Kalpaamruthaa (KA), a modified indigenous Siddha formulation constitutes Semecarpus anacardium nut milk extract, Emblica officinalis and honey. KA is evaluated for its behavioral and toxicological effects and also its consequence on biochemical and histological variations. Acute and subacute toxicity studies with KA were done on Wistar Albino rats. During acute toxicity study (72 hr), there were no any adverse effects found in the general behavior and mortality at any dose level given (50-2000 mg/kg b.wt.). In subacute toxicity study (30 days) KA (50, 100, 250 and 500 mg/kg b.wt.) did not cause any changes in hematological and biochemical parameters with the exception of a transient rise in hemoglobin, leukocyte count, free fatty acid, plasma and urine creatinine and a significant decrease in blood glucose, total cholesterol, triglyceride and phospholipid levels. The changes observed are significant only at the highest dosage of 500 mg/kg b.wt. Further, histopathological examination of vital organs showed normal architecture suggesting no morphological disturbances; it can be considered that KA is safe and non toxic.
Mitochondria are the major intracellular organelles producing ATP molecules via the electron transport chain. Cancer cells have a deviant energy metabolism, and a high rate of glycolysis is related to a high degree of dedifferentiation and proliferation. The overall net ATP production is diminished with cancer, which ultimately leads to cancer cachexia. The present study was designed to investigate the altered energy metabolism in cancer cells and to enhance ATP production in the normal host cell metabolism by enhancing the activities of mitochondrial enzymes, using energy-modulating vitamins, and thus prevent cancer cachexia. Female Sprague-Dawley rats were selected for the experimental study. Mammary carcinoma was induced by the oral administration of 7,12-dimethylbenz[a]anthracene (25 mg/kg body weight), and treatment was started by the oral administration of the energy-modulating vitamins riboflavin (45 mg/kg body weight per d), niacin (100 mg/kg body weight per d) and coenzyme Q 10 (40 mg/kg body weight per d) for 28 d. Mitochondria were isolated from the mammary gland and liver of all four groups, and the Krebs cycle and oxidative phosphorylation enzymes were assayed. In mammary carcinoma-bearing animals, the activities of the Krebs cycle and oxidative phosphorylation enzymes were significantly decreased. These activities were restored to a greater extent in animals treated with energy-modulating vitamins. From these experimental results, one may hypothesize that the combination therapy of energy-modulating vitamins could be of major therapeutic value in breast cancer.
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