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Toxicology and Industrial Health, Vol. 23, No. 1, 25-37 (2007)
DOI: 10.1177/0748233707072490

Altered cholinergic metabolism and muscarinic receptor linked second messenger pathways after chronic exposure to dichlorvos in rat brain

Geetu Raheja

Department of Biochemistry, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Kiran Dip Gill

Department of Biochemistry, Post Graduate Institute of Medical Education and Research, Chandigarh, India, kdgill2002{at}yahoo.co.in

Chronic dichlorvos exposure (6mg/kg b.wt/day) for a period of 8 weeks resulted in significant reduction in body weight gain of the male Wistar rats. However, the dietary intake remained unchanged in experimental animals following dichlorvos treatment. Activity of the synthesizing enzyme of acetylcholine (ACh) ie, choline acetyltransferase, was found to be significantly increased and the activity of hydrolyzing enzyme, acetyl cholinesterase (AChE), was inhibited in all the three brain regions studied. Chronic dichlorvos treatment also caused significant reduction in both high affinity (HA) and low affinity (LA) choline uptake (CU), with maximal effect being observed in the brain stem followed by cerebellum and cerebrum. Muscarinic receptor binding was significantly decreased in brain stem and cerebellum as reflected in the decreased receptor number (Bmax), without any change in the binding affinity (Kd) of the receptors. Dichlorvos treatment caused marked inhibition in cAMP synthesis as indicated by decreased adenylate cyclase activity as well as cAMP levels in cerebrum, cerebellum and brain stem. Our study shows that organophosphates may interact with muscarinic receptor-linked second messenger system and this could be a potential mechanism for the neurotoxic effects observed after repeated exposure to low levels of organophosphates, which are unexplainable on the basis of cholinergic hyperactivity. Toxicology and Industrial Health 2007; 23: 25—37.

Key Words: dichlorvos • OP neurotoxicity • muscarinic receptors • second messenger systems • AChE • cholinergic metabolism


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