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黄曲霉毒素 A 在肾脏中的转运的分子机制。

Molecular mechanism of ochratoxin a transport in the kidney.

机构信息

Department of Pharmacology and Toxicology, Kyorin University School of Medicine, 6-20-2, Shinkawa, Mitaka-shi, Tokyo 181-8611, Japan.

出版信息

Toxins (Basel). 2010 Jun;2(6):1381-98. doi: 10.3390/toxins2061381. Epub 2010 Jun 9.

Abstract

The mycotoxin, ochratoxin A (OTA), is thought to be responsible for Balkan endemic nephropathy. OTA accumulates in several tissues, especially in the kidneys and liver. The excretion of OTA into urine is thought to be mainly by tubular secretion, presumably via the organic anion transport system. Recently, several families of multispecific organic anion transporters have been identified: organic anion transporters (OATs), organic anion-transporting polypeptides (OATPs), oligopeptide transporters (PEPTs), and ATP-binding cassette (ABC) transporters, such as MRP2 and BCRP. These renal transporters mediate the transmembrane transport of OTA and play a pivotal role in the development of OTA-induced nephrotoxicity.

摘要

真菌毒素赭曲霉毒素 A(OTA)被认为是巴尔干地方性肾病的罪魁祸首。OTA 会在多种组织中积累,尤其是在肾脏和肝脏中。OTA 主要通过肾小管分泌的方式排泄到尿液中,推测是通过有机阴离子转运系统。最近,已经鉴定出几种多特异性有机阴离子转运体家族:有机阴离子转运体(OATs)、有机阴离子转运多肽(OATPs)、寡肽转运体(PEPTs)和 ATP 结合盒(ABC)转运体,如 MRP2 和 BCRP。这些肾脏转运体介导 OTA 的跨膜转运,在 OTA 诱导的肾毒性发展中起着关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1826/3153260/cfddbcb30158/toxins-02-01381-g001.jpg

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