Bangladesh Journal of Pharmacology Volume: 11; Number 4; Year 2016 Cite this article as: Rajagopal SS, Swaminathan G, Manickam V, Ramanathan S. Effect of Pedalium murex against lipopolysaccharide-induced neurotoxicity in substantia nigra of rat midbrain. Bangladesh J Pharmacol. 2016; 11: 876-877. Effect of Pedalium murex against lipopoly- saccharide-induced neurotoxicity in substantia nigra of rat midbrain Sir, Parkinson's disease affects approximately 1–3% of the population and is characterized by a slow and progre- ssive degeneration of dopaminergic neurons in the substantia nigra (Obeso et al., 2000). This process is characterized by the progressive loss of dopaminergic neurons in the substantia nigra pars compacta and is accompanied by depletion of striatal dopamine and its metabolites such as DOPAC (3,4 dihydroxy phenyl acetic acid) and HVA (homovanillic acid). Activation of the immune system in response to stress and infection or bacterial endotoxin lipopolysaccharide produces profound neurophysiological, neuroendocrine and behavioral changes. To date, specific pharmacologic agents that can be used in the management of septic shock are lacking and yet a rather scanty number of potential therapeutic agents are under clinical trials (Gallily et al., 1997). Lipopoly- saccharide, among the principal components of all gram -negative bacteria, has been extensively studied as a major factor contributing to the pathogenesis of bacte- rial infections. Endotoxic shock can be elicited by a systemic injection of lipopolysaccharide induces the production and release of several cytokines (Morrison and Ryan, 1987). In response to these cytokines, several reactive oxygen species are produced from cells such as neutrophils and other phagocytic cells, creating a status of oxidative stress (Sugnio et al., 1987). Thus, this type of stress may hypothetically support the assumption that lipopolysaccharide-induced cell injury would be retarded by modifying free radical metabolism with the aid of antioxidant pretreatment. One of the widely used medicinal herbs, in indigenous systems of medicine, is Pedalium murex which belongs to the family Pedaliaceae and commonly known as “Anai nerinji”. Epidemiological studies have suggested posi-tive associations between the consumption of phenolic-rich foods or beverages and the prevention of diseases. The aim of the present study is to examine the effect of ethanolic extract of P. murex in the protection of dopaminergic neurons from lipopolysaccharide- induced neurotoxicity in rats. The plant is authenticated by Botanical Survey of India (No. BSI/SC/5/23/2012-13/Tech-1934). Leaves were dried in shade and extracted with 90% v/v ethanol, the extract used for phytochemical screening. Results showed the presence of flavonoids, alkaloids, carbo- hydrate and proteins. Adult male Sprague-Dawley rats (120) weighing 240- 350 g purchased from the Animal House of J. K. K. N. College of Pharmacy. Rats were kept under standard laboratory conditions with controlled temperature, 12 hours light/dark cycle and given free access to standard diet and water. Animals were acclimatized for one week before starting the in vivo experiment. The experimental protocols were approved by the Institutional Animal Ethical Committee with reference No: 887/ac/15/CPCSEA. The lipopolysaccharide (Escherichia coli-derived; 500,000 endotoxin units/mg) and all chemicals were purchased from Sigma-Aldrich, USA. Group І: Received 0.9% saline vehicle, i.p for 7 days and served as a vehicle; Group II: Received a single i.p injection of lipopolysaccharide (10 mg/kg); Group III: Received single i.p injection of lipopolysaccharide (10 mg/kg) and ethanolic extract of P. murex (100 mg/kg, i.p) for 7 days; Group IV: received single i.p injection of lipopolysaccharide (10 mg/kg) and ethanolic extract of P. murex (200 mg/kg, i.p) for 7 days. After the experimental period, the rats were anesthe- tized then decapitated. Brain was removed and the midbrain was dissected. Each dissected midbrain was weighed and stored at -80°C until time brain tissues were processed for measurement of dopamine and its metabolites. A single intraperitoneal injection of lipopolysaccharide A Journal of the Bangladesh Pharmacological Society (BDPS) Bangladesh J Pharmacol 2016; 11: 876-877 Journal homepage: www.banglajol.info Abstracted/indexed in Academic Search Complete, Agroforestry Abstracts, Asia Journals Online, Bangladesh Journals Online, Biological Abstracts, BIOSIS Previews, CAB Abstracts, Current Abstracts, EMBASE/Excerpta Medica, Google Scholar, HINARI (WHO), International Pharmaceutical Abstracts, Open J-gate, Science Citation Index Expanded, SCOPUS and Social Sciences Citation Index ISSN: 1991-0088; DOI: 10.3329/bjp.v11i4.29306 Letter to the Editor Table I Effect of striatal dopamine and its metabolites Group Dopamine (µg/ g wet tissue) DOPAC (µg/ g wet tissue) HVA (µg/g wet tissue) I 14.9 ± 0.9 1.3 ± 0.2 0.9 ± 0.0 II 9.8 ± 1.1 0.5 ± 0.1 0.4 ± 0.0 III 10.1 ± 1.2 0.7 ± 0.1 0.6 ± 0.0 IV 13.2 ± 0.9 1.1 ± 0.1 0.7 ± 0.0 (10 mg/kg) in male Sprague-Dawley rats resulted in a decrease of dopamine and its metabolites levels compared to the control. Dopamine and its metabolites levels were significantly increased in ethanol extract of P. murex (200 mg/kg) treated rats compared to in the lipopolysaccharide-treated rats. Ethanol extract of P. murex was found to possess potential therapeutic effect against lipopolysaccharide-induced neurotoxicity via preserving dopamine level in nigrostriatal pathway of rat midbrain. In conclusion, the ethanol extract of P. murex may be used for remedy of neurodegenerative disease. Shanmuga Sundaram Rajagopal, Gomathi Swaminathan, Vijayabaskaran Manickam, Sambathkumar Ramanathan J. K. K. Nattraja College of Pharmacy, Komarapalayam, Tamilnadu, India. Corresponding author: email: gomathiswaminathan03@gmail.com References Gallily R, Yamin A, Waksmann Y, Ovadia H, Weidenfeld J, Bar -Joseph, Biegon A, Mecholoulam R, Shohami E. Protection against septic shock and suppression of tumor necrosis factor alpha and nitric oxide production by dexanabinol (HU-211), a non-psychotropic cannabinoid. J Pharmacol Exp Ther. 1997; 283: 918–24. Morrison D, Ryan JL. Endotoxins and disease mechanism. Annu Rev Med. 1987; 38: 417–32. Obeso, JA, Rodriguez-Oroz MC, Rodriguez M, Lanciego JL, Artieda J, Gonzalo N, Olanow CW. Pathophysiology of the basal ganglia in Parkinson's disease. Trends Neurosci. 2000; 23: S8–S19. Sugino K, Dhi K, Yamada K, Kawill Beaki T. The role of lipid peroxidation in endotoxin-induced hepatic damage and the protective effect of antioxidants. Surgery 1987; 101: 746-52. Bangladesh J Pharmacol 2016; 11: 876-877 877