Evidence-based Complementary and Alternative Medicine · 2015 · 17 citations · 33 references
MedicineNephrologyPathobiologyRenal PathologyRenal PathophysiologyRenal PharmacotherapyAcute Kidney InjuryGlomerular PathophysiologyPodocyte InjuryRenal DiseaseRenal InflammationRenal ProtectionAcute Kidney Injury PathophysiologyAssayHerbal Medicine NephrotoxicityNephrin SignalingPodocyte BiologyProtective TreatmentsReduced NephrotoxicityRenal Cortex Distribution
Objectives. We investigated the action of triptolide in rats with adriamycin-induced nephropathy and evaluated the possible mechanisms underlying its protective effect against podocyte injury. Methods. In total, 30 healthy male Sprague-Dawley rats were randomized into three groups (normal group, model group, and triptolide group). On days 7, 28, 42, and 56, 24 h urine samples were collected. All rats were sacrificed on day 56, and their blood and renal tissues were collected for determination of biochemical and molecular biological parameters. Expression of miRNAs in the renal cortex was analyzed by a biochip assay and RT-PCR was used to confirm observed differences in miRNA levels. Results. Triptolide decreased proteinuria, improved renal function without apparent adverse effects on the liver, and alleviated renal pathological lesions. Triptolide also elevated the nephrin protein level. Furthermore, levels of miR-344b-3p and miR-30b-3p were elevated in rats with adriamycin-induced nephropathy, while triptolide treatment reversed the increase in the expression of these two miRNAs. Conclusions. These results suggest that triptolide may attenuate podocyte injury in rats with adriamycin-induced nephropathy by regulating expression of miRNA-344b-3p and miRNA-30b-3p.
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