Department of Morphological Sciences, Universidade Estadual de Maringá, 87020-900, Maringá, Brazil.
Department of Experimental Pathology, Universidade Estadual de Londrina, 86057-970, Londrina, Brazil.
Neurotoxicology. 2020 Mar;77:193-204. doi: 10.1016/j.neuro.2020.01.011. Epub 2020 Jan 30.
Given the well-known antioxidant and neuroprotective properties of quercetin, the aim of this work was to evaluate the effects of quercetin stabilized by microencapsulation at two doses (10 mg kg and 100 mg kg) on the oxidative/antioxidant status, number and morphological features of ICC, nitrergic neurons and M2-like macrophages in jejunum of diabetic rats. The rats were randomly distributed into six groups: normoglycemic control (N), diabetic control (D) and either normoglycemic or diabetic groups treated with quercetin-loaded microcapsules at a dose of 10 mg kg (NQ10 and DQ10, respectively) or 100 mg kg (NQ100 and DQ100, respectively). After 60 days, the jejunum was collected. Whole mounts were immunostained for Ano1, nNOS and CD206, and oxidative stress levels and total antioxidant capacity of the jejunum were measured. Diabetes led to a loss of ICC and nitrergic neurons, but increased numbers of M2-like macrophages and elevated levels of oxidative stress were seen in diabetic animals. High-dose administration of quercetin (100 mg kg) further aggravated the diabetic condition (DQ100) but this treatment resulted in harmful effects on healthy rats (NQ100), pointing to a pro-oxidant activity. However, low-dose administration of quercetin (10 mg kg) gave rise to antioxidant and protective effects on ICC, nNOS, macrophages and oxidative/antioxidant status in DQ100, but NQ100 displayed infrequent negative outcomes in normoglycemic animals. Microencapsulation of the quercetin may become promising alternatives to reduce diabetes-induced oxidative stress but antioxidant therapies should be careful used under healthy status to avoid toxic effects.
鉴于槲皮素具有抗氧化和神经保护的特性,本研究旨在评估微囊化槲皮素(剂量为 10mg/kg 和 100mg/kg)对糖尿病大鼠空肠氧化/抗氧化状态、ICC 数量和形态特征、氮能神经元和 M2 样巨噬细胞的影响。将大鼠随机分为六组:正常血糖对照组(N)、糖尿病对照组(D)和分别用 10mg/kg(NQ10 和 DQ10)或 100mg/kg(NQ100 和 DQ100)载有槲皮素的微囊处理的正常血糖或糖尿病组。60 天后,收集空肠。对 Ano1、nNOS 和 CD206 进行全组织免疫染色,并测量空肠的氧化应激水平和总抗氧化能力。糖尿病导致 ICC 和氮能神经元丧失,但糖尿病动物的 M2 样巨噬细胞数量增加,氧化应激水平升高。高剂量(100mg/kg)的槲皮素给药进一步加重了糖尿病病情(DQ100),但这种治疗对健康大鼠(NQ100)产生了有害影响,表明具有促氧化剂活性。然而,低剂量(10mg/kg)的槲皮素给药对 DQ100 中的 ICC、nNOS、巨噬细胞和氧化/抗氧化状态产生了抗氧化和保护作用,但 NQ100 在正常血糖动物中表现出罕见的负面结果。槲皮素的微囊化可能成为减少糖尿病引起的氧化应激的有前途的替代方法,但抗氧化治疗在健康状态下应谨慎使用,以避免毒性作用。