Anti-diabetic effect of balanites aegyptiacea leaves extract [HEGLIG] by regulation of erythrocyte glucose uptake in diabetic patients type 2 in vitro

Background: in Diabetes, the increase in the oxidative stress and decrease in the antioxidant defense may elevate he susceptibility of diabetic patients to many pathological complications, oxidative induced cell damage has been proposed to play an important role in the etiology of numerous pathological conditions. So, the aim of the present study was to investigate the antioxidant potential of Alcoholic Leaves extract of Balanites aegyptiacea [Heglig] due to the presence of phenolic and flavonoids compounds on uptake of glucose in vitro by erythrocytes of diabetic patients

Results: in hyperglycemic patients, erythrocytes malondialdehyde level was highly significantly increased [P<0.0001] than that of control. However, the erythrocytes glutathione content was highly significantly decreased [P< 0.0001] when compared to that of corresponding control values. The glucose uptake by erythrocytes of diabetic patients was highly significantly decreased [P < 0.0001] with increasing hyperglycemia [Fasting Blood glucose], while it was highly significantly elevated [P< 0.0001] after addition of Balanites aegyptiacae leaves extract to the incubation medium. On the other hand, the malondialdehyde concentration was highly significantly reduced [P < 0.0001] on adding the extract. So, it could be concluded that, an appreciate support for enhancing Antioxidant supply from natural sources such Balanites aegyptiace leaves extract may help control blood glucose levels and prevent pathological complications of diabetes

Influence of adipose tissue derived mesenchymal stem cells in combination with injectable bone substitute on osteoclastogenesis in osteoporotic rats.

The present study was designed to evaluate the influence of adipose tissue derived mesenchymal stem cell (ASCs) with or without calcium phosphate composite on osteoclastogenesis in osteoporotic rats. Mesenchymal stem cells (MSCs) were harvested from adipose tissue of both the omentum and the inguinal fat pad of male rats, as the sex mismatch, to track the MSCs fate and to ensure their homing to the injured females' femurs. The isolated ASCs were characterized via the morphological appearance, multilineage potential and the PCR detection of CD29, CD44, CD106, CD14, CD34 and CD45 surface markers. Fifty adult female albino rats were enrolled in the current study. The rats were classified into five groups: group 1 was the gonad intact control, group 2 served as untreated ovariectomized (OVX) rats, group 3 was OVX rats treated with ASCs, group 4 was OVX rats treated with ASCs with injectable bone substitute (IBS) and group 5 was OVX rats treated with IBS. The serum levels of osteoprotegerin (OPG) and receptor activator of NF-қβ ligand (RANKL) were assayed using ELISA procedure. In addition, nuclear factor-κβ (NF-κβ) gene expression level was estimated in femur bones using real time –PCR. The isolated ASCs proved their MSCs identity via their morphological appearance and multilineage potential. In addition, the isolated ASCs showed positive expression for CD29, CD45, CD44 as well as CD106 and negative expression for CD34 and CD14. Besides, the positive expression of the Y-chromosome (sry) gene detected in the ASCs treated groups indicated that the systemically delivered single dose of undifferentiated ASCs was able to home at the females' femur bones. Adipose tissue derived mesenchymal stem cells (ASCs) injection with or without calcium phosphate composite in OVX rats reversed the effect of ovariectomy on the studied biomarkers causing significant increase in serum OPG level accompanied with significant decrease in serum RANKL level. Also, significant down regulation of NF-κβ gene expression in femur bones was detected in the treated groups compared with untreated OVX group. These results clarified the good influence of ASCs against osteoclastogenesis. In addition the combination of ASCs injection with osteoinductive material injectable calcium phosphate composite (IBS), may be useful to achieve the significant antiosteoporotic effects.

