Mascarenhas Starlaine, Mutnuri Srikanth, Ganguly Anasuya
Department of Biological Sciences, BITS Pilani, K K Birla Goa Campus, NH 17 B, Zuarinagar, Goa, 403 726, India.
Chemosphere. 2017 Jun;177:239-249. doi: 10.1016/j.chemosphere.2017.02.155. Epub 2017 Mar 1.
Chronic-Kidney-Disease of Unknown-etiology (CKDu) has been reported in developing-countries like Sri-Lanka, India and Central-America without sparing the Indian sub-district (namely Canacona) located in south-Goa. The disease etiology is unlinked to common causes of diabetes and hypertension and assumed to be environmentally induced due to its asymptomatic-nature and occurrence in groundwater relying communities. This study aimed to understand environmental risk-factors underlying CKDu-etiology using Indian sub-district (Canacona) as case-study. Biochemical-analysis of CKDu-affected and non-affected individual's blood and detailed hydro-geochemical analyses of CKDu-affected and non-affected region's groundwater (drinking-water)were conducted. Trace geogenic-element-silica was highly dominant in affected-region's groundwater, thus its nephrotoxic-potential was analysed via in-vitro cytotoxicity-assays on human-kidney-cell-lines. All CKDu-affected-subjects showed increased-levels of serum-urea (52.85 mM),creatinine (941.5 μM),uric-acid (1384.5 μM), normal blood-glucose (4.65 mM), being distinct biomarkers of environmentally-induced CKD-'chronic-tubulo-interstitial-nephritis'. Affected-subjects reported high blood-lead levels (1.48 μM)suggesting direct-nephrotoxicity resulting in impaired blood-clearance and also exhibits indirect-nephrotoxicity by disrupting calcium-homeostasis causing skeletal-disorders and prolonged-consumption of NSAID's (pain-alleviation), indirectly causing renal-damage. Affected-region's groundwater was acidic (pH-5.6), resulting in borderline-lead (9.98 μgL) and high-silica (115.5 mgL)contamination. Silica's bio-availability (determining its nephrotoxicity) was enhanced at groundwater's acidic-pH and Ca-Mg-deficient-composition (since these cations complex with silica reducing bioavailability). Silica exhibited renal-proximal-tubular-cytotoxicity on long-term exposure comparable with affected-region's groundwater silica-levels, by apoptosis-mediated-cell-death resulting in tubular-atrophy, interstitial-fibrosis and irreversible renal-damage (CKD). Thus this study provides novel-insights into nephrotoxic-potential of trace-geogenic-element-silica in CKDu causation. It highlights direct-indirect nephrotoxicity exhibited by lead at low-levels due to its bio-accumulative-capacity. Silica's nephrotoxic-potential can be considered when deciphering etiology of CKDu-problem in developing-countries (relying on groundwater).
在斯里兰卡、印度和中美洲等发展中国家均有不明病因的慢性肾脏病(CKDu)的报道,印度果阿邦南部的一个印度次分区(即卡纳科纳)也未能幸免。该疾病的病因与糖尿病和高血压等常见病因无关,由于其无症状的性质以及在依赖地下水的社区中出现,因此被认为是由环境因素诱发的。本研究旨在以印度次分区(卡纳科纳)为案例研究,了解CKDu病因背后的环境风险因素。对受CKDu影响和未受影响个体的血液进行了生化分析,并对受CKDu影响和未受影响地区的地下水(饮用水)进行了详细的水文地球化学分析。痕量地质成因元素硅在受影响地区的地下水中高度占主导地位,因此通过对人肾细胞系进行体外细胞毒性试验分析了其肾毒性潜力。所有受CKDu影响的受试者血清尿素(52.85 mM)、肌酐(941.5 μM)、尿酸(1384.5 μM)水平升高,血糖正常(4.65 mM),这些都是环境诱发的CKD——慢性肾小管间质性肾炎的明显生物标志物。受影响的受试者报告血铅水平较高(1.48 μM),表明直接肾毒性导致血液清除受损,并且通过破坏钙稳态导致骨骼疾病以及长期服用非甾体抗炎药(缓解疼痛)间接引起肾损伤,进而表现出间接肾毒性。受影响地区的地下水呈酸性(pH值为5.6),导致铅含量接近临界值(9.98 μg/L)和高硅含量(115.5 mg/L)污染。在地下水酸性pH值和钙镁缺乏的成分条件下(因为这些阳离子与硅络合会降低生物利用度),硅的生物利用度(决定其肾毒性)会增强。长期接触时,硅表现出与受影响地区地下水中硅水平相当的近端肾小管细胞毒性,通过凋亡介导的细胞死亡导致肾小管萎缩、间质纤维化和不可逆转的肾损伤(CKD)。因此,本研究为痕量地质成因元素硅在CKDu病因中的肾毒性潜力提供了新的见解。它突出了铅由于其生物累积能力在低水平时表现出的直接和间接肾毒性。在解读发展中国家(依赖地下水)CKDu问题的病因时,可以考虑硅的肾毒性潜力。