Frederik Temmerman, Ingrid Vander Elst, Petra Windmolders, Frederik Nevens, Jos van Pelt, Laboratory of Hepatology, Department of Clinical and Experimental Medicine, Faculty of Medicine, University of Leuven, B 3000 Leuven, Belgium.
World J Gastroenterol. 2017 Aug 14;23(30):5499-5507. doi: 10.3748/wjg.v23.i30.5499.
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.
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 ( = 14), lanreotide (LAN: 3 mg/kg per 2 wk) ( = 10) or everolimus (EVR: 1 mg/kg per day) ( = 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.
LV determination by MRI correlated excellent with the measurements ( = 0.99, < 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, = 0.01 and = 0.04). Furthermore, EVR significantly reduced the amount of liver fibrosis ( = 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 was significantly more phosphorylated in the LAN group. Phosphorylation of Akt was not different between controls and EVR treated rats, however, for 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.
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.
开发一种基于 MRI 的方法来准确测定肝体积(LV),并探讨长期依维莫司(EVR)治疗对多囊肝病(PCLD)大鼠肝肿大模型 LV 的影响。
31 只雌性 PCK 大鼠(多囊肝病模型)被随机分为 3 组,在 16 周时开始治疗,此时出现广泛肝肿大(与人类疾病相同)。动物接受:对照组(n = 14)、兰瑞肽(LAN:每 2 周 3mg/kg)(n = 10)或依维莫司(EVR:每天 1mg/kg)(n = 7)。在第 16、24、28 周时测量 LV。第 28 周时,所有大鼠被处死并采集肝脏组织。使用定量图像分析评估纤维化。此外,还通过定量 RT-PCR 和 Western blot 检测 PI3K/AkT/mTOR 信号通路的基因(定量 RT-PCR)和蛋白表达(Western blot)。
MRI 测定的 LV 与测量值相关性极好(r = 0.99,P < 0.001)。治疗结束时 LV 的相对变化为:(对照组)+31.8%;(LAN)+5.1%和(EVR)+8.8%,与对照组相比,LV 进展明显减慢(分别为 P = 0.01 和 P = 0.04)。此外,EVR 显著减少了肝纤维化的程度(P = 0.004),因此可能也预防了门静脉高压的发展。LAN 治疗的 PCK 大鼠与对照组 PCK 大鼠的 Akt(苏氨酸 308 位)磷酸化无差异,而 LAN 组的磷酸化明显增加。EVR 治疗组与对照组之间的 Akt 磷酸化无差异,但 EVR 治疗组的磷酸化明显减少。因此,两种药物均与 PI3K/AkT/mTOR 信号级联相互作用,但作用于不同的分子水平。
依维莫司能阻止囊肿生长,效果与兰瑞肽相当,并能减少纤维化的发展。mTOR 抑制剂应在 PCLD 患者中进一步探索,特别是需要免疫抑制的患者。