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1.
Acta Physiol Hung ; 95(1): 65-76, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18389999

ABSTRACT

The aim of this work was to evaluate the effect of prolonged melatonin administration on chosen metabolic and hormonal variables in male and female Sprague-Dawley rats. Melatonin was administered in tap water (4 microg/ml) daily from the 6th month of age. Rats were fed a standard type of diet ad libitum and were kept in a light regimen L:D--12:12h. The experiment was terminated after 12 weeks of melatonin administration. Melatonin decreased body mass during the whole experiment in females and from the 42nd day of the experiment in males. Relative heart muscle weight in females and absolute/relative thymus weight in males were increased after melatonin administration. Melatonin decreased glycaemia, heart muscle glycogen concentration in females and liver glycogen concentration in both sexes. Serum insulin concentration in males was decreased; serum corticosterone concentration was increased in both males and females. Serum triacylglycerol and heart muscle cholesterol concentration in females were decreased, however in males serum and heart muscle cholesterol concentration was increased. Liver phospholipid concentration in females was decreased and heart muscle phospholipid concentration in males was increased. Melatonin increased malondialdehyde concentration in heart muscle in males and in liver in both sexes. Melatonin induced prominent sex-dependent changes in both carbohydrate and lipid metabolism.


Subject(s)
Body Weight/drug effects , Lipid Metabolism/drug effects , Melatonin/administration & dosage , Organ Size/drug effects , Animals , Cholesterol/analysis , Circadian Rhythm , Corticosterone/blood , Female , Glycemic Index/drug effects , Glycogen/analysis , Insulin/blood , Liver/drug effects , Liver/metabolism , Male , Malondialdehyde/analysis , Myocardium/metabolism , Phospholipids/analysis , Rats , Rats, Sprague-Dawley , Sex Factors , Thymus Gland/metabolism , Triglycerides/blood
2.
Neoplasma ; 54(3): 251-5, 2007.
Article in English | MEDLINE | ID: mdl-17447859

ABSTRACT

The aim of the present study was to determine whether prolonged stress repeated immobilization in boxes during the period of 18 weeks (IMS) influenced development and progression of N-methyl-N-nitrosourea (NMU)-induced mammary tumors in female Sprague-Dawley rats and whether long-term MEL application affected changes caused by stress. NMU was applied intraperitoneally in two doses each of 50 mg/kg b.w. between 40-50 postnatal days. Melatonin (MEL) was administered in drinking water in a concentration of 4 microg/ml (daily from 3 p.m to 8 a.m), application was initiated 3 days prior to first NMU dose and lasted until the end of the experiment. Immobilization (2 h/day) began on the fifth day after second carcinogen application, animals were immobilized three times a week. Repeated immobilization of rats during 18 weeks decreased tumor frequency per group and per animal by 30% and tumor volume gain by 16% as opposed to control (NMU) animals. Combination of repeated immobilization and a long-term MEL application lowered incidence by 13% when compared to control, prolonged latency by 13%, decreased tumor frequency per group (by 44%) and per animal (by 35%). Tumor volume gain increased by 35% but their cumulative volume prominently decreased by 74% as opposed to control. Tumor volume was the most markedly influenced by MEL, induced tumors developed more rapidly tumor volume gain increased by 61%. However, their cumulative volume markedly decreased by 75% when compared to immobilized group drinking water. Prolonged stress inhibited development and progression of NMU-induced mammary gland tumors in female rats and this effect was enhanced by long-term melatonin administration.


Subject(s)
Antioxidants/therapeutic use , Mammary Neoplasms, Experimental/prevention & control , Melatonin/therapeutic use , Stress, Psychological , Animals , Carcinogens/toxicity , Female , Mammary Neoplasms, Experimental/chemically induced , Methylnitrosourea/toxicity , Rats , Rats, Sprague-Dawley
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