Abstract

We previously reported that Tangshen formula (TSF), a Chinese herbal medicine for diabetic kidney disease (DKD) therapy, imparts renal protective effects. However, the underlying mechanisms of these effects remain unclear. Pyroptosis is a form of programmed cell death that can be triggered by the NLRP3 inflammasome. Recently, the association between the pyroptosis of renal resident cells and DKD was established, but with limited evidence. This study aimed to investigate whether the renal protective effects of TSF are related to its anti-pyroptotic effect. DKD rats established by right uninephrectomy plus a single intraperitoneal injection of STZ and HK-2 cells stimulated by AGEs were used. In vivo, TSF reduced the 24 h urine protein (24 h UP) of DKD rats and alleviated renal pathological changes. Meanwhile, the increased expression of pyroptotic executor (GSDMD) and NLRP3 inflammasome pathway molecules (NLRP3, caspase-1, and IL-1β) located in the tubules of DKD rats were downregulated with TSF treatment. In vitro, we confirmed the existence of pyroptosis in AGE-stimulated HK-2 cells and the activation of the NLRP3 inflammasome. TSF reduced pyroptosis and NLRP3 inflammasome activation in a dosage-dependent manner. Then, we used nigericin to determine that TSF imparts anti-pyroptotic effects by inhibiting the NLRP3 inflammasome. Finally, we found that TSF reduces reactive oxygen species (ROS) production and thioredoxin-interacting protein (TXNIP) expression in AGE-stimulated HK-2 cells. More importantly, TSF decreased the colocalization of TXNIP and NLRP3, indicating that ROS-TXNIP may be the target of TSF. In summary, the anti-pyroptotic effect via the TXNIP-NLRP3-GSDMD axis may be an important mechanism of TSF for DKD therapy.

Highlights

  • Diabetic kidney disease (DKD) is a severe microvascular complication of diabetes and is the leading cause of end-stage renal disease (Umanath and Lewis 2018)

  • Masson’s trichrome stain and semi-quantitative analysis showed enhanced tubulointerstitial fibrosis in diabetic kidney disease (DKD) rats compared with the control, which was attenuated in Tangshen formula (TSF)-treated rats (Figures 1D,F)

  • Periodic acid-Schiff (PAS) staining and semi-quantitative analysis showed that glomerular mesangial matrix expansion was enhanced in the DKD rats compared with the control; this enhancement was attenuated in DKD rats treated with TSF (Figures 1D,G)

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Summary

Introduction

Diabetic kidney disease (DKD) is a severe microvascular complication of diabetes and is the leading cause of end-stage renal disease (Umanath and Lewis 2018). The pyroptosis of renal resident cells has been associated with DKD. Pyroptosis is a type of programmed cell death that has recently been reported to occur in various diseases (Wang et al, 2019; Wu et al, 2019; Zhaolin et al, 2019; Yu et al, 2020a). The membrane protein gasdermin D (GSDMD) is a member of the gasdermin (GSDM) family, which has been shown to be the executor of pyroptosis (Aglietti and Dueber 2017; Feng et al, 2018). GSDMD can be cleaved by activated caspases into the N-and C-termini. Pyroptosis is considered as a type of inflammatory cell death (Broz et al 2020)

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