Effect of Melatonin on Glutamate: BDNF Signaling in the Cerebral Cortex of Polychlorinated Biphenyls (PCBs)—Exposed Adult Male Rats

• Published in: Neurochemical research Vol. 40; no. 9; pp. 1858 - 1869
• Main Authors: Bavithra, S., Sugantha Priya, E., Selvakumar, K., Krishnamoorthy, G., Arunakaran, J.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.09.2015; Springer Nature B.V
• Subjects: Animals; Biochemistry; Biomedical and Life Sciences; Biomedicine; Brain-Derived Neurotrophic Factor - genetics; Brain-Derived Neurotrophic Factor - metabolism; Calcium Channels, N-Type - metabolism; Calpain - metabolism; Cell Biology; Cerebral Cortex - drug effects; Cerebral Cortex - enzymology; Cerebral Cortex - metabolism; Cyclic AMP Response Element-Binding Protein - genetics; Cyclic AMP-Dependent Protein Kinases - metabolism; Glutamic Acid - metabolism; Male; Melatonin - pharmacology; Neurochemistry; Neurology; Neurosciences; Original Paper; Polychlorinated Biphenyls - toxicity; Rats; Receptors, Glutamate - metabolism; RNA, Messenger - genetics; Signal Transduction; PCBs; Cerebral cortex; Neurotoxicity; Melatonin; Glutamate; BDNF
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-015-1677-z

Various epidemiological survey suggests that the central nervous system is the target for many environmental contaminants. One among them is Aroclor 1254, a mixture of polychlorinated biphenyls (PCBs) which explore a spectrum of biochemical and neurotoxic responses in humans and laboratory animals. Learning and motor coordination deficits are the profound effects of PCBs which may be related to cerebral dysfunction. The aim of the study is to elicit the protective effect of melatonin (Mel), a potent, blood brain permeable antioxidant against the effect of Aroclor 1254 on the signaling of glutamate—principal excitatory neurotransmitter and brain derived neurotrophic factor (BDNF) in the cerebral cortex of adult rats which plays a key role in brain functions. Adult male Wistar rats were grouped into four and treated intraperitonealy (i.p) Group I with corn oil (Control), Group II with PCBs (2 mg/kg/bwt), Group III with PCBs + Mel (2 mg/kg/bwt + 5 mg/kg/bwt) and Group IV with Mel (5 mg/kg/bwt). The protein expression of glutamate signaling molecules and mRNA expressions of GLAST, BDNF signaling molecules were analyzed. The results suggest that simultaneous melatonin treatment significantly attenuated the NMDA receptor mediated glutamate excitotoxicity and protects the inhibition of BDNF signaling caused by PCBs exposure in cerebral cortex of adult male rats. Graphical Abstract Schematic pathway illustrating the proposed mechanism by which melatonin protects against A1254 mediated glutamate induced neurodegeneration in the cerebral cortex of adult male rats. PCBs induced neurodegeneration is caused by the overactivation of NMDAR, followed by the activation of voltage dependent calcium channels leading to the increase in intracellular Ca 2+ that stimulates calpain. Calpain inturn inhibits the PKA α and neurtrophin BDNF, its receptor and downstream signaling MAPK pathway leading to neurodegeneration. Melatonin had scavenged the ROS produced by PCBS and decreased the NMDAR expression which inturn protected the cells from neurodegeneration.