HU is used in β-TI patients in order to KRX0401 decrease the need for transfusion and augment hematological response. Bradai et al.6 reported clinical

and hematologic improvement with HU and regression of extramedullary hematopoietic masses in patients with β-TI. The literature contains only a few studies on the side effects of HU in β-TI. Ali T. Taher7 showed that HU treatment is protective for extramedullary hematopoiesis, pulmonary hypertension, leg ulcers, and hypothyroidism. In our previous study on low-dose HU (mean 10.74 mg/kg/day), Inhibitors,research,lifescience,medical adverse effects were recorded in 44 (30.7%) patients. Dermatological side effects, followed by neurological and gastrointestinal adverse effects, were commonly seen without any reports of endocrine abnormality.9 We detected a frequency of 10 (9.4%) for hypothyroidism in all our studied β-TI patients. There was no correlation between HU consumption and Inhibitors,research,lifescience,medical hormonal disturbance in our patients. To the best of our knowledge, there is no report on the effect of HU on thyroid status in β-TI patients to compare with our result. Patients with β-TI should be meticulously followed up for the early detection and management of newly developed complications. Conclusion In our study, we found that HU at a dose

of 8–15 mg/kg/day has no significant association with thyroid function Inhibitors,research,lifescience,medical in β-TI patients and it could be used as a safe treatment in these patients. Given the Inhibitors,research,lifescience,medical rise in mean HbF levels following HU therapy and decrease in transfusion requirement and iron overload complications like thyroid dysfunction in thalassemia patients, HU therapy may be protective for hypothyroidism. It should be mentioned that our study was limited due to the small number of patients in each group, which shows the Inhibitors,research,lifescience,medical need for conducting further studies with higher numbers of patients to find more accurate statistical relationships. Acknowledgment The authors thank Shiraz University of Medical Sciences for its financial support. Many thanks are also due to Shirin

Parand at the Hematology Research Center, Shiraz University of Medical Sciences and Maryam Zekavat for editorial assistance (-)-p-Bromotetramisole Oxalate with the manuscript. This paper is part of the thesis of O. R. Zekavat (Project No. 2280). Conflict of interest: None declared.
Background: Nandrolone decanoate (ND) is an anabolic androgenic steroid (AAS) which influences the ovarian structure and function. We assessed the effects of ND on the ovarian volume, number of primordial follicles, and level of hormones and also evaluated the modulatory effects of gonadotropins on the histopathological changes imposed by the administration of ND. Methods: Six groups of Sprague-Dawley adult female rats (n=30) were used. The experimental rats were injected intraperitoneally with 3 and 10 mg/kg ND with or without human menopausal gonadotropin (hMG), 10 IU weekly for one month.