Literature DB >> 2711396

Characterization of cis-platinum-induced Sertoli cell dysfunction in rodents.

L M Pogach1, Y Lee, S Gould, W Giglio, M Meyenhofer, H F Huang.   

Abstract

The present study examined the effects of dosage and frequency of cis-platinum administration on various aspects of Sertoli cell function and its correlation with the status of spermatogenesis in rats 1 and 9 weeks after the initial drug administration. Adult male Sprague-Dawley rats were administered cis-platinum (10 mg/kg) intraperitoneally as a single dose or as five daily doses of 2 mg/kg. Electron microscopic observation of testicular tissues fixed in the presence of lanthanum revealed that cis-platinum administration resulted in leakage of the Sertoli cell tight junctions. This occurred as early as 24 hr after the five daily injections, and persisted at least 40 days. Testicular androgen-binding protein (ABP) content was not significantly affected by either treatment regimen after 1 or 9 weeks of recovery. On the other hand, serum ABP values were significantly elevated after 9 weeks of recovery. In addition, the increased sodium and decreased potassium concentrations in seminiferous tubular fluid noted in cis-platinum-treated animals were also indicative of abnormal Sertoli cell secretory function. Degeneration of spermatogenic cells was noted as early as 5 days after the last drug administration; and partial restoration of spermatogenesis was noted after 40 days of recovery. We conclude that in rats both morphological and biochemical properties of Sertoli cells are affected by cis-platinum administration. These changes in Sertoli cell function may be responsible for the cis-platinum-induced impairment of spermatogenesis in these animals.

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Year:  1989        PMID: 2711396     DOI: 10.1016/0041-008x(89)90239-1

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  7 in total

1.  Ghrelin partially protects against cisplatin-induced male murine gonadal toxicity in a GHSR-1a-dependent manner.

Authors:  Shannon D Whirledge; Jose M Garcia; Roy G Smith; Dolores J Lamb
Journal:  Biol Reprod       Date:  2015-01-28       Impact factor: 4.285

2.  Zinc acetate pretreatment ameliorates cisplatin-induced Sertoli cell dysfunction in Sprague-Dawley rats.

Authors:  L M Pogach; Y Lee; W Giglio; M Naumoff; H F Huang
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

3.  Effects of carboplatin on the testis. A histological study.

Authors:  P Köpf-Maier
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

4.  Sertoli cell function in albino rats treated with etoposide during prepubertal phase.

Authors:  Taiza Stumpp; Edna Freymüller; Sandra Maria Miraglia
Journal:  Histochem Cell Biol       Date:  2006-03-21       Impact factor: 2.531

Review 5.  Cell-Cell Interaction-Mediated Signaling in the Testis Induces Reproductive Dysfunction-Lesson from the Toxicant/Pharmaceutical Models.

Authors:  Lingling Wang; Tiao Bu; Xiaolong Wu; Sheng Gao; Xinyao Li; Angela Bryanne De Jesus; Chris K C Wong; Hao Chen; Nancy P Y Chung; Fei Sun; C Yan Cheng
Journal:  Cells       Date:  2022-02-09       Impact factor: 6.600

6.  The effect of mirtazapine on cisplatin-induced oxidative damage and infertility in rat ovaries.

Authors:  Durdu Altuner; Mine Gulaboglu; Omer Erkan Yapca; Nihal Cetin
Journal:  ScientificWorldJournal       Date:  2013-04-22

7.  Candesartan Mediated Amelioration of Cisplatin-Induced Testicular Damage Is Associated with Alterations in Expression Patterns of Nephrin and Podocin.

Authors:  Noritoshi Enatsu; Hideaki Miyake; Koji Chiba; Masato Fujisawa
Journal:  Biomed Res Int       Date:  2015-10-11       Impact factor: 3.411

  7 in total

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