| ORIGINAL ARTICLE |
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| Year : 2018 | Volume
: 11
| Issue : 2 | Page : 123-130 |
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Syzygium aromaticum ethanol extract reduces AlCl3-induced neurotoxicity in mice brain through regulation of amyloid precursor protein and oxidative stress gene expression
Sanila Amber1, Syed Adnan Ali Shah2, Touqeer Ahmed1, Saadia Zahid1
1 Neurobiology Research Laboratory, Department of Healthcare Biotechnology, Atta-ur-Rahman School of Applied Biosciences, National University of Sciences and Technology, Islamabad, Pakistan
2 Atta-ur-Rahman Institute for Natural Product Discovery, (AuRIns), Universiti Teknologi MARA Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor D. E., ; Faculty of Pharmacy, Universiti Teknologi MARA Puncak Alam Campus, 42300 Bandar Puncak Alam, Selangor D. E, Malaysia
Correspondence Address:
Saadia Zahid
Neurobiology Research Laboratory, Department of Healthcare Biotechnology, Atta-ur-Rahman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad
Pakistan
 Source of Support: None, Conflict of Interest: None  | 1 |
DOI: 10.4103/1995-7645.225019
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Objective: To investigate the neuroprotective effects of Syzygium aromaticum (S. aromaticum) extract (500 mg/kg) on AlCl3 (300 mg/kg)-induced mouse model of oxidative stress and neurotoxicity. Methods: An ethanolic extract of S. aromaticum seeds was prepared and the active compounds were identified using nuclear magnetic resonance spectroscopy. BALB/ c mice were divided into five groups (negative control, AlCl3-treated, self-recovery, AlCl3 + S. aromaticum, S. aromaticum only; n=10) and treated with AlCl3 and S. aromaticum extract. Expression of oxidative markers [Superoxide dismutase 1 (SOD1) and peroxiredoxin 6 (Prdx6)] and amyloid precursor protein (APP) in the hippocampus and cortex was evaluated via PCR. Histopathological assessment was performed to investigate the extent of neurodegeneration. Results: It was observed that AlCl3 exposure increased the expression of APP770 while simultaneously down regulated the expression of APP695. AlCl3 also induced a significant decrease (P<0.05) and an increase (P<0.05) in the expression level of SOD1 and Prdx6, respectively. A substantial decrease substantial (P<0.05) in the density of Nissl substance was also observed in cortex of the mice treated with AlCl3. Interestingly, treatment with S. aromaticum extract normalized the alterations in the expression level of SOD1, Prdx6 and APP isoforms and improved the neuronal structural damage. Conclusions: The results showed that S. aromaticum is a promising antioxidant and a neuroprotective agent.
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