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大豆饮食可防止镉进入大鼠小脑,维持微量元素的体内平衡,避免形态改变。

A soybean based-diet prevents Cadmium access to rat cerebellum, maintaining trace elements homeostasis and avoiding morphological alterations.

机构信息

Laboratory of Nutrition, Environment and Cell Metabolism, Faculty of Chemistry, Biochemistry and Pharmacy, National University of San Luis, Argentina and IMIBIO-SL CONICET, San Luis, Argentina.

IMIBIO-SL CONICET, San Luis, Argentina.

出版信息

Biometals. 2023 Feb;36(1):67-96. doi: 10.1007/s10534-022-00462-w. Epub 2022 Nov 14.

Abstract

Cadmium (Cd) is one of the most dangerous heavy metals that exists. A prolonged exposure to Cd causes toxic effects in a variety of tissues, including Central Nervous System (CNS), where it can penetrate the Blood Brain Barrier (BBB). Cd exposure has been linked to neurotoxicity and neurodegenerative diseases. Soy isoflavones have a strong antioxidant capacity, and they have been shown to have positive effects on cognitive function in females. However, the mechanisms underlying Cd neurotoxicity remain completely unresolved. The purpose of this study was to characterize the potential protective effect of a soy-based diet vs. a casein-based diet against Cd toxicity in rat cerebellum. Female Wistar rats were fed with casein (Cas) or soybean (So) as protein sources for 60 days. Simultaneously, half of the animals were administered either 15 ppm of Cadmium (CasCd and SoCd groups) in water or regular tap water as control (Cas and So groups). We analyzed Cd exposure effects on trace elements, oxidative stress, cell death markers, GFAP expression and the histoarchitecture of rat cerebellum. We found that Cd tissue content only augmented in the Cas intoxicated group. Zn, Cu, Mn and Se levels showed modifications among the different diets. Expression of Nrf-2 and the activities of CAT and GPx decreased in Cas and So intoxicated groups,while 3-NT expression increased only in the CasCd group. Morphometry analyses revealed alterations in the purkinje and granular cells morphology, decreased number of granular cells and reduced thickness of the granular layer in Cd-intoxicated rats, whereas no alterations were observed in animals under a So diet. In addition, mRNA expression of apoptotic markers BAX/Bcl-2 ratio and p53 expression increased only in the CasCd group, a finding confirmed by positive TUNEL staining in the cerebellum granule cell layer in the same group. Also, Cd intoxication elicited overexpression of GFAP by astrocytes, which was prevented by soy. White matter alterations were only subtle and characterized by intramyelinic edema in the CasCd group. Overall, these results unmask an irreversible toxic effect of a subchronic Cd intoxication on the cerebellum, and identify a protective role by a soy-based diet with potential as a therapeutic strategy for those individuals exposed to this dangerous environmental contaminant.

摘要

镉(Cd)是存在的最危险的重金属之一。长期接触 Cd 会导致多种组织的毒性作用,包括中枢神经系统(CNS),它可以穿透血脑屏障(BBB)。Cd 暴露与神经毒性和神经退行性疾病有关。大豆异黄酮具有很强的抗氧化能力,已被证明对女性的认知功能有积极影响。然而,Cd 神经毒性的机制仍未完全解决。本研究的目的是描述基于大豆的饮食与基于酪蛋白的饮食对大鼠小脑 Cd 毒性的潜在保护作用。雌性 Wistar 大鼠用酪蛋白(Cas)或大豆(So)作为蛋白质来源喂养 60 天。同时,一半的动物给予水中的 15ppm Cd(CasCd 和 SoCd 组)或作为对照的自来水(Cas 和 So 组)。我们分析了 Cd 暴露对微量元素、氧化应激、细胞死亡标志物、GFAP 表达和大鼠小脑组织形态的影响。我们发现,只有在 Cas 中毒组中,Cd 组织含量才会增加。不同饮食中 Zn、Cu、Mn 和 Se 水平发生了变化。Cas 和 So 中毒组中 Nrf-2 表达和 CAT 和 GPx 活性降低,而只有在 CasCd 组中 3-NT 表达增加。形态计量学分析显示,Cd 中毒大鼠浦肯野和颗粒细胞形态发生改变,颗粒细胞数量减少,颗粒层厚度减小,而在大豆饮食组中未观察到改变。此外,仅在 CasCd 组中,凋亡标志物 BAX/Bcl-2 比值和 p53 表达的 mRNA 表达增加,这一发现通过 CasCd 组小脑颗粒细胞层的 TUNEL 阳性染色得到证实。此外,Cd 中毒引起星形胶质细胞 GFAP 过度表达,而大豆则可预防这种过度表达。只有 CasCd 组出现轻微的白质改变,特征为髓鞘内水肿。总的来说,这些结果揭示了亚慢性 Cd 中毒对小脑的不可逆毒性作用,并确定了基于大豆的饮食的保护作用,这可能是对暴露于这种危险环境污染物的个体的一种治疗策略。

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