ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2023 and some content may be unavailable. To unlock all content for 2023, please visit the archives.

Abstract: SA-PO189

Empagliflozin Protects Kidney by Preventing Autophagic Stagnation via Reducing Megalin-Mediated Reabsorption of Lipotoxic Albumin

Session Information

  • AKI: Mechanisms - III
    November 04, 2023 | Location: Exhibit Hall, Pennsylvania Convention Center
    Abstract Time: 10:00 AM - 12:00 PM

Category: Acute Kidney Injury

  • 103 AKI: Mechanisms

Authors

  • Matsui, Sho, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Yamamoto, Takeshi, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Takabatake, Yoshitsugu, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Takahashi, Atsushi, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Namba, Tomoko, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Matsuda, Jun, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Minami, Satoshi, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Sakai, Shinsuke, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Yonishi, Hiroaki, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Nakamura, Jun, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Maeda, Shihomi, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Kawai, Hideaki, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
  • Yanagita, Motoko, Kyoto Daigaku Daigakuin Igaku Kenkyuka Igakubu, Kyoto, Kyoto, Japan
  • Isaka, Yoshitaka, Osaka Daigaku Daigakuin Igakukei Kenkyuka Igakubu, Suita, Osaka, Japan
Background

Evidence from clinical studies such as DAPA-CKD and EMPA-KIDNEY trials suggests that sodium glucose cotransporter 2 (SGLT2) inhibitors confer renal protection regardless of the presence of diabetes, although the underlying mechanisms remain unclear.

Methods

We investigated the following aspects: 1) the impact of empagliflozin (EMPA) on lipotoxicity in kidney proximal tubular epithelial cells (PTECs) in both wildtype and inducible megalin knockout mice, 2) the effect of EMPA on albumin reabsorption in PTECs, 3) the influence of EMPA on autophagic activity, and 4) the effect of EMPA on ischemia-reperfusion injury (IRI) when autophagy and/or megalin are blocked.

Results

High-fat diet (HFD) induced the formation of cytosolic vacuoles (enlarged lysosomes containing phospholipids) in PTECs, which was alleviated by EMPA. Since vacuolar formation was rarely observed in HFD-fed inducible megalin knockout mice, we assessed megalin-mediated fluorescent albumin reabsorption in PTECs. HFD led to hyperreabsorption of albumin in both S1-2 and S3 segments, which was restored by EMPA. Subsequently, we measured plasma levels of 24 fractions of free fatty acids bound to albumin. EMPA improved the imbalanced lipoquality induced by HFD. Furthermore, employing inducible Atg5 knockout mice and GFP-MAP1LC3 transgenic mice, we found that EMPA mitigated the HFD-induced increase in autophagic demand and alleviated the stagnation of autophagy. Finally, we aimed to determine whether the reduced reabsorption of lipotoxic albumin and restoration of autophagic flux by EMPA improve the HFD-induced susceptibility to ischemic stress. The renoprotective effect of empagliflozin against IRI-induced acute kidney injury was attenuated when megalin and/or autophagy were blocked.

Conclusion

The reduction of toxic albumin reabsorption and prevention of autophagic stagnation in PTECs may be crucial for SGLT2 inhibition-mediated renoprotection.

Funding

  • Commercial Support – Japan Boehringer Ingelheim