4.7 Article

Synergistic interaction of effective parts in Rehmanniae Radix and Corpus officinalis ameliorates renal injury in C57BL/KsJ-db/db diabetic mice: Involvement of suppression of AGEs/RAGE/SphK1 signaling pathway

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 185, Issue -, Pages 110-119

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2016.03.017

Keywords

Rehmanniae Radix; Corpus officinalis; Iridoid glycoside; Triterpenoid acid; Diabetic nephropathy; AGEs/RAGE/SphK1 signaling pathway

Funding

  1. National Natural Science Foundation of China [81073111]
  2. Priority Academic Program Development of Jiangsu Higher Education Institutions [nzyzyxjp1006]

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Ethnopharmacological relevance: Rehmanniae Radix (RR) and Corpus officinalis (CO) are two traditional Chinese medicines widely used in China for treating diabetes mellitus and its complications, such as diabetic nephropathy. Iridoid glycoside of Corpus officinalis (IGCO), triterpenoid acid of Cornus officinalis (TACO) and iridoid glycoside of Rehmanniae Radix (IGRR) formed an innovative formula named combinatorial bioactive parts (CBP). The aims of the present study were to investigate the renoprotective effects of CBP on DN through the inhibition of AGEs/RAGE/SphK1 signaling pathway activation, and identify the advantage of CBP compared with IGCO, TACO, IGRR. Materials and methods: The db/db diabetic renal injury model was used to examine the renoprotective effects of CBP, IGCO, TACO and IGRR. For mechanistic studies, diabetic symptoms, renal functions, and pathohistology of pancreas and kidney were evaluated. AGEs/RAGE/SphK1 pathway were determined. Results: CBP, IGCO, TACO and IGRR inhibited the decrease in serum insulin levels and the increases in urine volume, food consumption, water intake, TC, TG, glycated serum protein, fasting blood glucose levels, 24 h urine protein levels, and serum levels of urea nitrogen and creatinine. It also prevented ECM accumulation and improved the histology of pancreas and kidney, and alleviated the structural alterations in mesangial cells and podocytes in renal cortex. Moreover, CBP, IGCO, TACO and IGRR down regulated the elevated staining, protein levels of RAGE, SphK1, TGF-beta and NF-kappa B. Among the treatment groups, CBP produced the strongest effects. Conclusions: These findings suggest that the inhibitory effect of CBP, IGCO, TACO and IGRR on the activation of AGEs/RAGE/SphK1 signaling pathway in db/db diabetic mice kidney is a novel mechanism by which CBP, IGCO, TACO and IGRR exerts renoprotective effects on DN. Among all the groups, CBP produced the strongest effect while IGCO, TACO and IGRR produced weaker effects. (C) 2016 Elsevier Ireland Ltd. All rights reserved.

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