Literature DB >> 9546615

Streptozotocin-induced diabetes increases (Ca2+-Mg2+)-ATPase activity in hepatic plasma membranes of rats: involvement of protein kinase C.

H Takahashi1, T Murata, Y Hanahisa, M Yamaguchi.   

Abstract

The alteration in calcium transport in the liver of rats with streptozocin(STZ)-diabetic state was investigated. STZ (6 mg/100 g body weight) was subcutaneously administered in rats, and 1 or 2 weeks later they were sacrificed by bleeding. STZ administration caused a remarkable elevation of serum glucose concentration. Liver calcium content was significantly increased by STZ administration. Hepatic plasma membrane (Ca2+-Mg2+)-ATPase activity was markedly elevated by STZ administration. This increase was completely abolished by the presence of staurosporine (10(-7)-10(-5) M), an inhibitor of protein kinase C, in the enzyme reaction mixture, suggesting an involvement of protein kinase C signalling. Moreover, the STZ-induced increase in liver plasma membrane (Ca2+-Mg2+)-ATPase activity was significantly raised by the presence of okadaic acid (10(-5) and 10(-4) M). Meanwhile, the STZ-increased (Ca2+-Mg2+)-ATPase activity was not appreciably altered by the presence of anti-regucalcin IgG in the reaction mixture, indicating that the activatory protein regucalcin does not participate in the elevation of the enzyme activity. The present study demonstrates that STZ-induced diabetes causes the increase in hepatic plasma membrane (Ca2+-Mg2+)-ATPase activity of rats.

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Year:  1998        PMID: 9546615     DOI: 10.1023/a:1006871615498

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  27 in total

1.  Oral administration of vanadate to streptozotocin-diabetic rats restores the glucose-induced activation of liver glycogen synthase.

Authors:  M Bollen; M Miralpeix; F Ventura; B Toth; R Bartrons; W Stalmans
Journal:  Biochem J       Date:  1990-04-01       Impact factor: 3.857

2.  Stimulatory effect of regucalcin on ATP-dependent calcium transport in rat liver plasma membranes.

Authors:  H Takahashi; M Yamaguchi
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

3.  Regulation of Ca2+-Mg2+-ATPase activity in hepatocyte plasma membranes by vasopressin and phenylephrine.

Authors:  S H Lin; M A Wallace; J N Fain
Journal:  Endocrinology       Date:  1983-12       Impact factor: 4.736

4.  A high affinity calcium-stimulated magnesium-dependent ATPase in rat liver plasma membranes. Dependence of an endogenous protein activator distinct from calmodulin.

Authors:  S Lotersztajn; J Hanoune; F Pecker
Journal:  J Biol Chem       Date:  1981-11-10       Impact factor: 5.157

5.  Hepatic calcium-binding protein regucalcin concentration is decreased by streptozotocin-diabetic state and ethanol ingestion in rats.

Authors:  M Isogai; H Kurota; M Yamaguchi
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

6.  Hormone-specific defect in insulin regulation of (Ca2+ + Mg2+)-adenosine triphosphatase activity in kidney membranes from streptozocin non-insulin-dependent diabetic rats.

Authors:  J Levy; D Rempinski; T H Kuo
Journal:  Metabolism       Date:  1994-05       Impact factor: 8.694

7.  Vasopressin-, angiotensin II-, and alpha 1-adrenergic-induced inhibition of Ca2+ transport by rat liver plasma membrane vesicles.

Authors:  V Prpić; K C Green; P F Blackmore; J H Exton
Journal:  J Biol Chem       Date:  1984-02-10       Impact factor: 5.157

8.  Fe2+ and other divalent metal ions uncouple Ca2+ transport from (Ca2+-Mg2+)-ATPase in rat liver plasma membranes.

Authors:  F Pecker; S Lotersztajn
Journal:  J Biol Chem       Date:  1985-01-25       Impact factor: 5.157

9.  Increase of (Ca(2+)-Mg2+)-ATPase activity in hepatic plasma membranes of rats administered orally calcium: the endogenous role of regucalcin.

Authors:  H Takahashi; M Yamaguchi
Journal:  Mol Cell Biochem       Date:  1995-03-09       Impact factor: 3.396

10.  Streptozotocin-induced diabetes elicits the phosphorylation of hepatocyte Gi2 alpha at the protein kinase C site but not at the protein kinase A-controlled site.

Authors:  N J Morris; M Bushfield; M D Houslay
Journal:  Biochem J       Date:  1996-04-15       Impact factor: 3.857

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