Literature DB >> 3742704

An in vitro screening system for the nephrotoxicity of various platinum coordination complexes. A cytochemical study.

M A Batzer, S K Aggarwal.   

Abstract

Isolated rat kidney tubules were cultured in Earle's medium with and without the platinum coordination complexes. Aliquots were taken at 0, 1, 2, 3, 4, 5, 6, and 8 h and analyzed for the amount of Na+/K+-ATPase, Ca2+-ATPase, alkaline phosphatase, and acid phosphatase. Culture medium was also analyzed biochemically for the amounts of alkaline phosphatase present. There is a decrease in the various enzymes levels of the tubules after incubation in nephrotoxic analogues with a corresponding increase in the culture medium. These results compare favorably with in vivo studies. The alkaline phosphatase monitored in the rat kidney cross sections from both the normal and the drug-treated animals at 0, 3, 5, 10, and 20 days showed a correlation in the decrease of enzyme levels in the kidney with a corresponding increase in the urinary levels in both the Wistar and the Long Evans rats. The baseline levels were higher in the Long Evans rats than in the Wistar rats. After cisplatin (nephrotoxic) treatment the Long Evans rats had twice as much alkaline phosphatase in the urine at day 5 as the Wistar rats. Rats treated with cyclobutanedicarboxylatoplatinum (II) did have some alkaline phosphatase output in the urine in excess of the normal levels, but this increase was not so highly significant as to justify classifying the drug as nephrotoxic.

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Year:  1986        PMID: 3742704     DOI: 10.1007/bf00256686

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  19 in total

1.  Histochemical demonstration of protein-bound sulfhydryl groups.

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3.  Staining by neutral red and trypan blue in sequence for assaying vital and nonvital cultured cells.

Authors:  F A DeRenzis; A Schechtman
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4.  The cytochemical application of new potent inhibitors of alkaline phosphatases.

Authors:  M Borgers
Journal:  J Histochem Cytochem       Date:  1973-09       Impact factor: 2.479

Review 5.  Review of the current clinical status of platinum coordination complexes in cancer chemotherapy.

Authors:  J A Gottlieb; B Drewinko
Journal:  Cancer Chemother Rep       Date:  1975 May-Jun

Review 6.  Transport adenosine triphosphatases: properties and functions.

Authors:  F Schuurmans Stekhoven; S L Bonting
Journal:  Physiol Rev       Date:  1981-01       Impact factor: 37.312

7.  Quantification of nephrotoxicity in rabbits by automated morphometry of alkaline phosphatase stained kidney sections.

Authors:  E D Wachsmuth
Journal:  Histochemistry       Date:  1981

8.  A direct lead method for the electron microscopic visualization of alkaline phosphatase activity.

Authors:  J Hugon; M Borgers
Journal:  J Histochem Cytochem       Date:  1966-05       Impact factor: 2.479

Review 9.  Minireview. The nephrotoxicity of cisplatin.

Authors:  R S Goldstein; G H Mayor
Journal:  Life Sci       Date:  1983-02-14       Impact factor: 5.037

10.  Quercetin: a novel inhibitor of Ca2+ influx and exocytosis in rat peritoneal mast cells.

Authors:  C M Fewtrell; B D Gomperts
Journal:  Biochim Biophys Acta       Date:  1977-08-15
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  2 in total

1.  Platinum complex-induced dysfunction of cultured renal proximal tubule cells. A comparative study of carboplatin and transplatin with cisplatin.

Authors:  F Courjault; D Leroy; L Coquery; H Toutain
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

2.  The influence of very low doses of Cisplatin on tumor cell proliferation in vitro and on some hematological and enzymatic parameters of healthy rats.

Authors:  Elzbieta Malarczyk; Martyna Kandefer-Szerszeń; Anna Jarosz-Wilkołazka
Journal:  Nonlinearity Biol Toxicol Med       Date:  2003-01
  2 in total

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