Molecular genetic and biochemical evaluation of ghrelin hormone as a novel signal of gonadal function in adult male rats

It is well known that reproductive function is regulated by the interplay of the hypothalamus, pituitary and gonads, which form the so called reproductive axis. A number of factors primarily involved in the control of energy balance and metabolism have been proven as putative modulators of the gonadal axis, thus providing the basis for the link between energy homeostasis and fertility. Ghrelin is a 28 amino acid peptide. It is predominantly produced by the endocrine X/ A- like cells of the stomach submucosa and mobilized by food deprivation. Ghrelin concentrations were observed to change with fasting and refeeding in mammals. The potential reproductive role of ghrelin has received attention recently. The Objective of this work is to study the effect of chronic food restriction on ghrelin level in adult male rats and it's relation to reproductive hormones. The present study was carried out on 32 adult male Sprague Dawley rats divided into 4 groups: Group I [control group] comprised 8 rats fed ad libitum for 30 days, Group II, III and IV [food-restricted groups for 10, 20 and 30 days respectively] each consisted of 8 rats fed 50% of ad libitum intake determined by the amount of food consumed by the control group. Mean body weight of food restricted rats was observed to decrease during the period of the experiment. Food restriction produced significant increase of serum ghrelin with significant decrease of both gastric and hypothalamic ghrelin accompanied with significant increase in its gene expression in stomach and hypothalamus. Testosterone, follicle- stimulating hormone [FSH] and luteinizing hormone [LH] levels showed significant decrease correlated with down- regulation of gonadotropins, aromatase and kisspeptin [Kissl] genes in food restricted rats compared with control group. Ghrelin could be one of the hormones responsible for the suppression of male reproductive axis in case of negative energy balance. Thus, ghrelin could provide a link between energy homeostasis and reproductive capacity in adult male rats

Potential antidiabetic and hypolipidemic effects of propolis extract in streptozotocin-induced diabetic rats

Free radicals have been implicated in the pathogenesis of diabetes mellitus leading to various complications including atherosclerosis. Propolis was reported to have oxygen radical scavenging activity. The present study was designed to investigate the possible antidiabetic, hypolipidemic and antioxidant effects of ethanolic extract of propolis [EEP]. Type[2] diabetes was induced in rats by injection of streptozotocin [STZ] in a dose of 60 mg/kg bwt, i.p. for 3 consecutive days. After 5 weeks of STZ injection, there were an apparent reduction in the animal body weight amounting to 21% and significant increases in serum glucose [184%], triglycerides [63%], total cholesterol [43%] and low density lipoprotein-cholesterol [LDL-C] [148%] with a concomitant decrease in serum high density lipoprotein-cholesterol [HDL-C] [51%] as compared to the control normal group. In addition, there was significant elevation in pancreatic lipid peroxides measured as malondialdehyde [MDA] and serum nitric oxide [NO] amounting to 185% and 224%, respectively with marked reduction in serum reduced glutathione [GSH] andcatalase [CAT] [66% and 31%, respectively] and pancreatic superoxide dismutase [SOD] [54%] in STZ-treated rats. On the other hand, oral daily treatment of animals with EEP in a dose of 200mg/kg bwt for a period of 5 weeks ameliorated STZ-induced alterations in the animal body weight as well as in serum glucose, lipids, lipoproteins, NO, GSH and CAT and pancreatic MDA and SOD. In conclusion, propolis extract offers promising antidiabetic and hypolipidemic effects that may be mainly attributed to its potent antioxidant potential. Further studies will be needed in future in order to determine which one[or more] of its active constituents has the main antidiabetic and hypolipidemic effects

effects of oral grape seed extract on cisplatin-induced cytogenotoxicity in mice

The present investigation was directed to study the possible chemoprotective activity of orally administered grape seed extract [GSE] against cisplatin-induced cytotoxicity and genotoxicity towards mouse somatic and germinal cells in vivo. Pretreatment of mice with GSE [100 mg/kg/day] for 7 days and simultaneously with a single dose of cisplatin [2.2 or 5.5 mg/kg, i.p.] for another day, significantly reduced the frequency of bone marrow micronucleated polychromatic erythrocytes by factors of 1.9 and 1.28, respectively. Furthermore, GSE caused a reduction in bone marrow suppression induced by cisplatin treatment, particularly before the lower dose. In male germline, orally administration of GSE [100 mg/kg/day] for 7 consecutive days before and 7 consecutive days after treatment with a single dose of cisplatin [2.2 or 5.5 mg/kg, i.p.], significantly elevated the levels of sperm motility reduced by cisplatin treatment. Furthermore, GSE significantly decreased the elevated levels of sperm head abnormality induced with cisplatine by factors of 1.6 and 1.2, respectively. Our results indicate that GSE plays a role in attenuating the genotoxicity induced by cisplatin and may provide decreases in the development of secondary malignancy and abnormal reproductive outcomes risks

