Ittiyavirah Sibi P, Ramalingam Kannan, Sathyan Arathy, Rajasree R S, Kuruniyan Mohamed Saheer, Quadri Syed Altafuddin, Elayadeth-Meethal Muhammed, Naseef Punnoth Poonkuzhi
Department of Pharmaceutical Sciences, Centre for Professional and Advanced Sciences, Cheruvandoor, Kottayam 686631, India.
College of Pharmaceutical Sciences, Government Thirumala Devaswom Medical College, Alappuzha 688005, India.
Saudi Pharm J. 2022 Dec;30(12):1781-1790. doi: 10.1016/j.jsps.2022.10.007. Epub 2022 Oct 19.
Inflammation-mediated alterations in glutamate neurotransmission constitute the most important pathway in the pathophysiology of various brain disorders. The excessive signalling of glutamate results in excitotoxicity, neuronal degeneration, and neuronal cell death. In the present study, we investigated the relative efficacy of black cumin () oil with high (5 % w/w) and low (2 % w/w) thymoquinone content (BCO-5 and BCO-2, respectively) in alleviating ibotenic acid-induced excitotoxicity and neuroinflammation in Wistar rats. It was found that BCO-5 reversed the abnormal behavioural patterns and the key inflammatory mediators (TNF-α and NF-κB) when treated at 5 mg/kg body weight. Immunohistochemical studies showed the potential of BCO-5 to attenuate the glutamate receptor subunits NMDA and GluR-2 along with increased glutamate decarboxylase levels in the brain tissues. Histopathological studies revealed the neuroprotection of BCO-5 against the inflammatory lesions, as evidenced by the normal cerebellum, astrocytes, and glial cells. BCO-2 on the other hand showed either a poor protective effect or no effect even at a 4-fold higher concentration of 20 mg/kg body weight indicating a very significant role of thymoquinone content on the neuroprotective effect of black cumin oil and its plausible clinical efficacy in counteracting the anxiety and stress-related neurological disorders under conditions such as depression and Alzheimer's disease.
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