Mostofa Jamal

ORCID: 0000-0002-2275-3797
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About
Contact & Profiles
Research Areas
  • Neuroscience and Neuropharmacology Research
  • Neurotransmitter Receptor Influence on Behavior
  • Poisoning and overdose treatments
  • Restraint-Related Deaths
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Nicotinic Acetylcholine Receptors Study
  • Memory and Neural Mechanisms
  • Pharmacological Effects and Toxicity Studies
  • Adipose Tissue and Metabolism
  • Injury Epidemiology and Prevention
  • Cannabis and Cannabinoid Research
  • Cholinesterase and Neurodegenerative Diseases
  • Neurogenesis and neuroplasticity mechanisms
  • Epilepsy research and treatment
  • Nerve injury and regeneration
  • Autopsy Techniques and Outcomes
  • Pharmacogenetics and Drug Metabolism
  • Birth, Development, and Health
  • Alcoholism and Thiamine Deficiency
  • Neonatal Health and Biochemistry
  • Burn Injury Management and Outcomes
  • Heme Oxygenase-1 and Carbon Monoxide
  • Neuroscience of respiration and sleep
  • Pharmacology and Obesity Treatment
  • Drug-Induced Hepatotoxicity and Protection

Kagawa University
2015-2025

Zahedan University of Medical Sciences
2025

Baghdad Medical City
2024

Ministry of Health
2024

Mohammed Bin Rashid University of Medicine and Health Sciences
2024

University of New England
2021

Tokyo Medical Examiner's Office
2007

Salsolinol, a neuropharmacologically active compound, is formed by the condensation of acetaldehyde (AcH) with dopamine (DA) in brain. The aim our study was to examine effect high concentration AcH on salsolinol formation and compare release DA, serotonin (5-HT), striatum nucleus accumbens (NAc) free-moving rats.After insertion microdialysis probe, male Wistar rats (250-300 g) were treated cyanamide (CY, potent aldehyde dehydrogenase inhibitor) + ethanol (EtOH), CY 4-methylpyrazole (4-MP,...

10.1097/01.alc.0000078617.33026.ad article EN Alcoholism Clinical and Experimental Research 2003-08-01

The in vivo formation of salsolinol (1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquionoline), an endogeneous condensation product dopamine (DA) with acetaldehyde (AcH), was examined following the administration cyanamide (CY) plus ethanol (EtOH) using microdialysis-high-performance liquid chromatography electrochemical detection.After insertion a microdialysis probe into striatum, rats were treated CY (a potent inhibitor aldehyde dehydrogenase, 50 mg/kg), 4-methylpyrazole (4-MP, strong...

10.1093/alcalc/agg056 article EN Alcohol and Alcoholism 2003-04-24
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