Hormone-sensitive lipase deficiency suppresses insulin secretion from pancreatic islets of Lepob/ob mice
Creators
- Sekiya, Motohiro1
- Yahagi, Naoya2, 1
- Tamura, Yoshiaki1
- Okazaki, Hiroaki1
- Igarashi, Masaki1
- Ohta, Keisuke1
- Takanashi, Mikio1
- Kumagai, Masayoshi1
- Takase, Satoru1
- Nishi, Makiko1
- Takeuchi, Yoshinori1
- Izumida, Yoshihiko1
- Kubota, Midori1
- Ohashi, Ken1
- Iizuka, Yoko1
- Yagyu, Hiroaki3
- Gotoda, Takanari4
- Nagai, Ryozo5
- Shimano, Hitoshi6
- Yamada, Nobuhiro6
- and others
- 1. Department of Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655 (Japan)
- 2. Laboratory of Molecular Physiology on Energy Metabolism, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655 (Japan)
- 3. Division of Endocrinology and Metabolism, Department of Medicine, Jichi Medical University, Tochigi 329-0498 (Japan)
- 4. Department of Nephrology and Endocrinology, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655 (Japan)
- 5. Department of Cardiovascular Medicine, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655 (Japan)
- 6. Advanced Biomedical Applications, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Ibaragi 305-8575 (Japan)
Description
It has long been a matter of debate whether the hormone-sensitive lipase (HSL)-mediated lipolysis in pancreatic β-cells can affect insulin secretion through the alteration of lipotoxicity. We generated mice lacking both leptin and HSL (Lepob/ob/HSL-/-) and explored the role of HSL in pancreatic β-cells in the setting of obesity. Lepob/ob/HSL-/- developed elevated blood glucose levels and reduced plasma insulin levels compared with Lepob/ob/HSL+/+ in a fed state, while the deficiency of HSL did not affect glucose homeostasis in Lep+/+ background. The deficiency of HSL exacerbated the accumulation of triglycerides in Lepob/ob islets, leading to reduced glucose-stimulated insulin secretion. The deficiency of HSL also diminished the islet mass in Lepob/ob mice due to decreased cell proliferation. In conclusion, HSL affects insulin secretary capacity especially in the setting of obesity.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.bbrc.2009.07.078Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2009.07.078;
- PII
- S0006-291X(09)01400-4;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 387
- Journal Issue
- 3
- Journal Page Range
- p. 511-515
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45020630
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- BLOOD; CELL PROLIFERATION; GLUCOSE; HOMEOSTASIS; INSULIN; LEPTIN; LIPASES; METABOLIC DISEASES; MICE; PANCREAS; SECRETION; TRIGLYCERIDES
- Descriptors DEC
- ALDEHYDES; ANIMALS; BIOLOGICAL MATERIALS; BODY; BODY FLUIDS; CARBOHYDRATES; CARBOXYLESTERASES; DIGESTIVE SYSTEM; DISEASES; ENDOCRINE GLANDS; ENZYMES; ESTERASES; ESTERS; GLANDS; HEXOSES; HORMONES; HYDROLASES; LIPIDS; MAMMALS; MATERIALS; MONOSACCHARIDES; ORGANIC COMPOUNDS; ORGANS; PEPTIDE HORMONES; PEPTIDES; POLYPEPTIDES; PROTEINS; RODENTS; SACCHARIDES; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.