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Inducible Nitric Oxide Synthase Inhibition in the Medial Prefrontal Cortex Attenuates the Anxiogenic-Like Effect of Acute Restraint Stress via CB1 Receptors

Bibliographic Data

ID15526220
AuthorsArthur Alves Coelho (0000-0001-6174-0780, Universidade de São Paulo), Carla Vila-Verde (Universidade de São Paulo), Ariandra Guerini Sartim (0000-0001-6383-4262, Universidade de São Paulo), Daniela L Uliana (0000-0002-7354-7176, Universidade de São Paulo), Laura A Braga (Universidade de São Paulo), Francisco Silveira Guimarães (0000-0003-4092-7778, Universidade de São Paulo), Sabrina Francesca Lisboa (0000-0002-2069-3524, Universidade de São Paulo, corresponding author)
Year2022
Volume13
Pages923177-923177
Publication date2022-07-14
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2022.923177
PMID35911236
OpenAlexW4285389872
LanguageEN
Citations received1
References cited88

Stress exposure can result in several proinflammatory alterations in the brain, including overexpression of the inducible isoform of nitric oxide synthase (iNOS) in the medial prefrontal cortex (mPFC). These changes may be involved in the development of many psychiatric conditions. However, it is unknown if iNOS in mPFC plays a significant role in stress-induced behavioral changes. The endocannabinoid (ECB) system is also influenced by stress. Its activation seems to be a counter regulatory mechanism to prevent or decrease the stress-mediated neuroinflammatory consequences. However, it is unclear if the ECB system and iNOS interact to influence stress consequences. This study aimed to test the hypothesis that the anti-stress effect of iNOS inhibition in mPFC involves the local ECB system, particularly the CB 1 cannabinoid receptors. Male Wistar rats with guide cannula aimed at the mPFC were submitted to acute restraint stress (RS) for 2 h. In the following morning, rats received bilateral microinjections of vehicle, AM251 (CB 1 antagonist; 100 pmol), and/or 1400W (iNOS selective inhibitor; 10 -4 , 10 -3 , or 10 -2 nmol) into the prelimbic area of mPFC (PL-mPFC) before being tested in the elevated plus-maze (EPM). iNOS inhibition by 1400W prevented the anxiogenic-like effect observed in animals submitted to RS. The drug did not promote behavior changes in naive animals, demonstrating a stress-dependent effect. The 1400W-anti-stress effect was prevented by local pretreatment with AM251. Our data suggest that iNOS inhibition may facilitate the local endocannabinoid signaling, attenuating stress effects

AM251 · Antagonist · Anxiety · Anxiogenic · Anxiolytic · Basolateral amygdala · Cannabinoid · Cannabinoid receptor · Elevated plus maze · Endocannabinoid system · Infralimbic cortex · Nitric oxide · Nitric oxide synthase · Prefrontal cortex · Receptor · Cannabis and Cannabinoid Research · Chemistry · Medicine · Neuroscience · Psychology · Stress Responses and Cortisol · Tryptophan and brain disorders · Endocrinology · Internal Medicine · Pharmacology

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Citations per year0.33
Citation span2023 - 2023 (1)
Highly citedNo

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