Department of Histology and Cell Biology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Department of Clinical Pharmacology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
CNS Neurosci Ther. 2022 May;28(5):732-748. doi: 10.1111/cns.13805. Epub 2022 Jan 23.
Parkinson's disease (PD) is the second most prevalent age-related neurodegenerative disorder. The cerebellum plays a role in PD pathogenesis. Curcumin has numerous medicinal uses, mostly attributed to its potent antioxidant properties. This study investigated the potential protective influence of curcumin on the cerebellum of albino rats with rotenone-induced PD.
Forty adult male albino rats were randomized into four treatment groups: vehicle (group I); rotenone 3 mg/kg/day i.p. injection (group II); rotenone 3 mg/kg/day plus curcumin 30 mg/kg/day i.p. injection (group III); and curcumin 30 mg/kg/day i.p. injection (group IV).
Compared to group I, group II exhibited marked degenerative changes in hematoxylin & eosin-stained sections and a reduction in Nissl granules in the Purkinje cells of the cerebellum. In group III, the neurotoxic effects in the cerebellum were reduced. Furthermore, the degenerated Purkinje and GFAP-positive cells increased considerably in group II and were partially reduced in group III versus group II. Compared to group I, rats in group II showed reduced rotarod motor activity, partially restored in group III. Acetylcholine esterase, glutathione, and superoxide dismutase were significantly reduced, and malondialdehyde was significantly increased in group II compared to group I and was partially increased in group III.
Curcumin attenuated neurotoxic effects and degenerative histological changes and alleviated induced oxidative stress in the cerebellar cortex of a PD rat model. Therefore, curcumin dietary supplementation may have neuroprotective effects against the development of cerebellum-related PD symptoms.
帕金森病(PD)是第二大常见的与年龄相关的神经退行性疾病。小脑在 PD 发病机制中起作用。姜黄素具有多种药用用途,主要归因于其强大的抗氧化特性。本研究调查了姜黄素对鱼藤酮诱导的 PD 白化大鼠小脑的潜在保护作用。
40 只成年雄性白化大鼠随机分为四组治疗组:载体(I 组);鱼藤酮 3mg/kg/天腹腔注射(II 组);鱼藤酮 3mg/kg/天加姜黄素 30mg/kg/天腹腔注射(III 组);和姜黄素 30mg/kg/天腹腔注射(IV 组)。
与 I 组相比,II 组在苏木精和伊红染色切片中表现出明显的退行性变化,小脑浦肯野细胞中的尼氏颗粒减少。在 III 组中,小脑的神经毒性作用减轻。此外,退化的浦肯野细胞和 GFAP 阳性细胞在 II 组中显著增加,在 III 组中与 II 组相比部分减少。与 I 组相比,II 组大鼠的旋转棒运动活性降低,在 III 组中部分恢复。与 I 组相比,乙酰胆碱酯酶、谷胱甘肽和超氧化物歧化酶显著降低,丙二醛显著增加,在 III 组中也部分增加。
姜黄素减轻了 PD 大鼠模型小脑的神经毒性作用和退行性组织学变化,并缓解了诱导的氧化应激。因此,姜黄素饮食补充可能对小脑相关 PD 症状的发展具有神经保护作用。