Literature DB >> 21881242

The ameliorative effect of 23-hydroxytormentic acid isolated from Rubus coreanus on cisplatin-induced nephrotoxicity in rats.

Se-Il Sohn1, Hong-Kun Rim, Yang-Hee Kim, Jung-Hye Choi, Jae-Hoon Park, Hee-Juhn Park, Jong-Won Choi, Soo-Dong Kim, Seo-Young Jeong, Kyung-Tae Lee.   

Abstract

Previously, the authors demonstrated that the triterpenoid glycoside niga-ichigoside F₁ (NIF₁) and its aglycone 23-hydroxytormentic acid (23-HTA) isolated from the unripe fruits of Rubus coreanus (Rosaceae) ameliorate cisplatin-induced toxicity in renal epithelial LLC-PK₁ cells. In the present study, the nephroprotective effects of NIF₁ and 23-HTA were investigated in Sprague-Dawley rats with acute renal injury induced by a single intraperitoneal (i.p.) injection of cisplatin (7 mg/kg). Pretreatment with 23-HTA (10 mg/kg/d, per os (p.o.)) significantly reduced cisplatin-induced elevations in blood urea nitrogen (BUN) and serum creatinine level, whereas NIF₁ (10 mg/kg, p.o.) slightly reduced these levels. In addition, pretreatment with 23-HTA prevented cisplatin-induced hydroxyl radical generation, malondialdehyde (MDA) production, glutathione (GSH) depletion, and cisplatin-induced changes in the activities of oxidant and antioxidant enzymes in rat renal tissues. In addition, histopathological examinations showed that 23-HTA pretreatment reduced cisplatin-induced acute tubular necrosis and histological changes. In contrast, NIF₁ was found to have a slight or no influence on cisplatin-induced oxidative enzymes and acute tubular necrosis. Taken together, these results suggest that protective effect of 23-HTA pretreatment on cisplatin-induced renal damage is associated with the attenuation of oxidative stress and the preservation of antioxidant enzymes.

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Year:  2011        PMID: 21881242     DOI: 10.1248/bpb.34.1508

Source DB:  PubMed          Journal:  Biol Pharm Bull        ISSN: 0918-6158            Impact factor:   2.233


  3 in total

1.  23-Hydroxytormentic acid reduces cerebral ischemia/reperfusion damage in rats through anti-apoptotic, antioxidant, and anti-inflammatory mechanisms.

Authors:  Yamin Wang; Fengrong Liu; Peng Liu
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2021-01-04       Impact factor: 3.000

2.  Bone marrow-derived mesenchymal stem cells protect against cisplatin-induced acute kidney injury in rats by inhibiting cell apoptosis.

Authors:  Shaohua Qi; Dongcheng Wu
Journal:  Int J Mol Med       Date:  2013-10-08       Impact factor: 4.101

Review 3.  Plant-Derived Agents for Counteracting Cisplatin-Induced Nephrotoxicity.

Authors:  Shreesh Ojha; Balaji Venkataraman; Amani Kurdi; Eglal Mahgoub; Bassem Sadek; Mohanraj Rajesh
Journal:  Oxid Med Cell Longev       Date:  2016-09-27       Impact factor: 6.543

  3 in total

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