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Environmental Tobacco Smoke Exposure during Intrauterine Period, Promotes Caspase Dependent and Independent DNA Fragmentation in Sertoli-Germ Cells
Author(s) -
Beril Yüksel,
Sevtap Kılıç,
Neşe Lortlar,
Nicel Taşdemir,
S Sertyel,
Yeşim Bardakçı,
Tarık Aksu,
Sertaç Batıoğlu
Publication year - 2014
Publication title -
isrn obstetrics and gynecology
Language(s) - English
Resource type - Journals
eISSN - 2090-4444
pISSN - 2090-4436
DOI - 10.1155/2014/170124
Subject(s) - algorithm , dna fragmentation , apoptosis , medicine , chemistry , andrology , mathematics , programmed cell death , biochemistry
Objectives . To investigate the effect of cigarette smoke exposure during intrauterine period on neonatal rat testis. Methods . Twenty-five rats were randomized to be exposed to cigarette smoke with the Walton Smoking Machine or to room air during their pregnancies. The newborn male rats ( n = 21) were grouped as group 1 ( n = 15) which were exposed to cigarette smoke during intrauterine life and group 2 ( n = 6) which were exposed to room air during intrauterine life. The orchiectomy materials were analyzed with TUNEL immunofluorescent staining for detection of DNA damage. To detect apoptosis, immunohistochemical analyses with caspase-3 were performed. Primary outcomes were apoptotic index and immunohistochemical scores (HSCORES); secondary outcomes were Sertoli-cell count and birth-weight of rats. Results . Sertoli cell apoptosis was increased in group 1 (HSCORE = 210.6 ± 41.9) when compared to group 2 (HSCORE = 100.0 ± 17.8) ( P = 0.001). Sertoli cell count was decreased in group 1 ( P = 0.043). The HSCORE for the germ cells was calculated as 214.0 ± 46.2 in group 1 and 93.3 ± 10.3 in group 2 ( P = 0.001) referring to an increased germ cell apoptosis in group 1. The apoptotic indexes for group 1 were 49.6 ± 9.57 and 29.98 ± 2.34 for group 2 ( P = 0.001). The immunofluorescent technique demonstrated increased DNA damage in seminiferous epithelium in group 1. Conclusions . Intrauterine exposure to cigarette smoke adversely affects neonatal testicular structuring and diminishes testicular reserve.

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