Dose-dependent neuroprotective effect of caffeine on a rotenone-induced rat model of parkinsonism: A histological study

• Published in: Neuroscience letters Vol. 623; pp. 63 - 70
• Main Authors: Soliman, Amira M., Fathalla, Ahmed M., Moustafa, Ahmed A.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier B.V 03-06-2016
• Subjects: Animals; Brain - drug effects; Brain - pathology; Caffeine - pharmacology; Caffeine - therapeutic use; Dose-Response Relationship, Drug; Histological stains; Immunohistochemical; Male; Neurons - pathology; Neuroprotective Agents - pharmacology; Neuroprotective Agents - therapeutic use; Parkinson Disease - drug therapy; Parkinson Disease - etiology; Parkinson Disease - pathology; Parkinson’s disease; Pars Compacta - drug effects; Pars Compacta - pathology; Random Allocation; Rats; Rotenone; Rotenone model; Immunohistochemical; Rotenone model; Parkinson’s disease; Histological stains
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2016.04.057

•Rotenone produces Parkinsonism.•Caffeine is neuroprotective against Parkinsonism.•Caffeine hindered dopamine reduction in Parkinsonism rats.•A higher dose of caffeine was more effective against Parkinsonism.
Several lines of evidence have demonstrated an inverse relationship between caffeine utilization and Parkinson's disease (PD) progression. Caffeine is a methylxanthine known as a non-specific inhibitor of adenosine (A2A and A1) receptors in the cerebrum and demonstrated to be a neuroprotective medication. In this study, the neuroprotective efficacy of two different doses of caffeine ranging above the usual consumption dose and below the toxic dose was investigated using histopathological and immunohistochemical methods. Thirty-two male rats were randomly divided into 4 groups, with 8 in each group: vehicle control (1ml/kg/48h for 12 days), rotenone (1.5mg/kg/48h, s.c. for 12 days), low-dose Caffeine-treated: (10mg/kg IP. daily for 12 days), high-dose Caffeine-treated (20mg IP daily for 12 days). Twenty-four hours after the last rotenone injection, animals were sacrificed and brains were sectioned and prepared for histopathological staining with hematoxylinand eosin, cresyl violet and Mallory’s phosphotungestic acid haematoxylinand for immunohistochemical staining of tyrosine hydroxylase. Our study showed that the treatment with caffeine improved histopathological degeneration in the substantia nigra parts compacta (SNpc) neurons and hindered the reduction in dopamine concentration caused by rotenone. We also found that a higher dose of caffeine was more effective against histopathological degeneration. These results suggest that caffeine has a dose-dependent neuroprotective effect.