在蛋白质合成过程中草甘膦替代甘氨酸是中美洲肾病的一个致病因素

S. Seneff, L. Orlando
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引用次数: 4

摘要

中美洲肾病(MeN),也被称为病因不明的慢性肾脏疾病(CKDu),是一种影响中美洲农业工人的罕见肾脏疾病。在尼加拉瓜和萨尔瓦多的年轻男性甘蔗工人中,其患病率高得惊人。由于缺乏已知的CKD病因,如高血压和糖尿病,导致研究人员探索了许多潜在的危险因素,尽管没有充分解释该疾病的时间和流行性质。在本文中,我们探讨了草甘膦(一种常规用于甘蔗的除草剂)可能通过其编码氨基酸甘氨酸类似物的特性在MeN中发挥重要的因果作用的想法。草甘膦是一种甘氨酸分子,它的氮原子上连着一个甲基膦基。它取代甘氨酸可能会破坏多种对肾脏健康至关重要的蛋白质。在这里,我们首先从先前的研究文献中提出草甘膦可能错误地取代甘氨酸的证据。特别是,多种细菌和植物都发生了突变,去除了莽草酸途径中被草甘膦破坏的酶中高度保守的甘氨酸残基,这种突变导致酶对草甘膦完全不敏感。我们已经确定了多种与肾功能相关的关键蛋白,草甘膦替代关键甘氨酸残基对其的破坏可以解释MeN的大多数独特特征。具体来说,在水通道蛋白、氯离子通道、细胞色素C氧化酶和胶原蛋白等中的甘氨酸取代可能导致脱水、尿酸化增加、肾纤维化、横纹肌溶解和线粒体功能障碍。虽然草甘膦可能破坏蛋白质合成的假设尚未得到证实,但值得注意的是,它很好地解释了男性的多种特征。迫切需要进行调查,以验证草甘膦是否实际上破坏了蛋白质的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glyphosate Substitution for Glycine During Protein Synthesis as a Causal Factor in Mesoamerican Nephropathy
Mesoamerican Nephropathy (MeN), also known as Chronic Kidney Disease of unknown etiology (CKDu), is an unusual form of kidney disease affecting agricultural workers in Central America. Its prevalence is alarmingly high among young male sugarcane workers in Nicaragua and El Salvador. The absence of known etiologies for CKD, such as hypertension and diabetes, has led researchers to explore a number of potential risk factors, though none adequately explain the timing and epidemic nature of the disease. In this paper, we explore the idea that glyphosate, an herbicide routinely used on sugarcane, could play a significant causal role in MeN, mediated by its property as an analogue of the coding amino acid glycine. Glyphosate is a glycine molecule with a methyl phosphonyl group attached to its nitrogen atom. Its substitution in place of glycine could disrupt multiple proteins critical for kidney health. Here, we first present prior evidence from the research literature that glyphosate may be substituting erroneously for glycine. In particular, multiple species of both bacteria and plants have mutated to remove a highly conserved glycine residue in the enzyme in the shikimate pathway that is disrupted by glyphosate, and this mutation has caused the enzyme to be completely insensitive to glyphosate. We have identified multiple proteins with key roles related to kidney function, whose disruption by glyphosate substitution for critical glycine residues could explain most of the unique features of MeN. Specifically, glycine substitution in aquaporin, chloride channels, cytochrome C oxidase and collagen, among others, could contribute to dehydration, increased urinary acidification, renal fibrosis, rhabdomyolysis and mitochondrial dysfunction. While the hypothesis that glyphosate could be disrupting protein synthesis is not yet proven, it is remarkable how well it explains multiple features of MeN. Investigations to verify whether glyphosate is in fact disrupting protein synthesis are urgently needed.
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