4.7 Article

Juglanin protects against high fat diet-induced renal injury by suppressing inflammation and dyslipidemia via regulating NF-κB/HDAC3 signaling

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 95, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.intimp.2020.107340

Keywords

Renal injury; Juglanin; Lipid accumulation; Inflammation; NF-kappa B/HDAC3

Funding

  1. National Natural Science Foundation of China [81703527]
  2. Chongqing Research Program of Basic Research and Frontier Technology [cstc2017jcyjAX0356, cstc2018jcyjAX0393, cstc2018jcyjAX0811, cstc2018jcyjA3533]
  3. Science and Technology Research Program of Chongqing Municipal Education Commission [KJZDM201801601]
  4. Children's Research Institute of National Center for Schooling Development Programme [CRIKT201908]
  5. Chongqing University of Education [CRIKT201908]
  6. Chongqing Professional Talents Plan for Innovation and Entrepreneurship Demonstration Team [CQCY201903258]

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The study showed that Jug could alleviate obesity-induced renal injury by suppressing the nuclear translocation of NF-kappa B and HDAC3, thus reducing inflammation and lipid accumulation, ultimately improving kidney function.
Obesity is an important factor implicated in chronic kidney disease (CKD). Juglanin (Jug) is a natural compound extracted from the crude Polygonumaviculare, showing anti-inflammatory and anti-diabetic effects. However, whether Jug has protective effects against obesity-induced renal injury, little has been investigated. Herein, we attempted to explore the potential of Jug in mediating obesity-induced kidney disease in high fat diet (HFD)challenged mice. Our results suggested that chronic HFD feeding markedly increased the body weights of mice compared to the ones fed with normal chow diet (NCD), along with significant glucose intolerance and insulin resistance. However, these metabolic disorders induced by HFD were effectively alleviated by Jug treatments in a dose-dependent manner. Moreover, HFD-challenged mice showed apparent histopathological changes in renal tissues with significant collagen accumulation, which were attenuated by Jug supplementation. In addition, Jug treatment decreased the expression levels of kidney injury molecule-1 (KIM-1), while increased nephrin and podocin expression levels in kidney of HFD-challenged mice, improving the renal dysfunction. Furthermore, HFD led to lipid deposition in kidney samples of mice by enhancing abnormal lipid metabolism. In addition, HFD promoted the releases of circulating pro-inflammatory cytokines, and enhanced the renal inflammation by activating nuclear factor-kappa B/histone deacetylase 3 (NF-kappa B/HDAC3) signaling. HFD-induced dyslipidemia and inflammation were considerably abrogated by Jug administration in mice. The protective effects of Jug against renal injury were confirmed in palmitate (PA)-stimulated HK2 cells in vitro mainly through suppressing the nuclear translocation of NF-kappa B and HDAC3, repressing inflammation and lipid accumulation eventually. Hence, Jug could ameliorate HFD-induced kidney injury mainly through blocking the NF-kappa B/HDAC3 nuclear translocation.

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