH and TH was additive and occurred via distinct mechanisms, namely direct transcriptional repression of the H2S-producing enzyme cystathionine g-lyase (CGL) by TH, and substrate-level control of H2S production by GH. Mice lacking CGL failed to downregulate systemic T4 metabolism and circulating IGF-1, revealing an essential role for H2S in the regulation of key longevity-associated hormones.
URI
https://oasis.postech.ac.kr/handle/2014.oak/41232
DOI
10.1016/j.cmet.2017.05.003
ISSN
1550-4131
Article Type
Article
Citation
Cell Metabolism, vol. 25, no. 6, page. 1320 - 1333, 2017-06
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안교한AHN, KYO HAN
Dept of Chemistry
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