[Interaction of long term calorie restriction and aerobic training programs on serum and tissue concentrations of adiponectin in male obese rats]

Introduction: the aim of present study was to investigate the interaction of aerobic training and calorie restriction on levels of adiponectin isomers in serum and abdominal fat depots in obese male rats

Materials and Methods: forty-eight wistar male rats were used as the study sample. Blood and tissue samples were collected at the 1[st], 18[th] and 28[th] weeks. After baseline sampling, the remaining 40 rats were randomly divided into control and high-fat-diet groups. The high-fat-diet group received their regimen for 18 weeks and were then randomly divided into the negative energy balance [NEB] and high-fat-diet [HFD] subgroups. NEB group alternately underwent 25% calorie restriction or aerobic training [running] with an intensity of 70 to 75% of vo2max for 10 weeks

Results: compared to the standard diet, HFD feeding increased weight and decreased retroperitoneal adipose tissue adiponectin level at the 18[th] and 28[th] weeks [P<0.05]. In comparison to the HFD, group negative energy balance in obese male rats, caused weight control with significant increase in serum levels of total and high-molecular-weight adiponectin as well as adiponectin levels in retroperitoneal and mesenteric fat depots [P<0.05]. Also insulin resistance index in line with serum concentrations of insulin, glucose and triglycerides were decreased in negative energy balance, compared to the high-fat-diet group [P<0.05]

Conclusion: this study indicates that even with simultaneous consumption of high-fat-diet, combination of aerobic training and calorie restriction can increase concentrations of adiponectin in serum and abdominal fat depots of obese male rats, and aligned with it improves lipid and metabolic profiles

[Buserelin inhibits apoptosis in male germ cells induced by busulfan in mouse testis]

The aim of this study was to investigate the effect of buserelin on apoptosis of male germ cells induced by busulfan in adult male mice. Male adult NMRI mice were divided into four group of eight each. Group 1 [control] administered PBS for 21 days subcutaneously, group 2 given 0.4 micro g buserelin for 21 days subcutaneously, group 3 given single dose of 30 mg/kg busulfan intraperitoneally and group 4 given both busulfan and buserelin for 21 days. The animals were sacrificed and their testes were dissected 35 days after the treatment. Evaluations were made by determining Johnson's score and apoptosis were assayed by terminal- deoxynucleotidyl- transferase-mediated dutp nick end labeling [TUNEL]. Statistical analyses were performed using ANOVA test. Recovery status and Johnson's score in group 4 were significantly higher than those of busulfan treated group 7.71 +/- 0.69 VS 4.46 +/- 0.56 [p< 0.001]. Apoptotic cells number cells were significantly more numerous in busulfan treated group than those of control 23.28 +/- 7.10 VS 3.54 +/- 1.02 [p<0.001]. While buserelin substantially reduced germ cell apoptosis in fourth group 10.50 +/- 2.91 in comparison with third group 23.28 +/- 7.10, [p<0.001]. Administration of buserelin after testicular damage by busulfan enhances the regeneration of spermatogenesis in mouse through inhibition of apoptosis in germ cells

[Effect of fibroblastic growth factor on resumption of meiosis, in vitro maturation and embryo development of immature mouse oocytes]

The purpose of this study was to evaluate the effect of fibroblastic growth factor on resumption of meiosis, in vitro maturation of immature mouse oocytes and resulting embryo development with and without basic fibroblastic growth factor-4 [bFGF-4].Cumulus - oocyte complex [COCs] and germinal vesicle [GV] were obtained from female NMRI mice 46-48 hours after administration of an intra-peritoneal injection of 5 IU PMSG. COCs were cultured in TCM199 supplemented with different dosages of bFGF-4. After 24 hours, metaphase II [MII] oocytes were co-incubated with sperms for 4-6 hours in 16 medium. For all groups, the rate of cleaved embryos was assessed in the T6 medium until blastocyst stage. In all compared groups, the percentage of matured MII oocytes in the 10 ng/ml [%94.4] and 20 ng/ml [%92.5] of bFGF-4 treatment groups, was significantly higher [P<0.05] than those of the control group but the percentage of embryos that developed to blastocyst in 20 ng/ml bFGF-4 treatment group was significantly higher than those of the control group [P<0.05]. Exogenous bFGF-4 improved the oocyte maturation and embryo development