Diabetes mellitus and obesity are a growing overall medical issues, particularly in developed nations. Vitamin D deficiency is pandemic that has been involved in a different kind of disease. This study was intended to detect the effect of vitamin D deficiency and vitamin D receptor polymorphisms on type 2 diabetes mellitus (T2DM) patients through induction of obesity. 80 Egyptians T2DM patients and 20 non diabetic subjects were included in our research. Diabetic cases were categorized into two subgroups according to diabetic complications. PCR-RFLP for vit D receptor polymorphisms and vit D level were assessed to all subjects. The deficiency of vitamin D was more prevalent in diabetic cases than in control cases. There was significant difference between control and diabetic patients in genotyping of FokI (VDR 2228570 C) and TaqI (VDR rs731236 T) polymorphisms. The results of our study revealed that vitamin D deficiency could be a contributing factor for T2DM rising among Egyptian patients. Additionally, there was a genetic variation in the VDR genes FokI and TaqI related to diabetic mellitus in Egyptian patients. Manuscript profile

One of the most common causes of acute liver failure is acetaminophen overdose. The antidote N-acetylcysteine acts by scavenging the reactive metabolite, but its therapeutic limitation necessitates the development of additional therapeutic approaches that can benefit late-presenting patients. Glutathione (GSH) is the most abundant intracellular nonprotein thiol that has an important role in the regulation of many cellular physiologic functions such as redox-homeostatic buffering. This study aims to evaluate the efficacy of GSH supplementation in the recovery of deteriorated liver functions in induced acute acetaminophen toxicity rats; in addition to determining its value in the preservation of DNA integrity in such toxicity. This experimental study was done on 36 albino rats which were divided into three groups (n=12 rats / group) as follows, group1: Control group, group 2: Acetaminophen (APAP) treated group, group 3: APAP and glutathione treated group. Each group was subdivided into 2 subgroups (n=6) and they were sacrificed at 12 hours and 24 hours sequentially. The extent of hepatic inflammation, oxidative stress, and DNA damage was evaluated using histopathological study, and comet analysis, and biochemical markers (ALT, GSH, and MDA). GSH supplementation (APAP and glutathione treated group) significantly improved liver functions resulting in; a statistically significant decrease in ALT levels, reducing Malondialdehyde (MDA) levels, and preserving DNA integrity. GSH is a highly effective alternative in the treatment of APAP hepatotoxicity. Manuscript profile