BioMed Research International · 2015 · 17 citations · 29 references
PharmacyPharmacologyToxicologyHeavy Metal ToxicologyRenal PathophysiologyRenal PharmacokineticsArsenic PoisoningArsenic ToxicologyHeavy Metal NeurotoxicityMercury PoisoningMercury ToxicologyRenal ToxicityMechanisms Of Arsenic ToxicityMechanisms Of Renal ToxicityMercury Toxicity MechanismsMercury-induced Renal ToxicityPharmacokinetic ParametersReal-time Polymerase Chain Reaction (Pcr)Renal Toxicity Of ArsenicTraditional Chinese Medicine
Toxic heavy metals, including mercury (Hg) and arsenic (As), accumulate preferentially in kidneys and always cause acute renal failure. The aim of this study was to investigate whether these samples affect organic anion transporters, Oat1 and Oat3, in vivo in mice kidney. Mice (n = 10) were orally treated with investigational samples. After last administration, all mice were i.v. p-aminohippuric acid (PAH), and the blood and kidneys samples were collected. The concentrations of PAH were quantified by spectrophotometry. mRNA expressions of Oat1 and Oat3 were assayed by real-time PCR. In comparison with corresponding control, major pharmacokinetic parameters of PAH in sera were significantly changed by investigational samples (p < 0.05), PAH accumulations in the kidney tissues were significantly higher (p < 0.05), PAH uptake by renal slices was greatly reduced, Oat1 and Oat3 mRNA expression were significantly inhibited in investigational sample groups. Arsenic and mercury containing traditional Chinese medicine (Realgar and Cinnabar) probably induce kidney damage through inhibiting several members of the organic anion transporters (such as OAT1 and OAT3).
29
Chutima Srimaroeng, Jennifer Perry Cecile, Ramsey Walden et al. · Cellular Physiology and Biochemistry · 2013 · 3K citations · Full text
Adriamycin-induced nephrotic syndrome in rats: sequence of pathologic events.
Tullio Bertani, Alessandro Poggi, R Pozzoni et al. · PubMed · 1982 · 372 citations
Medicine, Nephrology, Pharmacology +11