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DOI 10.1097/fbp.0000000000000784

Медицинская библиотека · Behavioural pharmacology · 2024

Antidepressive synergism between crocin and D-AP5 in acute restraint-stressed mice.

Gerami Sana-Sadat, Ebrahimi-Ghiri Mohaddeseh, Khakpai Fatemeh, Zarrindast Mohammad-Reza

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Аннотация

Emerging evidence suggests that crocin rescues stress-induced depressive symptoms in mice via stimulation of hippocampal neurogenesis. Glutamate modulators mainly involving N-methyl- d -aspartate (NMDA) receptors (NMDARs) have highlighted a role in neural development, synaptic plasticity, and depression. The research presented here was designed to appraise the interaction between NMDAR agents and crocin on depressive-related behaviors in the NMRI male mice exposed to acute restraint stress (ARS) for a period of 4 h. The mice were submitted to the splash test, forced swimming test, and tail suspension test to evaluate depressive-like behavior. The ARS decreased the grooming duration in the splash test and increased immobility time in the forced swimming test and tail suspension test, suggesting a depressive-like phenotype. NMDA (0.25 and 0.5 μg/mouse, intracerebroventricular) did not alter depression-related profiles in both non-acute restraint stress (NARS) and ARS mice, while the same doses of NMDAR antagonist D-AP5 potentiated the antidepressive-like activities in the ARS mice compared with the NARS mice. Moreover, a low dose of NMDA did not change depression-related parameters in the crocin-treated NARS or ARS mice, while D-AP5 enhanced the crocin response in the NARS and ARS mice. Isobologram analysis noted a synergism between crocin and D-AP5 on antidepressive-like behavior in the NARS and ARS mice. Collectively, the combination of crocin and D-AP5 was shown to mitigate depression symptoms and can be potentially used for the treatment of depression disorders.

Для цитирования: Gerami Sana-Sadat, Ebrahimi-Ghiri Mohaddeseh, Khakpai Fatemeh, Zarrindast Mohammad-Reza. Antidepressive synergism between crocin and D-AP5 in acute restraint-stressed mice.. Behavioural pharmacology. 2024. DOI: 10.1097/fbp.0000000000000784.

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