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锌作为镉毒性的对策。

Zinc as a countermeasure for cadmium toxicity.

机构信息

The First Hospital of Jilin University, Changchun, 130021, China.

Pediatric Research Institute, Department of Pediatrics, University of Louisville School of Medicine, Louisville, KY, 40202, USA.

出版信息

Acta Pharmacol Sin. 2021 Mar;42(3):340-346. doi: 10.1038/s41401-020-0396-4. Epub 2020 Apr 13.

DOI:10.1038/s41401-020-0396-4
PMID:32284539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8027184/
Abstract

Cadmium (Cd) is an important environmental pollutant and long-term Cd exposure is closely related to autoimmune diseases, cancer, cardiovascular diseases (CVD), and hepatic dysfunction. Zinc (Zn) is an essential metal that plays key roles in protein structure, catalysis, and regulation of their function. Numerous studies have shown that Zn can reduce Cd toxicity; however, the underlying mechanisms have not been extensively explored. Preclinical studies have revealed direct competition for sarcolemmal uptake between these two metals. Multiple sarcolemmal transporters participate in Cd uptake, including Zn transporters, calcium channels, and DMT1 (divalent metal transporter 1). Zn also induces several protective mechanisms, including MT (metallothionein) induction and favorable redox homeostasis. This review summarizes current knowledge related to the role of Zn and metal transporters in reducing Cd toxicity and discusses potential future directions of related research.

摘要

镉 (Cd) 是一种重要的环境污染物,长期接触镉与自身免疫性疾病、癌症、心血管疾病 (CVD) 和肝功能障碍密切相关。锌 (Zn) 是一种必需的金属,在蛋白质结构、催化和调节其功能方面发挥着关键作用。大量研究表明,锌可以降低镉的毒性;然而,其潜在机制尚未得到广泛探索。临床前研究表明,这两种金属在细胞膜摄取过程中存在直接竞争。多种细胞膜转运蛋白参与镉的摄取,包括锌转运蛋白、钙通道和 DMT1(二价金属转运蛋白 1)。锌还诱导多种保护机制,包括 MT(金属硫蛋白)诱导和有利的氧化还原稳态。本文综述了锌和金属转运体在降低镉毒性中的作用的相关知识,并讨论了相关研究的潜在未来方向。

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本文引用的文献

1
Zinc protects against cadmium-induced toxicity in neonatal murine engineered cardiac tissues via metallothionein-dependent and independent mechanisms.锌通过金属硫蛋白依赖和非依赖机制保护新生鼠工程化心脏组织免受镉诱导的毒性。
Acta Pharmacol Sin. 2020 May;41(5):638-649. doi: 10.1038/s41401-019-0320-y. Epub 2019 Nov 25.
2
Heavy metal toxicity: An update of chelating therapeutic strategies.重金属毒性:螯合治疗策略的最新进展。
J Trace Elem Med Biol. 2019 Jul;54:226-231. doi: 10.1016/j.jtemb.2019.05.003. Epub 2019 May 10.
3
Cadmium exposure in living organisms: A short review.镉在生物体中的暴露:一个简短的综述。
Sci Total Environ. 2019 Aug 15;678:761-767. doi: 10.1016/j.scitotenv.2019.04.395. Epub 2019 May 2.
4
Maintenance of Intestinal Epithelial Homeostasis by Zinc Transporters.锌转运体维持肠道上皮细胞稳态
Dig Dis Sci. 2019 Sep;64(9):2404-2415. doi: 10.1007/s10620-019-05561-2. Epub 2019 Mar 4.
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Glutathione Might Attenuate Cadmium-Induced Liver Oxidative Stress and Hepatic Stellate Cell Activation.谷胱甘肽可能减轻镉诱导的肝脏氧化应激和肝星状细胞活化。
Biol Trace Elem Res. 2019 Oct;191(2):443-452. doi: 10.1007/s12011-019-1641-x. Epub 2019 Feb 4.
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Involvement of the synapse-specific zinc transporter ZnT3 in cadmium-induced hippocampal neurotoxicity.突触特异性锌转运体ZnT3参与镉诱导的海马神经毒性。
J Cell Physiol. 2019 Sep;234(9):15872-15884. doi: 10.1002/jcp.28245. Epub 2019 Feb 4.
7
Channels, transporters and receptors for cadmium and cadmium complexes in eukaryotic cells: myths and facts.真核细胞中镉和镉配合物的通道、转运体和受体:神话与事实。
Biometals. 2019 Jun;32(3):469-489. doi: 10.1007/s10534-019-00176-6. Epub 2019 Jan 30.
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Negative effects of acute cadmium on stress defense, immunity, and metal homeostasis in liver of zebrafish: The protective role of environmental zinc dpre-exposure.急性镉对斑马鱼肝脏应激防御、免疫和金属内稳态的负面影响:环境锌预先暴露的保护作用。
Chemosphere. 2019 May;222:91-97. doi: 10.1016/j.chemosphere.2019.01.111. Epub 2019 Jan 21.
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Free Radic Biol Med. 2019 Apr;134:311-326. doi: 10.1016/j.freeradbiomed.2019.01.006. Epub 2019 Jan 6.
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Proteomic Analysis of Zn Depletion/Repletion in the Hormone-Secreting Thyroid Follicular Cell Line FRTL-5.Zn 耗竭/补充的蛋白质组学分析在激素分泌甲状腺滤泡细胞系 FRTL-5 中。
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