Berberrubine attenuates potassium oxonate- and hypoxanthine-induced hyperuricemia by regulating urate transporters and JAK2/STAT3 signaling pathway

• DOI: 10.1016/j.ejphar.2021.174592
• Publication Date: 2021-10-25T11:01:39Z
• Authors: Guoshu Lin; Qiuxia Yu; Lieqiang Xu; Ziwei Huang; Liting Mai; Linyun Jiang; Ziren Su; Jianhui Xie; Yucui Li; Yuhong Liu; Zhixiu Lin; Jiannan Chen
• Keywords: Male; Hypoxanthine; 0303 health sciences; Berberine; Glucose Transport Proteins, Facilitative; Organic Anion Transporters; Hyperuricemia; Janus Kinase 2; Organic Anion Transporters, Sodium-Independent; Protective Agents; Blood Urea Nitrogen; 3. Good health; Disease Models, Animal; Mice; Oxonic Acid; 03 medical and health sciences; Organic Anion Transport Protein 1; Creatinine; ATP Binding Cassette Transporter, Subfamily G, Member 2; Animals; Cytokines; Kidney Diseases; Chemical and Drug Induced Liver Injury

Phellodendri Chinensis Cortex (PC) is a traditional medicinal material used to treat gout and hyperuricemia (HUA) in China. Berberine (BBR), the main component of PC, possesses anti-hyperuricemic and anti-gout effects. However, BBR exhibits low bioavailability due to its extensive metabolism and limited absorption. Thus, the metabolites of BBR are believed to be the potential active forms responsible for its in vivo biological activities. Berberrubine (BRB), one of the major metabolites of BBR, exhibits appreciable biological activities even superior to BBR. In this work, the anti-hyperuricemic efficacy of BRB was investigated in HUA model mice induced by co-administration with intraperitoneal potassium oxonate (PO) and oral hypoxanthine (HX) for 7 days. Results showed that administration with BRB (6.25, 12.5, and 25.0 mg/kg) significantly decreased the serum levels of uric acid (UA) by 49.70%, 75.35%, and 75.96% respectively, when compared to the HUA group. In addition, BRB sharply decreased the levels of blood urea nitrogen (BUN) (by 19.62%, 28.98%, and 38.72%, respectively) and serum creatinine (CRE) (by 16.19%, 25.07%, and 52.08%, respectively) and reversed the PO/HX-induced renal histopathological damage dose-dependently. Additionally, BRB lowered the hepatic XOD activity, downregulated the expressions of glucose transporter 9 (GLUT9) and urate transporter 1 (URAT1), upregulated expressions of organic anion transporter 1/3 (OAT1/3) and ATP-binding cassette transporter subfamily G member 2 (ABCG2) at both protein and mRNA levels, and suppressed the activation of the JAK2/STAT3 signaling pathway. In addition, BRB significantly decreased the levels of inflammatory mediators (IL-1β, IL-6, and TNF-α). In conclusion, our study indicated that BRB exerted anti-hyperuricemic effect, at least in part, via regulating the urate transporter expressions and suppressing the JAK2/STAT3 signaling pathway. BRB was believed to be promising for further development into a potential therapeutic agent for HUA treatment.