Insights into the protective capacity of human dental pulp stem cells and its secretome in cisplatin-induced nephrotoxicity: effects on oxidative stress and histological changes.

Q3 Pharmacology, Toxicology and Pharmaceutics Journal of Basic and Clinical Physiology and Pharmacology Pub Date : 2023-05-01 DOI:10.1515/jbcpp-2022-0159
Esmail Ranjbar, Jalil Tavakol Afshari, Abolfazl KhajaviRad, Alireza Ebrahimzadeh-Bideskan, Reyhaneh Shafieian
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Abstract

Objectives: Acute renal injury (AKI) is a major limiting factor for cisplatin administration. Recent evidence suggests the potential contribution of mesenchymal stem cells (MSCs) to rehabilitation from several disorders via both direct and indirect routes. Thus, the present study aimed, for the first time, to explore and compare the reno-protective potential of human dental pulp-derived stem cells (hDPSCs) vs. hDPSC-conditioned medium (hDPSC-CM) in recovery of impaired kidney tissues in a rat animal model of cisplatin-induced AKI.

Methods: AKI was induced via cisplatin injection (n=36). One day after, 24 rats were treated with either hDPSCs or hDPSC-CM (n=12). An extra set of rats (n=12) served as sham group. On days 2 or 7 (n=6), rats were humanly sacrificed for further analysis. Renal injury was explored via measuring serum creatinine and BUN. Renal level of oxidative stress was assessed by determining malondialdehyde, and enzymatic activities of superoxide dismutase and catalase. Renal histopathological changes were scored for comparison among different experimental groups.

Results: A single dose of cisplatin resulted in considerable renal dysfunction and oxidative stress. Treatment with hDPSCs or hDPSC-CM resulted in significantly restored renal function, reduced level of oxidative stress, and improved histopathological manifestations. Furthermore, as compared to hDPSC-CM, administration of hDPSCs led to superior results in AKI-induced animals.

Conclusions: The current study described the first comparative evidence of reno-protective potential of hDPSCs and their CM against cisplatin-induced nephrotoxicity in an AKI rat model, proposing them as useful adjunctive therapy in AKI. Yet, future explorations are still needed.

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人类牙髓干细胞及其分泌组在顺铂引起的肾毒性中的保护能力:对氧化应激和组织学改变的影响。
目的:急性肾损伤(AKI)是顺铂给药的主要限制因素。最近的证据表明,间充质干细胞(MSCs)通过直接和间接途径对几种疾病的康复有潜在的贡献。因此,本研究旨在首次探索并比较人牙髓源性干细胞(hdpsc)与hdpsc条件培养基(hDPSC-CM)在顺铂诱导的AKI大鼠动物模型中恢复受损肾组织的肾保护潜力。方法:采用顺铂注射液诱导AKI(36例)。1 d后,24只大鼠分别接受hdpsc或hDPSC-CM治疗(n=12)。另取12只大鼠作为假手术组。在第2天或第7天(n=6),处死大鼠作进一步分析。测定血清肌酐和尿素氮,探讨肾损伤情况。通过测定丙二醛、超氧化物歧化酶和过氧化氢酶的酶活性来评估肾脏氧化应激水平。对各实验组肾脏组织病理变化进行评分比较。结果:单剂量顺铂可导致严重的肾功能障碍和氧化应激。用hdpsc或hDPSC-CM治疗可显著恢复肾功能,降低氧化应激水平,改善组织病理表现。此外,与hDPSC-CM相比,hdpsc在aki诱导的动物中具有更好的效果。结论:目前的研究描述了hdpsc及其CM在AKI大鼠模型中对顺铂诱导的肾毒性的肾保护潜力的第一个比较证据,提出它们是AKI的有用辅助治疗。然而,未来的探索仍然需要。
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来源期刊
Journal of Basic and Clinical Physiology and Pharmacology
Journal of Basic and Clinical Physiology and Pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
3.90
自引率
0.00%
发文量
53
期刊介绍: The Journal of Basic and Clinical Physiology and Pharmacology (JBCPP) is a peer-reviewed bi-monthly published journal in experimental medicine. JBCPP publishes novel research in the physiological and pharmacological sciences, including brain research; cardiovascular-pulmonary interactions; exercise; thermal control; haematology; immune response; inflammation; metabolism; oxidative stress; and phytotherapy. As the borders between physiology, pharmacology and biochemistry become increasingly blurred, we also welcome papers using cutting-edge techniques in cellular and/or molecular biology to link descriptive or behavioral studies with cellular and molecular mechanisms underlying the integrative processes. Topics: Behavior and Neuroprotection, Reproduction, Genotoxicity and Cytotoxicity, Vascular Conditions, Cardiovascular Function, Cardiovascular-Pulmonary Interactions, Oxidative Stress, Metabolism, Immune Response, Hematological Profile, Inflammation, Infection, Phytotherapy.
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