Personal Information
- Pharmacology and toxicology
- Neuropharmacology
- Preclinical drug discovery
- Cellular and molecular biology
- Neurological disorders
- Huntington’s Disease
- Parkinson’s Disease
- M.Pharm. Semester I
- MPL101T Modern Pharmaceutical Analytical Techniques
- MPL102T Advanced Pharmacology -I
- MPL103T Pharmacological and Toxicological Screening Methods - I
- MPL104T Cellular and Molecular Pharmacology
- MPL05P Pharmacology Practical -I
- MPL106S Seminar/Assignment
Research
- Senior Research Fellowship (SRF) awarded by Indian Council of Medical Research (ICMR), for the project entitled “Neuropharmacological investigation on raloxifene and fulvestrant against haloperidol-induced animal model of Tardive Dyskinesia: Possible role of GPR30 receptor”
Animal Model Validated & Developed
- Haloperidol-Induced Tardive Dyskinesia model in Adult Wistar Rats and in Zebrafish
- 3-Nitropropionic acid (3-NP) induced Huntington’s disease in adult zebrafish.
- Mercury-Induced Amyotrophic Lateral Sclerosis in Adult Wistar Rats
- Ethidium Bromide Induced Multiple Sclerosis Model in Adult Wistar Rats
Target explored in neurological disorders
GPER1/GPR30, PI3k/Akt, Nrf2/HO-1, GSK-3β, c-JNK/p38MAPK
Drug Induced Movement Disorder
- Raloxifene and Fulvestrant Exert Antioxidant, Anti-Inflammatory, and Antiapoptotic Action Against Haloperidol-Induced Tardive Dyskinesia in Rats via Activation of the GPER1/PI3k/Akt/Nrf2/HO-1 Signaling Pathways. Journal of biochemical and molecular toxicology, 39(8), e70413.
- G-Protein-Coupled Estrogen Receptor 1 (GPER1) Activation Mitigates Haloperidol-Induced Neurotoxicity in SHSY-5Y Cells and Improves Motor Functions in Adult Zebrafish. Neurochemical research, 50(2), 119.
- Glycyrrhizic Acid Mitigates Haloperidol-Induced Neurotoxicity in SHSY-5Y Cells and Rats Via Activation of PI3k/Akt/Nrf2 Pathways. Neurochemical Research, 50(1), 1-19.
- Bacillus Calmette–Guérin Vaccine Attenuates Haloperidol-Induced TD-like Behavioral and Neurochemical Alteration in Experimental Rats." Biomolecules 13, no. 11 (2023): 1667.
Huntington’s Disease and Parkinson’s Disease
- Auranofin-loaded chitosan-lipid hybrid nanoparticle protects against the in-vitro/in-vivo model of Parkinson’s disease via modulation of GSK-3β/Nrf2/HO-1 signaling. European Journal of Pharmacology, 177523.
- Elucidating the neuroprotective potential of arbutin in 3-NPA induced HD-like pathology: Insights from in silico, in vitro, and in vivo models. Behavioural Brain Research, 483, 115475.
Multiple Sclerosis
- Nrf2/HO-1 Signaling Stimulation through Acetyl-11-Keto-Beta-Boswellic Acid (AKBA) Provides Neuroprotection in Ethidium Bromide-Induced Experimental Model of Multiple Sclerosis." Genes 13, no. 8 (2022): 1324
- Neuroprotection by solanesol against ethidium bromide-induced multiple sclerosis-like neurobehavioral, molecular, and neurochemical alterations in experimental rats, Phytomedicine Plus, Volume 1, Issue 4, 2021,100051
- Inhibition of c-JNK/p38MAPK signaling pathway by Apigenin prevents neurobehavioral and neurochemical defects in ethidium bromide-induced experimental model of multiple sclerosis in rats: Evidence from CSF, blood plasma and brain samples. Phytomedicine Plus 1, no. 4 (2021): 100139.
Alzheimer’s Disease
- In vitro and in vivo investigations of chromone derivatives as potential multitarget-directed ligands: Cognitive amelioration utilizing a scopolamine-induced zebrafish model. ACS Chemical Neuroscience, 15(14), 2565-2585.
- ML-based prediction to experimental validation: Development of dihydroquinazoline based multi-potent ligands as anti-Alzheimer's agents. Computers in Biology and Medicine, 196, 110762.
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