Hepatocyte growth factor inhibits insulin-stimulated glycogen synthesis in primary cultured hepatocytes. 2003

Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
First Department of Surgery, Kansai Medical University, 10-15 Fumizonocho, Moriguchi, Osaka 570-8506, Japan.

OBJECTIVE Hepatocyte growth factor (HGF) plays an important role as a mitogen in liver regeneration. However, little is known about the metabolic effects of HGF in the liver. Studies were performed to examine whether HGF influences carbohydrate metabolism, which is drastically changed in the early course of the regeneration. METHODS Primary cultured rat hepatocytes were treated with glucoregulatory hormones such as insulin, glucagon and adrenaline in the presence or absence of HGF. Cellular glycogen deposition and activities of its metabolic enzymes were compared. RESULTS HGF inhibited insulin-stimulated glycogen deposition, but had no effect on glycogen degradation stimulated by glucagon and adrenaline. HGF decreased glycogen synthase activity and increased glycogen phosphorylase activity in insulin-stimulated hepatocytes, resulting in the inhibition of glycogen synthesis. Experiments with immunoprecipitation revealed that HGF had no effect on the upstream of insulin signaling including an activation of its receptor and association of insulin receptor substrate with phosphatidylinositol 3-kinase, indicating that HGF presumably affects further downstream of these events. CONCLUSIONS These results demonstrate that HGF interacts with insulin on glucose metabolism in hepatocytes. HGF may be involved in glucose regulation, and contribute to cell growth and maturation in addition to its mitogenic action during liver regeneration.

UI MeSH Term Description Entries
D007004 Hypoglycemic Agents Substances which lower blood glucose levels. Antidiabetic,Antidiabetic Agent,Antidiabetic Drug,Antidiabetics,Antihyperglycemic,Antihyperglycemic Agent,Hypoglycemic,Hypoglycemic Agent,Hypoglycemic Drug,Antidiabetic Agents,Antidiabetic Drugs,Antihyperglycemic Agents,Antihyperglycemics,Hypoglycemic Drugs,Hypoglycemic Effect,Hypoglycemic Effects,Hypoglycemics,Agent, Antidiabetic,Agent, Antihyperglycemic,Agent, Hypoglycemic,Agents, Antidiabetic,Agents, Antihyperglycemic,Agents, Hypoglycemic,Drug, Antidiabetic,Drug, Hypoglycemic,Drugs, Antidiabetic,Drugs, Hypoglycemic,Effect, Hypoglycemic,Effects, Hypoglycemic
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D008297 Male Males
D002455 Cell Division The fission of a CELL. It includes CYTOKINESIS, when the CYTOPLASM of a cell is divided, and CELL NUCLEUS DIVISION. M Phase,Cell Division Phase,Cell Divisions,Division Phase, Cell,Division, Cell,Divisions, Cell,M Phases,Phase, Cell Division,Phase, M,Phases, M
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D004347 Drug Interactions The action of a drug that may affect the activity, metabolism, or toxicity of another drug. Drug Interaction,Interaction, Drug,Interactions, Drug
D006003 Glycogen
D006006 Glycogen Synthase An enzyme that catalyzes the transfer of D-glucose from UDPglucose into 1,4-alpha-D-glucosyl chains. EC 2.4.1.11. Glycogen (Starch) Synthase,Glycogen Synthetase,Glycogen Synthase I,Synthase D,Synthase I,UDP-Glucose Glycogen Glucosyl Transferase,Synthase, Glycogen,Synthetase, Glycogen,UDP Glucose Glycogen Glucosyl Transferase
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D017208 Rats, Wistar A strain of albino rat developed at the Wistar Institute that has spread widely at other institutions. This has markedly diluted the original strain. Wistar Rat,Rat, Wistar,Wistar Rats

Related Publications

Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
May 1994, Regulatory peptides,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
January 1987, The Journal of biological chemistry,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
March 1992, Biochemical and biophysical research communications,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
December 1982, Journal of cellular physiology,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
May 2003, Diabetes, obesity & metabolism,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
December 1985, The Journal of antibiotics,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
May 2002, The Journal of biological chemistry,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
January 1992, American journal of surgery,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
February 1996, Experimental cell research,
Masaki Kaibori, and A-Hon Kwon, and Shigeru Teshima, and Hideki Nakanishi, and Takahiro Kitano, and Yasuo Kamiyama, and Tadayoshi Okumura
March 1996, Endocrinology,
Copied contents to your clipboard!