Effects of alpha-pinene on depressive behaviors in a dextromethorphan-induced depression model in rats

IF 2.7 Q2 MEDICINE, GENERAL & INTERNAL
Danial Hasanisadr DVM , Kaveh Rahimi PhD , Zohreh Ghotbeddin PhD
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引用次数: 0

Abstract

Background

Depression, a multifactorial psychiatric disorder, affects millions of people worldwide and has limited effective therapeutic options. This study was aimed at investigating the potential antidepressant effects of alpha-pinene (aPI) in a dextromethorphan (DEX)-induced pharmacological model in rats.

Methods

Thirty-two adult male Wistar rats were randomly assigned to four groups (n = 8). The control group received the vehicle (DMSO diluted in saline, 0.5 mL/kg, IP) for 14 days. The model group was administered DEX (40 mg/kg, IP) for 14 days to induce neurobehavioral alterations associated with depressive-like states. Two treatment groups received alpha-pinene (5 or 10 mg/kg, IP), which was dissolved in DMSO diluted in saline and administered 30 min before DEX injection for 14 days. Behavioral assessments, including the sucrose preference test, tail suspension test, and forced swimming test, were conducted to evaluate depressive-like behaviors. Hippocampal levels of TNF-α and MDA were measured with ELISA to assess neuroinflammation and oxidative stress.

Results

DEX administration resulted in significant depressive-like behaviors, as evidenced by increased immobility in the forced swimming test and tail suspension test, and decreased sucrose preference (P < 0.001). Treatment with alpha-pinene (5 and 10 mg/kg) significantly ameliorated these behavioral alterations (P < 0.05), and no significant difference was observed between doses. Additionally, DEX significantly elevated hippocampal TNF-α and MDA levels, whereas alpha-pinene treatment markedly decreased these levels (P < 0.05).

Conclusion

These findings suggest that alpha-pinene exerts antidepressant-like effects in a DEX-induced pharmacological model, potentially through modulation of neuroinflammatory and oxidative stress pathways. Nevertheless, confirmation in well-validated animal models of depression is required to strengthen the translational relevance of these findings.
α -蒎烯对右美沙芬抑郁模型大鼠抑郁行为的影响
抑郁症是一种多因素精神障碍,影响着全世界数百万人,但有效的治疗选择有限。本研究旨在探讨α -蒎烯(aPI)在右美沙芬(DEX)诱导的大鼠药理模型中的潜在抗抑郁作用。方法32只成年雄性Wistar大鼠随机分为4组(n = 8)。对照组给药(DMSO用生理盐水稀释,0.5 mL/kg, IP) 14 d。模型组大鼠连续14 d给予DEX (40 mg/kg, IP)诱导抑郁样状态相关的神经行为改变。两组均给予α -蒎烯(5或10 mg/kg, IP),溶解于用生理盐水稀释的DMSO中,在注射DEX前30 min给药,连续14 d。行为评估包括蔗糖偏好测试、悬尾测试和强迫游泳测试,以评估抑郁样行为。ELISA法检测海马组织TNF-α和MDA水平,评估神经炎症和氧化应激。结果在强迫游泳试验和悬尾试验中,大鼠的不动能力增加,对蔗糖的偏好降低(P < 0.001),表明给药后大鼠出现了明显的抑郁样行为。用α -蒎烯(5和10 mg/kg)治疗可显著改善这些行为改变(P < 0.05),不同剂量间无显著差异。此外,DEX显著提高海马TNF-α和MDA水平,而α -蒎烯治疗显著降低这些水平(P < 0.05)。结论在dex诱导的药理学模型中,α -蒎烯可能通过调节神经炎症和氧化应激途径发挥抗抑郁样作用。然而,需要在经过充分验证的抑郁症动物模型中进行确认,以加强这些发现的转化相关性。
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来源期刊
Journal of Taibah University Medical Sciences
Journal of Taibah University Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
3.40
自引率
4.50%
发文量
130
审稿时长
29 days
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