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1.
Folia Neuropathol ; 53(1): 69-79, 2015.
Article in English | MEDLINE | ID: mdl-25909877

ABSTRACT

Stress induces structural and behavioral impairments. The changes in dendrites and neurons are accompanied by impairments in the tasks mediated by the medial prefrontal cortex (mPFC). The present study was conducted to evaluate the structural changes of the dendrites and neurons of the mPFC after stress using stereological methods. In addition, the effects of a natural and a synthetic substance, i.e., curcumin and sertraline, were evaluated. The rats were divided into 7 groups: stress + distilled water, stress + olive oil, curcumin (100 mg/kg/day), sertraline (10 mg/kg/day), stress + curcumin, stress + sertraline, and control groups. The animals were submitted to chronic variable stress for 56 days. The results showed an average 15% reduction in the length of the dendrites per neuron in the mPFC after stress (p < 0.004). The total spine density was reduced by 50% in the stress (+ olive oil or + distilled water) groups in comparison with the control group (p < 0.01). The main reduction was seen in the thin and mushroom spines, while the stubby spines remained unchanged. Mean volume and surface area of the neurons were decreased by 14% and 10% on average in the stress (+ distilled water or + olive oil) rats in comparison to the control rats, respectively (p < 0.01). The data revealed that treatment of stressed rats with curcumin or sertraline can prevent the loss of spines and reduction of dendrite length, volume and surface area of the neurons. Sertraline and curcumin can prevent structural changes of the neurons and dendrites induced by stress in the mPFC of rats.


Subject(s)
Curcumin/administration & dosage , Dendrites/pathology , Neurons/pathology , Prefrontal Cortex/pathology , Sertraline/administration & dosage , Stress, Psychological/pathology , Animals , Dendrites/drug effects , Drug Therapy, Combination , Male , Neurons/drug effects , Neuroprotective Agents/administration & dosage , Prefrontal Cortex/drug effects , Rats , Rats, Sprague-Dawley , Stress, Psychological/complications , Stress, Psychological/prevention & control
2.
Folia Biol (Praha) ; 60(6): 275-80, 2014.
Article in English | MEDLINE | ID: mdl-25629268

ABSTRACT

Sodium metabisulphite is used as an antioxidant agent in many pharmaceutical formulations. It is extensively used as a food preservative and disinfectant. It has been demonstrated that sulphite exposure can affect some organs. Curcumin, the main element of Curcuma longa, has been identified to have multiple protective properties. The present study extends the earlier works to quantitative evaluation of the effects of sulphite and curcumin on the heart structure using stereological methods. In this study, 28 rats were randomly divided into four experimental groups. The rats in groups I to IV received distilled water (group I), sodium metabisulphite (25 mg/ kg/day) (group II), curcumin (100 mg/kg/day) (group III), and sodium metabisulphite+curcumin (group IV), respectively, for 8 weeks. The left ventricle was subjected to stereological methods to estimate the quantitative parameters of the myocardium. A 20 % decrease was observed in the total volume of ventricular tissue in the sulphite-treated animals compared to the distilled water treatment (P < 0.02). Also, the volume and length of the capillaries were reduced by 43 % on average in the sulphite-treated rats in comparison to the distilled water-treated animals (P < 0.02). However, no significant change was seen in the mean and total volume of the myocardium and the cavity and diameter of the capillaries after sulphite ingestion. Treatment with curcumin did not protect the animals against the structural changes of the ventricle. Sulphite, as a preservative food agent, reduced the length and volume of the ventricular capillaries and curcumin could not protect them.


Subject(s)
Capillaries/drug effects , Coronary Vessels/drug effects , Curcumin/pharmacology , Food Preservatives/toxicity , Heart Ventricles/drug effects , Sulfites/toxicity , Animals , Capillaries/ultrastructure , Cell Size , Connective Tissue/drug effects , Connective Tissue/ultrastructure , Coronary Circulation/drug effects , Coronary Vessels/ultrastructure , Male , Microcirculation/drug effects , Myocardium/ultrastructure , Myocytes, Cardiac/drug effects , Myocytes, Cardiac/ultrastructure , Organ Size , Random Allocation , Rats , Rats, Sprague-Dawley
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