Department of Cellular and Molecular Sciences, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Herbal Pharmacology Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Sep;397(9):6879-6888. doi: 10.1007/s00210-024-03069-9. Epub 2024 Apr 3.
Selective serotonin reuptake inhibitors (SSRIs) are widely used drugs for the treatment of depression. Citalopram is one of the most prescribed SSRIs that is useful for the treatment of depression, obsessive-compulsive disorder, and anxiety disorders. On the other hand, crocin (active constitute of saffron) has pro-cognitive and mood enhancer effects. Also, both citalopram and crocin affect the function and expression of brain-derived neurotrophic factor (BDNF) and synaptophysin, two molecular factors that are involved in cognitive functions and mood. In the present study, we aim to investigate the interaction effect of citalopram and crocin on rats' performance in the open field test (locomotor activity and anxiety-like behavior) and the shuttle box (passive avoidance memory). Citalopram was injected at the doses of 10, 30, and 50 mg/kg, and crocin was injected at the dose of 50 mg/kg; all administrations were intraperitoneal. Real-time PCR was used to assess the expression level of BDNF and synaptophysin in the hippocampus. The results showed that citalopram (30 and 50 mg/kg) impaired passive avoidance memory and decreased BDNF and synaptophysin expression in the hippocampus, while crocin reversed memory impairment, and BDNF and synaptophysin expression in the hippocampus of rats received citalopram 30 mg/kg. Also, crocin partially showed these effects in rats that received citalopram 50 mg/kg. The results of the open field test were unchanged. In conclusion, we suggested that BDNF and synaptophysin may be involved in the effects of both citalopram and crocin.
选择性 5-羟色胺再摄取抑制剂(SSRIs)被广泛用于治疗抑郁症。西酞普兰是最常被开处方的 SSRIs 之一,可有效治疗抑郁症、强迫症和焦虑症。另一方面,西红花苷(藏红花的活性成分)具有促进认知和改善情绪的作用。此外,西酞普兰和西红花苷都会影响脑源性神经营养因子(BDNF)和突触小泡蛋白的功能和表达,这两种分子因素都参与认知功能和情绪。在本研究中,我们旨在研究西酞普兰和西红花苷对大鼠在旷场试验(运动活性和焦虑样行为)和穿梭箱(被动回避记忆)中的作用的交互效应。西酞普兰的注射剂量为 10、30 和 50mg/kg,西红花苷的注射剂量为 50mg/kg;所有给药途径均为腹腔注射。实时 PCR 用于评估海马中 BDNF 和突触小泡蛋白的表达水平。结果表明,西酞普兰(30 和 50mg/kg)损害了被动回避记忆,并降低了海马中 BDNF 和突触小泡蛋白的表达,而西红花苷逆转了西酞普兰 30mg/kg 处理大鼠的记忆损伤,并恢复了海马中 BDNF 和突触小泡蛋白的表达。此外,西红花苷在接受西酞普兰 50mg/kg 处理的大鼠中部分表现出这些作用。旷场试验的结果没有改变。总之,我们认为 BDNF 和突触小泡蛋白可能参与了西酞普兰和西红花苷的作用。