Mohammad Abdul Awal

Mono-(2-ethylhexyl) Phthalate (MEHP) Induces Spermatogenic Cell Apoptosis in Guinea Pig Testes at Prepubertal Stage In Vitro

The effects of mono-(2-ethylhexyl) phthalate (MEHP), an active metabolite of di-(2-ethylhexyl) phthalate (DEHP), on prepubertal guinea pig testes in vitro were investigated. The testes of 35-day-old guinea pigs were surgically excised. They were seeded in a defined medium containing antibiotics and administered MEHP at concentrations of 1, 10, and 100 nmol/ml, respectively. The control groups were administered a similar volume of corn oil vehicle. The tissues were incubated for 3, 6, and 9 h. The specimens were collected at 3, 6, and 9 h after treatment. They were fixed in 4%paraformaldehyde or 5% glutaraldehyde. For quantitation of the apoptotic spermatogenic cells, the terminal dUTP nick end-labeling (TUNEL) staining was performed by light microscopy. Detachment and displacement of spermatogenic cells, thin seminiferous epithelia, and Sertoli cell vacuolization were observed. Maximal testicular damage was recognized at 100 nmol/ml 9 h after MEHP treatment. The percentage (%) of apoptotic spermatogenic cells significantly increased at 3, 6, and 9 h after treatment, compared to the control groups. Because the loss of spermatogenic cells by MEHP treatment varies among species, the present study, using guinea pigs, was designed and conducted to obtain further information.

Histomorphological and morphometric studies of the pancreatic islet cells of diabetic rats treated with aqueous extracts of Momordica charantia (karela) fruits

Abstract Objective To investigate the effect of aqueous extract of Momordica charantia (karela) (M. charantia) fruits on blood glucose level, pancreatic weight changes and histopathology of pancreatic changes in the streptozotocin (STZ) induced diabetic rats. Methods Thirty-six albino rats were used in the experiment; diabetes mellitus was induced in 30 adult albino rats, using intraperitoneal injection of 55 mg/kg STZ. Six non diabetic rats remained as control (T1). The diabetic rats were randomly assigned into five equal groups: diabetic control (T2) without any treatment, groups T3, T4, T5 and T6 were treated with aqueous extract of karela fruits daily at a doses of 250, 500 and 750 mg/kg and glibenclamide (5 mg/kg) up to 90 d, respectively. At Day 90, all rats were sacrificed, the pancreases of the rats were excised and processed. Results The results of this study indicate that aqueous extract of M. charantia fruits was able to reduce blood glucose level significantly compared with the diabetic control group (P Conclusions The present study suggests that oral feeding of M. charantia fruit juice has a significant anti-hyperglycemic effect and may have a role in the regeneration of the β cells in STZ diabetic rats.

Bisphenol A‐induced morphological alterations in Sertoli and spermatogenic cells of immature Shiba goats in vitro: An ultrastructural study

Background and aimsThere is no information currently available regarding the effects of bisphenol A (BPA) on testes in ruminants. Therefore, to establish and clarify the effects of BPA in ruminants, testicular tissue cultures were obtained from immature Shiba goats.MethodsThe testes of 2-month-old Shiba goats were cut into smaller pieces and seeded in medium. At 1, 3, 6 and 9 h after administration of various concentrations of BPA, the specimens underwent light and transmission electron microscopic observationsResultsAt 1 h after BPA treatment, vacuolization and nuclear membrane rupture appeared within the nudeoplasm and cytoplasm of Sertoli cells. Such alterations tended to gradually increase in number in time- and dose-dependent manners. Thus, because of BPA treatment, apoptotic spermatogenic cells, necrotic spermatogenic cells, apoptotic Sertoli cells and necrotic Sertoli cells could be identified. Particularly in the Sertoli cell, ruptured vesicles could be found within the multivesicular nuclear body.ConclusionThe treatment with BPA at a low concentration tends to lead spermatogenic and Sertoli cells to apoptosis, whereas a higher concentration tends to lead spermatogenic and Sertoli cells to necrosis. Therefore, this study showed that testicular tissue culture is an advantageous avenue for screening the testicular toxicity of chemicals in ruminants.