Investigation of the effects of hydroxychloroquine on rats with pulmonary contusion caused by blunt thoracic trauma.

IF 1.3
Acta cirurgica brasileira Pub Date : 2026-08-14 eCollection Date: 2026-01-01 DOI:10.1590/acb415026
Ali İhsan Anadolulu, Sinem Aydöner, Ahmet Pirim, Seyma Ozkanli, Çiğdem Ulukaya Durakbaşa
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Abstract

Purpose: To investigate the early and late effects of hydroxychloroquine (HCQ) on inflammation, fibrosis, and apoptosis in an experimental rat model of pulmonary contusion.

Methods: Thirty-five male Wistar albino rats were randomly allocated into five groups (n = 7): control, pulmonary contusion evaluated on day 3 or day 10 (PC-3 and PC-10), and pulmonary contusion treated with HCQ at 100 mg/kg/day by gavage and evaluated on day 3 or day 10 (PCHCQ-3 and PCHCQ-10). Lung injury was assessed histopathologically by alveolar edema, congestion, leukocyte infiltration, and fibrosis scores and immunohistochemically by caspase-3, inducible nitric oxide synthase (iNOS), and endothelial nitric oxide synthase (eNOS) expression.

Results: No alveolar edema was observed. Congestion and leukocyte infiltration were significantly greater in all contusion groups than in the control group. Fibrotic changes were detected on day 10 in both treated and untreated contusion groups. Caspase-3 and iNOS expression were significantly higher in the contusion groups than in the control group. HCQ did not significantly reduce leukocyte infiltration, fibrosis, apoptosis, or iNOS expression compared with the corresponding untreated groups.

Conclusion: HCQ administered at 100 mg/kg/day for three or 10 days did not demonstrate significant anti-inflammatory, anti-apoptotic, or antifibrotic effects in this rat model of pulmonary contusion.

羟基氯喹对钝性胸外伤大鼠肺挫伤的影响。
目的:探讨羟基氯喹(HCQ)对实验性肺挫伤大鼠模型炎症、纤维化和细胞凋亡的早期和晚期影响。方法:雄性Wistar白化大鼠35只,随机分为5组(n = 7):对照组,于第3天或第10天评估肺挫伤(PC-3和PC-10); HCQ以100 mg/kg/d灌胃治疗肺挫伤,于第3天或第10天评估(PCHCQ-3和PCHCQ-10)。肺损伤通过肺泡水肿、充血、白细胞浸润和纤维化评分进行组织病理学评估,通过caspase-3、诱导型一氧化氮合酶(iNOS)和内皮型一氧化氮合酶(eNOS)表达进行免疫组织化学评估。结果:未见肺泡水肿。各挫伤组的充血和白细胞浸润均明显高于对照组。治疗组和未治疗组均在第10天检测到纤维化改变。挫伤组Caspase-3、iNOS表达明显高于对照组。与相应的未处理组相比,HCQ没有显著降低白细胞浸润、纤维化、凋亡或iNOS表达。结论:HCQ给药剂量为100 mg/kg/天,连续3天或10天,对肺挫伤大鼠模型均无明显的抗炎、抗凋亡或抗纤维化作用。
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