Involvement of NLRP3 inflammasome in the impacts of sodium and potassium on insulin resistance in normotensive Asians. Issue 2 (23rd January 2018)

• Record Type: Journal Article
• Authors: Wan, Zhaofei; Wen, Wen; Ren, Keyu; Zhou, Dong; Liu, Junhui; Wu, Yue; Zhou, Juan; Mu, Jianjun; Yuan, Zuyi
• Is Part Of: British journal of nutrition. Volume 119:Issue 2(2018)
• Page Start: 228
• Page End: 237
• Publication Date: 2018-01-23
• Subjects: Insulin resistance, -- NLRP3 inflammasome, -- Oxidative stress, -- Sodium, -- Potassium; Nutrition -- Periodicals; 572.4
• DOI: 10.1017/S0007114517002926
• Languages: English
• ISSNs: 0007-1145

Abstract

Abstract: Salt, promoting oxidative stress, contributes to insulin resistance, whereas K, inhibiting oxidative stress, improves insulin sensitivity. Oxidative stress activation of NLRP3 inflammasome is a central player in the induction of insulin resistance. Therefore, we hypothesised that NLRP3 inflammasome may mediate the effects of salt and K on insulin resistance. In all, fifty normotensive subjects were recruited from a rural community of Northern China. The protocol included a low-salt diet for 7 d, then a high-salt diet for 7 d and a high-salt diet with K supplementation for another 7 d. In addition, THP-1 cells were cultured in different levels of Na with and without K. The results showed that salt loading elevated fasting blood glucose, insulin and C-peptide levels, as well as insulin resistance, whereas K supplementation reversed them. Meanwhile, additional K reversed the active effects of high salt on NLRP3 inflammasome in both the subjects and THP-1 cells, and the change of insulin resistance index notably related with the alteration of plasma IL-1 β, the index of NLRP3 inflammasome activation, during intervention in the subjects. Additional K ameliorated oxidative stress induced by high salt in both the subjects and cultured THP-1 cells, and the change of oxidative stress related with the alteration of plasma IL-1 β during intervention in the subjects. In vitro, antioxidant N -acetyl-l -cysteine significantly prevented the active effects of high Na or oxidant Rosup on NLRP3 inflammasome, so did K. Our study indicates that oxidative stress modulation of NLRP3 inflammasome may be involved in the impacts of Na and K on insulin resistance.