Nitrous Oxide Induces Prominent Cell Proliferation in Adult Rat Hippocampal Dentate Gyrus

The identification of distinct and more efficacious antidepressant treatments is highly needed. Nitrous oxide (N O) is an N-methyl-D-aspartic acid (NMDA) antagonist that has been reported to exhibit antidepressant effects in treatment-resistant depression (TRD) patients. Yet, no studies have investi...

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Veröffentlicht in:Frontiers in cellular neuroscience 2018-05, Vol.12, p.135-135
Hauptverfasser: Chamaa, Farah, Bahmad, Hisham F, Makkawi, Ahmad-Kareem, Chalhoub, Reda M, Al-Chaer, Elie D, Bikhazi, George B, Nahas, Ziad, Abou-Kheir, Wassim
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Sprache:eng
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Zusammenfassung:The identification of distinct and more efficacious antidepressant treatments is highly needed. Nitrous oxide (N O) is an N-methyl-D-aspartic acid (NMDA) antagonist that has been reported to exhibit antidepressant effects in treatment-resistant depression (TRD) patients. Yet, no studies have investigated the effects of sub-anesthetic dosages of N O on hippocampal cell proliferation and neurogenesis in adult brain rats. In our study, adult male Sprague-Dawley rats were exposed to single or multiple exposures to mixtures of 70% N O and 30% oxygen (O ). Sham groups were exposed to 30% O and the control groups to atmospheric air. Hippocampal cell proliferation was assessed by bromodeoxyuridine (BrdU) incorporation, and BrdU-positive cells were counted in the dentate gyrus (DG) using confocal microscopy. Results showed that while the rates of hippocampal cell proliferation were comparable between the N O and sham groups at day 1, levels increased by 1.4 folds at day 7 after one session exposure to N O. Multiple N O exposures significantly increased the rate of hippocampal cell proliferation to two folds. Therefore, sub-anesthetic doses of N O, similar to ketamine, increase hippocampal cell proliferation, suggesting that there will ultimately be an increase in neurogenesis. Future studies should investigate added N O exposures and their antidepressant behavioral correlates.
ISSN:1662-5102
1662-5102
DOI:10.3389/fncel.2018.00135