Fakoya Francis Adelade, Caxton-Martins Ezekiel Ademola
Department of Anatomy and Cell Biology, Faculty of Basic Medical Sciences, Obafemi Awolowo University, Ile-Ife, Nigeria.
Folia Morphol (Warsz). 2004 May;63(2):195-202.
This study presents the effects of prenatal ethanol exposure on the morphology of the seminiferous tubules of the testes in the adult male rat. Timed-pregnant adult female Wistar rats (average weight 200 g) were given daily intragastric intubation of 5.8 g/kg ethanol between gestation days 9 and 12. Pair-fed and ad lib-fed animals served as controls. The pups were weighed at birth and weaned at 30 days. At 42 days of age the male offspring (n = 10) from each group were anaesthetised and the testes removed and weighed. Another set of male rats from each group (n = 6), were anaesthetised, whole body perfused and the testes removed and processed for paraffin embedding. Sections were subjected to morphological analysis and morphometric measurements based on computerised techniques following haematoxylin and eosin, PAS and reticulin staining. The results demonstrated that prenatal ethanol exposure induced persistent growth retardation and a 66% reduction in testicular weight and severely altered the morphology of the seminiferous tubules of adult male rats, causing a reduction in the cross-sectional area of the tubules by 18%, germinal epithelium thickness by 21% (p < 0.001) and an inhibition of spermatogenesis. The study showed the absence of reticulin fibres in the peritubular tissue of seminiferous tubules of prenatal ethanol-exposed adult male rats. The results imply that damage following prenatal ethanol exposure occurs irreversibly in utero and persists into adulthood in the exposed animals, which may have implications for male fertility.
本研究呈现了产前乙醇暴露对成年雄性大鼠睾丸生精小管形态的影响。对处于孕期特定阶段的成年雌性Wistar大鼠(平均体重200克),在妊娠第9至12天每天进行5.8克/千克乙醇的胃内插管。成对喂养和自由采食的动物作为对照。幼崽在出生时称重,并在30天断奶。42日龄时,对每组的雄性后代(n = 10)进行麻醉,摘除睾丸并称重。每组另取一组雄性大鼠(n = 6),进行麻醉、全身灌注,然后摘除睾丸并进行石蜡包埋处理。切片在苏木精和伊红染色以及PAS和网状纤维染色后,基于计算机技术进行形态学分析和形态测量。结果表明,产前乙醇暴露导致持续生长迟缓,睾丸重量减少66%,并严重改变成年雄性大鼠生精小管的形态,使小管横截面积减少18%,生精上皮厚度减少21%(p < 0.001),并抑制精子发生。研究显示,产前乙醇暴露的成年雄性大鼠生精小管的管周组织中不存在网状纤维。结果表明,产前乙醇暴露造成的损伤在子宫内不可逆转地发生,并在暴露动物成年后持续存在,这可能对雄性生育能力产生影响。