Systemic and Lung Inflammation and Oxidative Stress Associated With Behavioral Changes Induced by Inhaled Paraquat Are Ameliorated by Carvacrol.

IF 3.5 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL PPAR Research Pub Date : 2024-08-24 eCollection Date: 2024-01-01 DOI:10.1155/2024/4049448
Arghavan Memarzia, Fatemeh Amin, Amin Mokhtari-Zaer, Zohre Arab, Saeideh Saadat, Mahrokh Heydari, Zahra Ghasemi, Farzaneh Naghdi, Mahmoud Hosseini, Mohammad Hossein Boskabady
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Abstract

Paraquat (PQ) is an herbicide toxin that induces injury in different organs. The anti-inflammatory and antioxidant effects of carvacrol were reported previously. The effects of carvacrol and pioglitazone (Pio) alone and their combination on inhaled PQ-induced systemic and lung oxidative stress and inflammation as well as behavioral changes were examined in rats. In this study, animals were exposed to saline (control [Ctrl]) or PQ (PQ groups) aerosols. PQ-exposed animals were treated with 0.03 mg/kg/day dexamethasone (Dexa), 20 and 80 mg/kg/day carvacrol (C-L and C-H), 5 mg/kg/day Pio, and Pio+C-L for 16 days. Inhaled PQ markedly enhanced total and differential white blood cell (WBC) counts, nitric oxide (NO), and malondialdehyde (MDA) levels but decreased catalase (CAT) and superoxide dismutase (SOD) activities and thiol levels both in the bronchoalveolar lavage fluid (BALF) and blood and increased interferon-gamma (INF-γ) and interleukin-10 (IL-10) levels in the BALF (p < 0.001 for all cases) except lymphocyte count in blood which was not significantly changed. The escape latency and traveled distance were increased in the PQ group. However, the time spent in the target quadrant in the Morris water maze (MWM) test and the duration of time latency in the dark room in the shuttle box test were reduced after receiving an electrical shock (p < 0.05-p < 0.001). Inhaled PQ-induced changes were significantly improved in carvacrol, Pio, Dexa, and especially in the combination of the Pio+C-L treated groups (p < 0.05-p < 0.001). Carvacrol and Pio improved PQ-induced changes similar to Dexa, but ameliorative effects produced by combination treatments of Pio+C-L were more prominent than Pio and C-L alone, suggesting a potentiating effect for the combination of the two agents.

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香芹酚可改善与吸入百草枯引起的行为改变有关的全身和肺部炎症及氧化应激反应
百草枯(PQ)是一种除草剂毒素,会对不同器官造成伤害。以前曾报道过香芹酚的抗炎和抗氧化作用。本研究以大鼠为研究对象,考察了香芹酚和吡格列酮单独使用或联合使用对吸入 PQ 引起的全身和肺部氧化应激、炎症以及行为变化的影响。在这项研究中,动物暴露于生理盐水(对照组 [Ctrl])或 PQ(PQ 组)气溶胶中。暴露于 PQ 的动物接受了 0.03 毫克/千克/天的地塞米松(Dexa)、20 和 80 毫克/千克/天的香芹酚(C-L 和 C-H)、5 毫克/千克/天的 Pio 和 Pio+C-L 的治疗,为期 16 天。吸入 PQ 显著提高了支气管肺泡灌洗液(BALF)和血液中白细胞(WBC)总数和差异数、一氧化氮(NO)和丙二醛(MDA)水平,但降低了过氧化氢酶(CAT)和超氧化物歧化酶(SOD)活性和硫醇水平,并提高了 BALF 中干扰素-γ(INF-γ)和白细胞介素-10(IL-10)水平(P < 0.001),但血液中的淋巴细胞计数变化不大。PQ 组的逃逸潜伏期和飞行距离均有所增加。然而,在接受电击后,莫里斯水迷宫(MWM)测试中目标象限的停留时间和穿梭箱测试中暗室潜伏时间均缩短(p < 0.05-p < 0.001)。吸入 PQ 引起的变化在香芹酚、Pio、Dexa,特别是在 Pio+C-L 组合治疗组中有明显改善(p < 0.05-p < 0.001)。香芹酚和 Pio 对 PQ 诱导的变化的改善程度与 Dexa 相似,但 Pio+C-L 联合治疗产生的改善效果比 Pio 和 C-L 单独治疗更明显,这表明两种药物的联合治疗具有增效作用。
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来源期刊
PPAR Research
PPAR Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.20
自引率
3.40%
发文量
17
审稿时长
12 months
期刊介绍: PPAR Research is a peer-reviewed, Open Access journal that publishes original research and review articles on advances in basic research focusing on mechanisms involved in the activation of peroxisome proliferator-activated receptors (PPARs), as well as their role in the regulation of cellular differentiation, development, energy homeostasis and metabolic function. The journal also welcomes preclinical and clinical trials of drugs that can modulate PPAR activity, with a view to treating chronic diseases and disorders such as dyslipidemia, diabetes, adipocyte differentiation, inflammation, cancer, lung diseases, neurodegenerative disorders, and obesity.
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Systemic and Lung Inflammation and Oxidative Stress Associated With Behavioral Changes Induced by Inhaled Paraquat Are Ameliorated by Carvacrol. Interaction between Nuclear Receptor and Alpha-Adrenergic Agonist Subtypes in Metabolism and Systemic Hemodynamics of Spontaneously Hypertensive Rats. Shared Mechanisms in Pparγ1sv and Pparγ2 Expression in 3T3-L1 Cells: Studies on Epigenetic and Positive Feedback Regulation of Pparγ during Adipogenesis. PPARG and the PTEN-PI3K/AKT Signaling Axis May Cofunction in Promoting Chemosensitivity in Hypopharyngeal Squamous Cell Carcinoma Peroxisome Proliferator-Activated Receptor γ Regulates Lipid Metabolism in Sheep Trophoblast Cells through mTOR Pathway-Mediated Autophagy
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