Krogh P
Royal Dental College, Copenhagen, Denmark.
Food Chem Toxicol. 1992 Mar;30(3):213-24. doi: 10.1016/0278-6915(92)90036-k.
Under experimental conditions renal damage has been induced by alimentary exposure to ochratoxin A in all single-stomach animals tested so far, including rodents, dogs, pigs and birds, and even in young ruminants still functioning as single-stomach animals. Most information on ochratoxin-induced nephropathy has been obtained in pigs during experimental studies comprising structural as well as functional changes. The renal damage is characterized morphologically by atrophy of the proximal tubules, interstitial cortical fibrosis and sclerotized glomeruli, and functionally by impairment of tubular function indicated by a decrease in TmPAH/Cin and reduced ability to produce concentrated urine. The renal effect has been observed using exposure levels of ochratoxin A in the range 200 to 4000 micrograms/kg feed. Field cases of ochratoxin-induced nephropathy in pigs have been encountered in many countries, and the disease mycotoxic porcine nephropathy (MPN) is recognized as an endemic disease entity in several northern and central European countries. Epidemics of MPN have been reported, closely related to excessive climatic conditions in periods preceding harvest. Ochratoxin A is a recognized renal carcinogen in the mouse. In female pigs exposed to alimentary ochratoxin A for 2 years, no renal cancer was observed. Ochratoxin A is metabolized and excreted relatively fast in animals, with an RL50 (residue elimination) in the pig of a few days for various tissues. Past exposure data is a requirement in retrospective epidemiological studies, but because of the short RL50 values tissue analysis for ochratoxin A is unlikely to provide that kind of data, in animals or in humans. In order to meet this demand a procedure has been developed, using renal biopsy material for activity analysis of two renal tubular enzymes, phosphoenolpyruvate carboxykinase and gamma-glutamyl transpeptidase. In pigs exposed to ochratoxin A for 1 week a 40% reduction of the enzyme activity was observed. The dose-related activity decrease of the two enzymes was accompanied by a dose-related aggravation of renal impairment, as measured by a reduction of TmPAH/Cin, suggesting that these enzymes are sensitive indicators of ochratoxin A-induced nephropathy.
在实验条件下,迄今所有接受测试的单胃动物,包括啮齿动物、狗、猪和鸟类,甚至在仍作为单胃动物的幼龄反刍动物中,通过经口接触赭曲霉毒素A均可诱发肾损伤。关于赭曲霉毒素诱发肾病的大多数信息是在猪的实验研究中获得的,这些研究包括结构和功能变化。肾损伤在形态学上的特征是近端小管萎缩、皮质间质纤维化和肾小球硬化,在功能上的特征是肾小管功能受损,表现为TmPAH/Cin降低和浓缩尿液能力下降。在饲料中赭曲霉毒素A的暴露水平为200至4000微克/千克时观察到了肾脏效应。在许多国家都发现了猪的赭曲霉毒素诱发肾病的田间病例,并且在北欧和中欧的几个国家,这种疾病——霉菌毒素性猪肾病(MPN)被认为是一种地方病实体。已经报道了MPN的流行,这与收获前时期的极端气候条件密切相关。赭曲霉毒素A在小鼠中是一种公认的肾致癌物。在经口接触赭曲霉毒素A两年的雌性猪中,未观察到肾癌。赭曲霉毒素A在动物体内代谢和排泄相对较快,猪体内各种组织的RL50(残留消除)为几天。既往暴露数据是回顾性流行病学研究的一项要求,但由于RL50值较短,对动物或人类进行赭曲霉毒素A的组织分析不太可能提供此类数据。为了满足这一需求,已开发出一种程序,使用肾活检材料对两种肾小管酶——磷酸烯醇丙酮酸羧激酶和γ-谷氨酰转肽酶进行活性分析。在接触赭曲霉毒素A一周的猪中,观察到酶活性降低了40%。这两种酶的活性随剂量降低,同时伴随着以TmPAH/Cin降低衡量的肾损伤的剂量相关性加重,表明这些酶是赭曲霉毒素A诱发肾病的敏感指标。