Savegnago Lucielli, Jesse Cristiano Ricardo, Pinto Larissa Garcia, Rocha Joao Batista Teixeira, Barancelli Daniela Aline, Nogueira Cristina Wayne, Zeni Gilson
Laboratório de Síntese, Reatividade e Avaliação Farmacológica e Toxicológica de Organocalcogênios, Centro de Ciências Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, CEP 97105-900, RS, Brazil.
Pharmacol Biochem Behav. 2008 Feb;88(4):418-26. doi: 10.1016/j.pbb.2007.09.015. Epub 2007 Sep 29.
This study investigated the possible antidepressant-like and anxiolytic-like effects of diphenyl diselenide, (PhSe)(2) in mice. The involvement of L-arginine-nitric oxide (NO)-cyclic guanosine monophosphate (cGMP) pathway in the antidepressant-like effect was also evaluated. The immobility times in the tail suspension test (TST) and forced swimming test (FST) were reduced by (PhSe)(2) (5-100 mg/kg; oral route, p.o.). The antiimmobility effect of (PhSe)(2) (5 mg/kg, p.o.) in the TST was prevented by pretreatment of mice with L-arginine [a substrate for nitric oxide synthase (NOS)], methylene blue [an inhibitor of NO synthase and sGC] and sildenafil [a phosphodiesterase 5 inhibitor]. Furthermore, a sub-effective dose of (PhSe)(2) (0.1 mg/kg, p.o.) produced a synergistic antidepressant-like effect with N(G)-nitro-L-arginine [L-NNA; 0.3mg/kg, i.p. inhibitor of NOS], (1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one [ODQ; 30 pmol/site i.c.v., a specific inhibitor of soluble guanylate cyclase (sGC)], fluoxetine and imipramine in the TST. (PhSe)(2) (50-100 mg/kg, p.o.) induced anxiolytic-like effect in the elevated plus-maze test and light/dark box. Together the results indicate that (PhSe)(2) elicited significant antidepressant-like and anxiolytic-like effects. The antidepressant-like action caused by (PhSe)(2) seems to involve an interaction with L-arginine-NO-cGMP pathway.
本研究调查了二苯基二硒醚((PhSe)₂)对小鼠可能的抗抑郁样和抗焦虑样作用。同时评估了L-精氨酸-一氧化氮(NO)-环磷酸鸟苷(cGMP)途径在抗抑郁样作用中的参与情况。在悬尾试验(TST)和强迫游泳试验(FST)中,(PhSe)₂(5 - 100 mg/kg;口服给药,p.o.)可减少不动时间。用L-精氨酸[一氧化氮合酶(NOS)的底物]、亚甲蓝[NO合酶和可溶性鸟苷酸环化酶(sGC)的抑制剂]和西地那非[磷酸二酯酶5抑制剂]预处理小鼠,可阻断(PhSe)₂(5 mg/kg,p.o.)在TST中的抗不动作用。此外,(PhSe)₂的亚有效剂量(0.1 mg/kg,p.o.)与N(G)-硝基-L-精氨酸[L-NNA;0.3mg/kg,腹腔注射,NOS抑制剂]、(1H-[1,2,4]恶二唑并[4,3-a]喹喔啉-1-酮[ODQ;30 pmol/位点,脑室内注射,可溶性鸟苷酸环化酶(sGC)的特异性抑制剂]、氟西汀和丙咪嗪在TST中产生协同抗抑郁样作用。(PhSe)₂(50 - 100 mg/kg,p.o.)在高架十字迷宫试验和明暗箱试验中诱导出抗焦虑样作用。这些结果共同表明,(PhSe)₂具有显著的抗抑郁样和抗焦虑样作用。(PhSe)₂引起的抗抑郁样作用似乎涉及与L-精氨酸-NO-cGMP途径的相互作用。