Protective effect of captopril against cisplatin induced nephrotoxicity in rats

This study has been initiated to determine whether captopril, an angiotensin-converting enzyme [ACE] inhibitor containing sulfhydryl [-SH] group can protect against cisplatin-induced nephrotoxicity in rats. A single dose of cisplatin [7.5mg/kg bwt] injected i.p. caused a significant increase in blood urea nitrogen [BUN] and creatinine levels amounting to 402% and 573%, respectively with a marked elevation in lipid peroxides measured as malondialdehyde [MDA] content [54%], accompanied by a significant decrease in reduced glutathione [GSH] content [27%] of kidney tissue as compared to control group. In addition, there were marked increases in kidney tissue content of nitric oxide [NO] [43%] and plasma endothelin-1[ET-1] [37%]. On the other hand, administration of captopril [60mg/kg bwt, i.p.] 1 h before cisplatin protected the kidney as indicated by restoration of BUN, creatinine, MDA, GSH, NO and ET-1. These results indicate that captopril, an ACEI, has a protective effect against cisplatin-induced damage to kidney. This reflects the beneficial role of captopril in treatment of renovascular hypertention and congestive heart failure; an effect that may be related to its free radicals scavenging and antioxidant effects which are sulfhydryl dependent

Hesperidin, an antioxidant flavonoid, prevents acrylonitrile-induced oxidative stress in rat brain

Acrylonitrile [ACN] is a volatile, toxic liquid used as a monomer in the manufacture of synthetic rubber, styrene plastics, acrylic fiber and adhesives. ACN is a potent neurotoxin. A role for free radical-mediated lipid peroxidation in the toxicity of ACN has been suggested. We examined the ability of hesperidin, an antioxidant flavonoid, to attenuate ACN-induced alterations in lipid peroxidation in rat brains. The daily oral administration of ACN to male albino rats in a dose of 50 mg/kg bwt for a period of 28 days produced a significant elevation in brain lipid peroxides measured as malondialdehyde [MDA] amounting to 107%, accompanied by a marked decrease in brain reduced glutathione [GSH] content reaching 63%. In addition, ACN administration resulted in significant reductions in the enzymatic antioxidant parameters of brain; superoxide dismutase [SOD], catalase [CAT], glutathione peroxidase [GSH-Px] and glutathione-S-transferase [GST] recording 43%, 64%, 52% and 43%, respectively. On the other hand, pretreatment with hesperidin and its co-administration with ACN once daily in a dose of 200 mg/kg bwt, i.p. for 28 days ameliorated ACN-induced alterations in brain lipid peroxidation. These results suggest that hesperidin may have a beneficial role against ACN-induced oxidative stress in brain; an effect that is mainly attributed to the antioxidant property of hesperidin

effect of thiola, piroxicam and diltiazem on the uterine contratility of gamma-irraidated rats

Accidental radfiation exposure raises concern for functional modifications in the uterine physiology. In the current work, total body gamma-irradiation [0.7, 1.4 and 2.1 Gy] of non-pregnant adult female albino rats increased significantly the frequency and amplitude of uterine contractions in-vivo. Administration of Thiola [a sulghydryl containing agent] in doses of 100 or 250 mg/kg, pre-irradiation, or Piroxicam [a potent prostaglandin inhibitor] in a dose of 2 mg/kg, pre- or post-irradiation failed to normalize the changes induced by gamma-irradiation. However, administration of Diltiazem [a Ca+2 channel blocker, 8 mg/kg] pre- or post-irradiation caused significant decrease in the frequency of uterine contractions [21% and 24% respectively] as well as the amplitude of contractions [62% and 39 respectively] in comparison to the uterotonic pattern of gamma-irradiation alone. The results indicate a promising tocolytic activity of Diltiazem against the uterotonic effect of gamma-radiation