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Erika M. Plisetskaya Elena Fabbri Thomas W. Moon Joaquim Gutiérrez Celestina Ottolenghi 《Fish physiology and biochemistry》1993,11(1-6):401-409
The questions addressed in this study were: 1) whether insulin added to the incubation medium can down-regulate 125I insulin binding to isolated hepatocytes of Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss); 2) whether quantitative assessment of insulin processing can be made on isolated fish liver cells; 3) how ambient temperatures
can affect insulin binding, and down-regulation of insulin receptors.
After isolation and a short (up to 4h) “metabolic recovery period”, liver cells were used either directly in 125I insulin binding assay or first preincubated for 18h at 4°C or for 3h at 15°C, with or without mammalian or salmon insulin
in concentrations ranging from 1 to 1000 nM.
Preincubation at 15°C, decreased binding capacity (number of binding sites per liver cell) in all five independent hepatocyte
preparations treated with 1000 nM insulin and in four out of five preparations treated with 100 nM insulin. At 4°C insulin
binding sites were down-regulated in less than 50% of all hepatocyte preparations and only in the presence of 1000 nM insulin.
Differential quantitive assessment was made of a) intact free insulin; b) insulin degraded; c) intact insulin bound to the
cell membrane; d) internalized but degraded insulin, and e) intact insulin internalized by liver cells. Hepatocytes preincubated
with 100 – 1000 nM insulin at 15°C bound and internalized less 125I insulin.
We hypothesize that in vivo, at water temperatures of 15°C and higher, extreme physiological levels of plasma insulin may regulate the numbers of insulin
receptors in the salmonid liver. In contrast, in fish inhabiting cold waters the regulation of insulin receptors by circulating
plasma insulin seems to be of little physiological importance.
Presented in part at the Western Regional Conference on Comparative Endrocrinology, Tempe, Arizona, U.S.A., 1991 and at the
Meeting of Italian Society of Experimental Biology, Sorrento, Italy, 1991. Supported by grants from NSF of the USA#DCB 8915935
to E.M.P., NSERC of Canada OPGA 6944 to T.W.M., North Atlantic Treaty Organization (NATO) grant #0926/87 to C.O. and E.M.P.,
and CYCIT grant of Spain to J.G. 相似文献
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C. Ottolenghi A. C. Puviani M. E. Gavioli E. Fabbri L. Brighenti E. M. Plisetskaya 《Fish physiology and biochemistry》1989,6(6):387-394
Glycogenolytic effects of salmon and mammalian glucagons, salmon glucagon-like peptide (GLP) and epinephrine were studied on liver cells isolated from catfish (Ictalurus melas). In spring and summer, salmo-glucagon (3×10–10 to 3×10–8 M) was more effective than its mammalian counterpart in the stimulation of glucose release and cAMP synthesis in hepatocytes. GLP was less potent as compared to both glucagons. -amylase activity was not affected by the treatment with either glucagon-family peptides or epinephrine.The comparison of the glycogenolytic effects of salmon glucagon to those of epinephrine reveals a greater potency of the latter hormone in the stimulation of cAMP synthesis, glycogen-phosphorylase activity and glucose release. Glycogen content in the liver cells was equally depleted after treatment with both of the two hormones. 相似文献
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