Comparing the Efficacy of Escitalopram with and without Crocin in Restoring I/O Functions and LTP within the Hippocampal CA1 Region of Stressed Rats.

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Advanced biomedical research Pub Date : 2024-11-30 eCollection Date: 2024-01-01 DOI:10.4103/abr.abr_18_24
Mehran Joodaki, Maryam Radahmadi, Hojjatallah Alaei
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Abstract

Background: Escitalopram, a pharmacological compound, and crocin, the active compound of saffron, influence brain functions and serotonin levels. This study examined the efficacy of escitalopram with and without crocin in restoring the input-output (I/O) functions and long-term potentiation (LTP) within the hippocampal cornu ammonis 1 (CA1) region of stressed rats.

Materials and methods: Rats were divided into six groups: control (Co), sham (Sh), stress-recovery (St-Rec), stress-escitalopram (St-Esc), stress-crocin (St-Cr), and stress-escitalopram-crocin (St-Esc-Cr) groups. They underwent 14 days of restraint stress (6 h/day). After being subjected to stress, they received 14 days of escitalopram (20 mg/kg) and crocin (30 mg/kg), as well as co-administration of these two compounds during the next 14 days. The field excitatory postsynaptic potential (fEPSP) slope and amplitude were measured using I/O functions and LTP induction in the CA1 region. Corticosterone (CORT) levels were also evaluated.

Results: The fEPSPs slope and amplitude in the I/O functions and LTP induction significantly decreased in stressed rats without therapeutic intervention. These variables in the I/O functions declined in rats with escitalopram administration alone. All electrophysiological parameters showed an increase in rats treated with crocin alone compared to stressed subjects without any treatment. Serum CORT levels decreased only with crocin treatment for stressed rats.

Conclusion: Neural excitability and memory within the CA1 region were severely disrupted among stressed rats without any treatment. Furthermore, administering crocin alone improved neural excitability and memory post-chronic stress. Treatment with escitalopram alone also impaired neural excitability within the CA1 region. The use of escitalopram with and without crocin did not enhance memory under chronic stress.

比较艾司西酞普兰加与不加藏红花素对应激大鼠海马CA1区I/O功能和LTP的恢复作用。
背景:药物化合物艾司西酞普兰和藏红花的活性化合物藏红花素影响脑功能和血清素水平。本研究考察了艾司西酞普兰加藏红花素和不加藏红花素对应激大鼠海马角氨1 (CA1)区输入输出(I/O)功能和长期增强(LTP)功能的恢复作用。材料与方法:将大鼠分为6组:对照组(Co)、假手术组(Sh)、应激恢复组(St-Rec)、应激-艾赛西酞普兰组(St-Esc)、应激-藏红花素组(St-Cr)和应激-艾赛西酞普兰-藏红花素组(St-Esc- cr)。施加约束应激(6 h/d) 14 d。应激后,给予14天艾司西酞普兰(20 mg/kg)和藏红花素(30 mg/kg),并在接下来的14天内共同给予这两种化合物。利用I/O函数和CA1区LTP诱导,测量了场兴奋性突触后电位(fEPSP)的斜率和振幅。皮质酮(CORT)水平也被评估。结果:应激大鼠I/O功能和LTP诱导中fEPSPs的斜率和振幅显著降低。在单独给药艾司西酞普兰的大鼠中,这些变量的I/O功能下降。所有电生理参数显示,与没有任何治疗的应激组相比,单独服用藏红花素的大鼠的电生理参数有所增加。应激大鼠血清CORT水平仅在藏红花素治疗下降低。结论:应激大鼠CA1区神经兴奋性和记忆功能受到严重破坏。此外,单独施用藏红花素可改善慢性应激后的神经兴奋性和记忆。单独使用艾司西酞普兰治疗也会损害CA1区的神经兴奋性。使用艾司西酞普兰加或不加藏红花素对慢性应激下的记忆没有增强作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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