Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add filters








Language
Year range
1.
J Environ Biol ; 2006 May; 27(2 Suppl): 355-8
Article in English | IMSEAR | ID: sea-113696

ABSTRACT

The toxicity of sub-acute inhalation of mosquito repellent mat vapour exposure 3 hr daily, either for a duration of 15 days (Group II) or for 30 days (Group III) on biochemical parameters in serum and vital organs was evaluated in mice. The control animals were exposed to ambient air 3 hr daily, either for 15 days [Group I (a)] or 30 days [Group I (b)]. In both the Group II and Group III exposure studies, elevation in the activity of aspartate transaminase (AST) and alanine transaminase (ALT) was observed in the serum and heart tissue and a decrease in their activity in lung and spleen tissue. This biochemical lesion indicates that exposure to mat vapour is capable of interfering with the metabolism of non-essential amino acids and induce cellular damage in the tissues. The elevation in the activity of AST along with that of lactate dehydrogenase (LDH) observed in serum and heart tissue in Group II and III studies indicate that exposure to mat vapour is capable of inducing changes in the myocardial function. The elevation in the activity of alkaline phosphatase (ALP) in serum and a decrease in its activity in lung and heart tissue of mice exposed to mat vapour for 30 days (Group III) observed in this study denotes that mat vapour could interfere with various metabolic functions to induce derangements at cellular level. Inhalation of hitherto unidentified volatile chemicals emanated from mosquito repellent mat, may contribute as stress factors may contribute as in an indoor environment to produce above mentioned biochemical lesions in vital organs.


Subject(s)
Alanine Transaminase/blood , Animals , Aspartate Aminotransferases/blood , Culicidae , Inhalation Exposure , Insect Repellents/administration & dosage , Lung/drug effects , Mice , Myocardium/metabolism , Spleen/drug effects
2.
J Environ Biol ; 2005 Apr; 26(2): 191-5
Article in English | IMSEAR | ID: sea-113773

ABSTRACT

The activities of phosphatases and transaminases were studied in muscle and liver of the fresh water fish, Oreochromis mossambicus on exposure to different sublethal concentrations (0.25, 0.5, 0.75 and 1 mgl(-1)) of cartap hydrochloride (insecticidal derivative from marine polycheate) for 96 h. There was an overall decrease in phosphatases and transaminases activity in muscle and liver of the fish subjected to cartap hydrochloride.


Subject(s)
Acid Phosphatase/metabolism , Alanine Transaminase/antagonists & inhibitors , Alkaline Phosphatase/metabolism , Animals , Aspartate Aminotransferases/antagonists & inhibitors , Liver/drug effects , Muscles/drug effects , Polychaeta/chemistry , Thiocarbamates/toxicity , Tilapia/metabolism
3.
Indian J Exp Biol ; 2005 Mar; 43(3): 264-7
Article in English | IMSEAR | ID: sea-60944

ABSTRACT

The effect of ethanolic extract of Terminalia arjuna bark on carbohydrate metabolizing enzymes of N-nitrosodiethylamine induced hepatocellular carcinoma in Wistar albino rats were studied. The plasma and liver glycolytic enzymes such as hexokinase, phosphoglucoisomerase, aldolase were significantly increased in cancer induced animals while glyconeogenic enzyme, glucose-6-phosphatase was decreased. These enzymes were reverted significantly to near normal range in treated animals after oral administration of T. arjuna for 28 days. The modulation of the enzymes constitute the depletion of energy metabolism leads to inhibition of cancer growth. This inhibitory activity may be due to the anticancer activity of constituents present in the ethanolic extract of T. arjuna.


Subject(s)
Animals , Carbohydrate Metabolism , Carcinoma, Hepatocellular/chemically induced , Diethylnitrosamine/pharmacology , Ethanol/pharmacology , Liver/metabolism , Liver Neoplasms/chemically induced , Male , Phytotherapy/methods , Plant Bark/metabolism , Plant Structures/metabolism , Plant Extracts/pharmacology , Rats , Rats, Wistar , Terminalia/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL