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Antidepressant-Like Effect of Ethanol in Mice Forced Swimming Test Is Mediated Via Inhibition of Nmda/Nitric Oxide/Cgmp Signaling Pathway Publisher Pubmed



Khan MI1, 2 ; Nikoui V3 ; Naveed A4 ; Mumtaz F5 ; Zaman H2 ; Haider A6 ; Aman W7 ; Wahab A2 ; Khan SN8 ; Ullah N9 ; Dehpour AR5, 10
Authors
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Authors Affiliations
  1. 1. Riphah Institute of Pharmaceutical Sciences, Riphah International University, G7-Islamabad, Pakistan
  2. 2. Department of Pharmacy, Kohat University of Science and Technology, Kohat, 26000, KPK, Pakistan
  3. 3. Razi Drug Research Center, Iran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Psychiatry, PIMS, Islamabad, Pakistan
  5. 5. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Department of Biological Sciences, National University of Medical Sciences, Rawalpindi, 46000, Punjab, Pakistan
  7. 7. Faculty of Pharmacy, University of Central Punjab, Lahore, Punjab, Pakistan
  8. 8. Department of Zoology, Kohat University of Science & Technology, Kohat, Pakistan
  9. 9. Institute of Basic Medical Sciences, Khyber Medical University, Peshawar, KPK, Pakistan
  10. 10. Brain and Spinal Cord Injury Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran

Source: Alcohol Published:2021


Abstract

There is evidence for a dramatic relationship between depression and alcohol consumption. Depressed patients may abuse ethanol because this agent reduces the symptoms of depression. In the current study, we aimed to investigate the NMDA/nitric oxide/cGMP pathway in the antidepressant-like effect of ethanol in an animal model of behavioral despair. Animals were subjected to locomotor activity in an open-field test separately, followed by a forced swimming test. During the forced swimming test (FST), ethanol (2 and 2.5 g/kg) significantly decreased the immobility time without altering the locomotor activity of animals. The antidepressant-like effect of ethanol (2.5 g/kg) was reversed by co-administration of N-methyl-D-aspartate (NMDA, 75 mg/kg), L-arginine (750 mg/kg), or sildenafil (5 mg/kg). In contrast, co-administration of MK-801 (0.05 mg/kg), ketamine (1 mg/kg), and ifenprodil (0.5 mg/kg) as antagonists of NMDAR, and NG-nitro-L-arginine methyl ester (L-NAME, 10 mg/kg), 7-nitroindazole (7-NI, 30 mg/kg), and methylene blue (10 mg/kg) as inhibitors of nitric oxide synthase (NOS), or 1H-[1,2,4]oxadiazole[4,3-a]quinoxalin-1-one (ODQ) (20 mg/kg), a nitric oxide/cyclic-guanosine monophosphate (NO-cGMP) inhibitor, with a subeffective dose of ethanol (1.5 g/kg), significantly decreased the immobility time in the FST. Furthermore, injection of ethanol 2.5 g/kg alone or 1.5 g/kg with a 7-NI subeffective dose, significantly decreased the nitrite levels in the hippocampus and prefrontal cortex. Hence, it is concluded that blockade of NMDA receptors and the nitric oxide/cyclic-guanosine monophosphate (NO-cGMP) pathway might be involved in the antidepressant-like effect of ethanol in mice. © 2021 Elsevier Inc.
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