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

Abstract

Chronic dichlorvos exposure (6 mg/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 (B(max)), without any change in the binding affinity (K(d)) 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.

• Authors: Geetu Raheja, Kiran Dip Gill
• Journal: Toxicology and industrial health (Toxicol Ind Health) Vol. 23 Issue 1 Pg. 25-37 (Feb 2007) ISSN: 0748-2337 [Print] England
• PMID: 17722737 (Publication Type: Journal Article)

Chemical References

• Insecticides
• Receptors, Muscarinic
• Dichlorvos
• Choline O-Acetyltransferase
• Acetylcholinesterase

Topics

• Acetylcholinesterase (drug effects, metabolism)
• Administration, Oral
• Animals
• Brain (drug effects, metabolism)
• Brain Stem (drug effects, metabolism)
• Cerebellum (drug effects, metabolism)
• Choline O-Acetyltransferase (drug effects, metabolism)
• Dichlorvos (toxicity)
• Dissection
• Insecticides (toxicity)
• Male
• Rats
• Rats, Wistar
• Receptors, Muscarinic (drug effects, metabolism)
• Second Messenger Systems (drug effects)
• Synaptosomes (chemistry, metabolism)
• Telencephalon (drug effects, metabolism)
• Weight Gain (drug effects)