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1.
Clin Exp Hypertens ; 35(5): 373-81, 2013.
Article in English | MEDLINE | ID: mdl-23072377

ABSTRACT

In this study, experimental diabetes and nephrectomy have been applied separately and together in order to investigate the possible therapeutic effects of lipoic acid (LA) on hypertensive and diabetic rat kidneys. Wistar rats were divided into eight groups: control, diabetes mellitus (DM), 5/6 nephrectomy, DM + 5/6 nephrectomy, LA administration, DM + LA treated, 5/6 nephrectomy + LA treated, and DM + 5/6 nephrectomy + LA-treated groups, respectively. Renal damage was evaluated histomorphometrically, ultrastructurally, and biochemically. Our findings supported that diabetes and hypertension together increased the rate of renal injury, and LA had therapeutic effects on hypertensive and diabetic rat kidneys.


Subject(s)
Diabetes Mellitus, Experimental/drug therapy , Hypertension/drug therapy , Thioctic Acid/therapeutic use , Animals , Diabetes Mellitus, Experimental/chemically induced , Diabetic Nephropathies/prevention & control , Disease Models, Animal , Hypertension/etiology , Male , Nephrectomy/adverse effects , Rats , Rats, Wistar , Streptozocin/adverse effects
2.
Acta Histochem ; 109(6): 480-5, 2007.
Article in English | MEDLINE | ID: mdl-17698173

ABSTRACT

Aging is accompanied by significant structural and functional transformations of all organs and systems. Age-associated increase in apoptotic behavior may cause disease. Older cells are more susceptible to endogenous oxidative damage, and oxidative stress is a potent inducer of apoptosis. Deprenyl is an irreversible monoamine-oxidase B inhibitor which has anti-oxidant, anti-apoptotic and neuroprotective effects. Estrogen is also a neuroprotective and anti-oxidant hormone. The objectives of this study were to determine whether the anti-oxidative effects of deprenyl can suppress apoptotic activity, with or without estradiol, in aged female rat livers. In this study, ovariectomized female Wistar albino rats were divided into six groups as follows; young (3 months old) saline-treated control, aged (24 months old) saline-treated control, aged deprenyl treated, aged estradiol treated, aged deprenyl plus estradiol treated and aged sham controls. All rats except for the sham group were treated for 21 days. Determination of oxidative stress parameters was performed spectrophotometrically. To detect apoptotic cells, TUNEL staining was performed. The results were analyzed by one-way ANOVA post hoc Bonferroni test. Deprenyl and estradiol administration, alone or in combination, decreased significantly the levels of lipid peroxidation and increased superoxide dismutase activity in the liver relative to aged control and sham rats (P<0.05). The number of TUNEL positive cells decreased significantly in deprenyl and estradiol-treated rats compared with aged control and sham rats. The results indicate that deprenyl treatment alone, or in combination with estradiol, may modulate age-related apoptotic changes in rat liver by decreasing oxidative stress.


Subject(s)
Aging , Apoptosis/drug effects , Estradiol/pharmacology , Liver/drug effects , Oxidative Stress/drug effects , Selegiline/pharmacology , Animals , Female , In Situ Nick-End Labeling , Lipid Peroxidation/drug effects , Liver/cytology , Liver/metabolism , Ovariectomy , Rats , Rats, Wistar , Thiobarbituric Acid Reactive Substances/metabolism
3.
Brain Res ; 982(1): 125-30, 2003 Aug 22.
Article in English | MEDLINE | ID: mdl-12915247

ABSTRACT

We investigated whether the psychostimulant methamphetamine (METH) has a cytotoxic effect on oligodendrocytes and which cell-death pathways are involved in the cytotoxic process. METH caused concentration- and time-dependent cytotoxicity in rat oligodendrocyte cultures. METH induced apoptotic cell death and mRNA expression of pro-apoptotic proteins (bax and DP5), but not anti-apoptotic proteins (bcl-2 and bcl-XL). These results suggest that METH induces cytotoxicity in rat oligodendrocytes via the differential regulation of the expression of genes involved in the apoptotic process.


Subject(s)
Apoptosis , Cytotoxins/pharmacology , Methamphetamine/pharmacology , Oligodendroglia/drug effects , Oligodendroglia/physiology , Animals , Apoptosis Regulatory Proteins , Neuropeptides/genetics , Oligodendroglia/metabolism , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins c-bcl-2/genetics , RNA, Messenger/metabolism , Rats , Rats, Wistar , bcl-2-Associated X Protein , bcl-X Protein
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