4.7 Article

Salvia miltiorrhiza Bunge (Danshen) and Bioactive Compound Tanshinone IIA Alleviates Cisplatin-Induced Acute Kidney Injury Through Regulating PXR/NF-κB Signaling

Journal

FRONTIERS IN PHARMACOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2022.860383

Keywords

acute kidney injury; pregnane X receptor; NF-kappa B; Salvia miltiorrhiza; tanshinone IIA; renal inflammation

Funding

  1. National Natural Science Foundation of China [81903956]
  2. China Postdoctoral Science Foundation [2021M690042]
  3. Project of Guangdong Province Administration of Traditional Chinese Medicine [20201133]
  4. Basic and Applied Basic Research Project of Guangzhou Science and Technology Department [202102020011]

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This study aimed to reveal the potential protective role of Salvia miltiorrhiza Bunge (Danshen) and its bioactive compound Tanshinone IIA (TanIIA) in acute kidney injury (AKI) and investigate the specific regulatory function of PXR/NF-kappa B signaling in AKI-induced renal inflammation. Network pharmacological analysis identified nuclear receptors as potential therapeutic targets of Salvia miltiorrhiza in AKI treatment. In vivo and in vitro experiments demonstrated that TanIIA improved renal function and reduced inflammation by regulating PXR/NF-kappa B signaling. The findings suggest PXR as a potential therapeutic target for AKI.
Objective: The present study aims to provide evidence on the potential protective role of Salvia miltiorrhiza Bunge (Danshen) and its bioactive compound Tanshinone IIA (TanIIA) in AKI and to reveal the specific regulatory function of PXR/NF-kappa B signaling in AKI-induced renal inflammation.& nbsp;Methods: A network pharmacological analysis was used to study target genes and regulatory networks in the treatment of Salvia miltiorrhiza on AKI. Further experiments with in vivo AKI mouse model and in vitro studies were applied to investigate the renal protective effect of TanIIA in AKI. The mechanisms of TanIIA regulating PXR/NF-kappa B signaling in renal inflammation were also studied.& nbsp;Results: Network pharmacology had suggested the nuclear receptor family as new therapeutic targets of Salvia miltiorrhiza in AKI treatment. The in vivo studies had demonstrated that TanIIA improved renal function and inflammation by reducing necrosis and promoting the proliferation of tubular epithelial cells. Improved renal arterial perfusion in AKI mice with TanIIA treatment was also recorded by ultrasonography. In vitro studies had shown that TanIIA ameliorated renal inflammation by activating the PXR while inhibiting PXR-mediated NF-kappa B signaling. The results had suggested a role of PXR activation against AKI-induced renal inflammation.& nbsp;Conclusion: Salvia miltiorrhiza Bunge (Danshen) may protect the kidneys against AKI by regulating nuclear receptors. TanIIA improved cell necrosis proliferation and reduced renal inflammation by upregulating the expression of the PXR and inhibiting NF-kappa B signaling in a PXR-dependent manner. The PXR may be a potential therapeutic target for AKI treatment.

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