PMID- 34592305 OWN - NLM STAT- MEDLINE DCOM- 20220204 LR - 20220204 IS - 1879-0712 (Electronic) IS - 0014-2999 (Linking) VI - 911 DP - 2021 Nov 15 TI - Ameliorative effect of myrcene in mouse model of Alzheimer's disease. PG - 174529 LID - S0014-2999(21)00685-3 [pii] LID - 10.1016/j.ejphar.2021.174529 [doi] AB - Myrcene (Myr) has been reported to show neuroprotective effects in cerebral ischemia. In this research work, we investigated the Myr effect on neurobehavioural, and neuropathological alteration in mice induced by Aluminium trichloride (AlCl(3)) and D - galactose. The administration of AlCl(3) (5 mg/kg; p. o.), and D - galactose (60 mg/kg; i. p.) for 90 days in mice resulted in spatial learning and memory deficits, cognitive decline, as well as neurotoxicity. The treatments with Myr low dose (100 mg/kg), Myr high dose (200 mg/kg), donepezil (2 mg/kg), and Myr low dose + donepezil (100 + 2 mg/kg) were administered via intraperitoneal route for 30 days significantly reversed the neurobehavioral, and neuropathological effects of AlCl(3) and D - galactose in mice. The results of behavioural tests such as Morris water maze, elevated plus maze, and locomotor; biochemical analysis such as malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD), catalase (CAT), nitrite, and acetylcholinesterase (AChE); and ELISA tests such as mouse beta - secretase (BACE), amyloid-beta peptide(1-42) (Abeta(1 - 42)), tumor necrosis factor - alpha (TNF-alpha), interleukin - 6 (IL-6), and brain-derived neurotrophic factor (BDNF) demonstrated a significant (p < 0.05) neuroprotective effect of the Myr and donepezil co-treatments. In addition, hematoxylin and eosin staining of the cerebral cortex and hippocampus revealed eosinophilic lesions and hyperchromatic nuclei in Alzheimer's disease mice, but treatments with Myr low dose, Myr high dose, donepezil, and Myr low dose + donepezil reversed these neurodegenerative effects. Myr showed these activities by enhancing synaptic plasticity and cholinergic activity, as well as reducing oxidative damage, neuroinflammation, Abeta(1-42) aggregations, and histopathological damage. Myr alone and in combination with donepezil may serve as a potential candidate for the treatment of Alzheimer's disease. CI - Copyright (c) 2021 Elsevier B.V. All rights reserved. FAU - Kumar, Rakesh AU - Kumar R AD - School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, 144411, Punjab, India. FAU - Kumar, Rajan AU - Kumar R AD - School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, 144411, Punjab, India. FAU - Sharma, Neha AU - Sharma N AD - School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, 144411, Punjab, India. FAU - Khurana, Navneet AU - Khurana N AD - School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, 144411, Punjab, India. Electronic address: navi.pharmacist@gmail.com. LA - eng PT - Journal Article DEP - 20210928 PL - Netherlands TA - Eur J Pharmacol JT - European journal of pharmacology JID - 1254354 SB - IM MH - *Alzheimer Disease OTO - NOTNLM OT - Aluminium trichloride OT - Alzheimer's disease OT - D - galactose OT - Donepezil OT - Myrcene OT - Oxidative stress EDAT- 2021/10/01 06:00 MHDA- 2022/02/05 06:00 CRDT- 2021/09/30 20:14 PHST- 2021/04/22 00:00 [received] PHST- 2021/09/23 00:00 [revised] PHST- 2021/09/24 00:00 [accepted] PHST- 2021/10/01 06:00 [pubmed] PHST- 2022/02/05 06:00 [medline] PHST- 2021/09/30 20:14 [entrez] AID - S0014-2999(21)00685-3 [pii] AID - 10.1016/j.ejphar.2021.174529 [doi] PST - ppublish SO - Eur J Pharmacol. 2021 Nov 15;911:174529. doi: 10.1016/j.ejphar.2021.174529. Epub 2021 Sep 28.