Insulin-like actions of vanadate are mediated in an insulin-receptor-independent manner via nonreceptor protein tyrosine kinases and protein phosphotyrosine phosphatases

被引:55
作者
Shechter, Y
Li, JP
Meyerovitch, J
Gefel, D
Bruck, R
Elberg, G
Miller, DS
Shisheva, A
机构
[1] CHAIM SHEBA MED CTR, DEPT PEDIAT, TEL AVIV, ISRAEL
[2] KAPLAN HOSP, DEPT INTERNAL MED B, IL-76100 REHOVOT, ISRAEL
[3] WOLFSON GOVT HOSP, DEPT GASTROENTEROL, IL-58100 HOLON, ISRAEL
[4] NIEHS, RES TRIANGLE PK, NC 27709 USA
关键词
vanadium salts; insulin action; cytosolic protein tyrosine kinase; protein phosphotyrosine phosphatase; molybdate-permolybdate; tungstate-pertungstate;
D O I
10.1007/BF01075917
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Most or all mammalian cells contain vanadium at a concentration of 0.1-1.0 mu M. The bulk of the vanadium in cells is probably in the reduced vanadyl (IV) form. Although this element is essential and should be present in the diet in minute quantities, no known physiological role for vanadium has been found thus far. In the years 1975-1980 the vanadate ion was shown to act as an efficient inhibitor of Na+,K+-ATPase and of other related phosphohydrolyzes as well. In 1980 it was observed that vanadate vanadyl, when added to intact rat adipocytes, mimics the biological actions of insulin in stimulating hexose uptake and glucose oxidation. This initiated a long, currently active, field of research among basic scientists and diabetologists. Several of the aspects studied are reviewed here.
引用
收藏
页码:39 / 47
页数:9
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