Everolimus halts hepatic cystogenesis in a rodent model of polycystic-liver-disease

Temmerman, Frederik;Chen, Feng;Libbrecht, Louis;Vander Elst, Ingrid;van Pelt, Jos;et.al.
(2017) World Journal of Gastroenterology — Vol. 23, n° 30, p. 5499 (2017)

Files

2017_Temmerman_World_J_Gastroenterol.pdf
  • Open Access
  • Adobe PDF
  • 1.55 MB

Details

Authors
  • Temmerman, Frederik
    Author
  • Chen, Feng
    Author
  • Libbrecht, LouisUCLouvain
    Author
  • Vander Elst, Ingrid
    Author
  • van Pelt, Jos
    Author
Show more
Abstract
AIM: To develop a MRI-based method for accurate determination of liver volume (LV) and to explore the effect of long-term everolimus (EVR) treatment on LV in PCK rats with hepatomegaly. METHODS: Thirty-one female PCK rats (model for polycystic-liver-disease: PCLD) were randomized into 3 groups and treatment was started at 16 wk, at the moment of extensive hepatomegaly (comparable to what is done in the human disease). Animals received: controls (n = 14), lanreotide (LAN: 3 mg/kg per 2 wk) (n = 10) or everolimus (EVR: 1 mg/kg per day) (n = 7). LV was measured at week 16, 24, 28. At week 28, all rats were sacrificed and liver tissue was harvested. Fibrosis was evaluated using quantitative image analysis. In addition, gene (quantitative RT-PCR) and protein expression (by Western blot) of the PI3K/AkT/mTOR signaling pathway was investigated. RESULTS: LV determination by MRI correlated excellent with the ex vivo measurements (r = 0.99, P < 0.001). The relative changes in LV at the end of treatment were: (controls) +31.8%; (LAN) +5.1% and (EVR) +8.8%, indicating a significantly halt of LV progression compared with controls (respectively, P = 0.01 and P = 0.04). Furthermore, EVR significantly reduced the amount of liver fibrosis (P = 0.004) thus might also prevent the development of portal hypertension. There was no difference in phosphorylation of Akt (Threonine 308) between LAN-treated PCK rats control PCK rats, whereas S6 was significantly more phosphorylated in the LAN group. Phosphorylation of Akt was not different between controls and EVR treated rats, however, for S6 there was significantly less phosphorylation in the EVR treated rats. Thus, both drugs interact with the PI3K/AkT/mTOR signaling cascade but acting at different molecular levels. CONCLUSION: Everolimus halts cyst growth comparable to lanreotide and reduces the development of fibrosis. mTOR-inhibition should be further explored in PCLD patients especially those that need immunosuppression.
Affiliations

Citations

Temmerman, F., Chen, F., Libbrecht, L., Vander Elst, I., Windmolders, P., Feng, Y., Ni, Y., De Smedt, H., Nevens, F., & van Pelt, J. (2017). Everolimus halts hepatic cystogenesis in a rodent model of polycystic-liver-disease. World Journal of Gastroenterology, 23(30), 5499. https://doi.org/10.3748/wjg.v23.i30.5499 (Original work published 2017)