Beneficial effect of omega-3 fatty acids supplementation on leaky gut, inflammation and oxidative stress in propionic acid-induced autism in aged rats.

IF 1.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Acta Pharmaceutica Pub Date : 2026-03-25 Print Date: 2026-03-01 DOI:10.2478/acph-2026-0008
Amal Aloud, Hayat Alzahrani, Shaista Arzoo, Raeesa Mohammed, Islam A Alredah, Alaa R Khatab
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引用次数: 0

Abstract

This study examined the effects of omega-3 fatty acids supplementation on gut barrier integrity, systemic inflammation, neurotrans-mission and oxidative stress, in an aged rat model of propionic acid (PPA)-induced neurotoxicity. Twenty-four aged male rats were divided into four groups: control, omega-3, PPA and PPA + omega-3. Serum cytokines, tight-junction proteins (TJP1), dopamine, serotonin, short-chain fatty acids (SCFAs), oxidative stress markers, and histopathology of the brain and small intestine were evaluated. PPA exposure significantly increased tumour necrosis factor-α (TNF-α) and interleukin-6 (IL-6) and reduced TJP1 expression, confirming gut barrier disruption and systemic inflammation. Omega-3 fatty acids supplementation selectively reduced IL-6 but did not reverse PPA-induced TNF-α elevation or oxidative stress. CLDN2 expression increased in PPA + omega-3 rats, suggesting a compensatory but incomplete barrier response. Dopamine, serotonin, and SCFA levels showed upward trends with supplementation but were not statistically significant. Histological analysis demonstrated partial preservation of neuronal and intestinal structure in the PPA + omega-3 group. Overall, omega-3 fatty acids exerted modest anti-inflammatory effects but failed to fully restore oxidative balance or barrier integrity in aged rats, suggesting that omega-3 fatty acids may be more effective as a preventive rather than restorative intervention in ageing-related gut-brain axis disruption.

补充omega-3脂肪酸对丙酸诱导的老年孤独症大鼠漏肠、炎症和氧化应激的有益影响。
本研究在丙酸(PPA)诱导的老年大鼠神经毒性模型中,研究了补充omega-3脂肪酸对肠道屏障完整性、全身炎症、神经传递和氧化应激的影响。24只老龄雄性大鼠分为4组:对照组、omega-3组、PPA组和PPA + omega-3组。评估血清细胞因子、紧密连接蛋白(TJP1)、多巴胺、血清素、短链脂肪酸(SCFAs)、氧化应激标志物以及脑和小肠的组织病理学。PPA暴露显著增加肿瘤坏死因子-α (TNF-α)和白细胞介素-6 (IL-6),降低TJP1表达,证实肠道屏障破坏和全身炎症。补充Omega-3脂肪酸可选择性地降低IL-6,但不能逆转ppa诱导的TNF-α升高或氧化应激。PPA + omega-3大鼠CLDN2表达增加,提示代偿性但不完全屏障反应。多巴胺、血清素和SCFA水平在补充后呈上升趋势,但没有统计学意义。组织学分析表明,PPA + omega-3组部分保存了神经元和肠道结构。总的来说,omega-3脂肪酸具有适度的抗炎作用,但不能完全恢复衰老大鼠的氧化平衡或屏障完整性,这表明omega-3脂肪酸可能更有效地预防而不是恢复与衰老相关的肠-脑轴破坏。
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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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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