Kurihara T, Akimoto M, Kurokawa K, Ishiguro H, Niimi A, Maeda A, Sigemoto M, Yamashita K, Yokoyama I, Hirayama Y
Institute of Geriatrics, Tokyo Women's Medical College, Japan.
Life Sci. 1992;51(26):PL281-5. doi: 10.1016/0024-3205(92)90166-m.
In our previous study, we determined changes in hepatic blood flow using a Laser Doppler blood flow meter after i.v. injection of endothelin-1 (ET-1) or endothelin-3 (ET-3) at 2 nmol/kg in rats and found that ET-3 caused greater decreases in blood flow than ET-1. In the present study, we determined how the arachidonic acid cascade, mainly thromboxane A2 (TXA2), is related to ET-1 and ET-3 using indomethacin (INDO), which inhibits the biosynthesis of prostaglandin (PG), and OKY-046, a selective inhibitor of TXA2 synthesis. In the first series of experiments, ET-1 and ET-3 were administered after inhibiting the biosynthesis of PG by s.c. injection of 2 mg/kg of INDO. While INDO failed to inhibit the slight decrease in hepatic blood flow induced by ET-1, it significantly inhibited the marked decrease in hepatic blood flow elicited by ET-3. In the next series of experiments, ET-1 and ET-3 were administered after administration of 20 mg/kg of OKY-046. OKY-046 showed no effects in animals treated with ET-1, as in those pre-treated with INDO, while it significantly inhibited the decreases in hepatic blood flow induced by ET-3. These findings suggest that ET-1 decreases hepatic blood flow due to its direct effects although to a lesser extent than ET-3, while ET-3 does so due not only to its direct effects but also to TXA2-mediated effects. It is therefore likely that in addition to ET family peptides, PG-mediated mechanisms are involved in the regulation of hepatic microcirculation by ETs.
在我们之前的研究中,我们在大鼠静脉注射2 nmol/kg内皮素-1(ET-1)或内皮素-3(ET-3)后,使用激光多普勒血流仪测定肝血流量的变化,发现ET-3引起的血流量下降比ET-1更大。在本研究中,我们使用抑制前列腺素(PG)生物合成的吲哚美辛(INDO)和血栓素A2(TXA2)合成的选择性抑制剂OKY-046,确定花生四烯酸级联反应(主要是TXA2)与ET-1和ET-3之间的关系。在第一系列实验中,通过皮下注射2 mg/kg的INDO抑制PG生物合成后,给予ET-1和ET-3。虽然INDO未能抑制ET-1诱导的肝血流量轻微下降,但它显著抑制了ET-3引起的肝血流量显著下降。在下一系列实验中,给予20 mg/kg的OKY-046后,再给予ET-1和ET-3。与用INDO预处理的动物一样,OKY-046对用ET-1处理的动物没有影响,而它显著抑制了ET-3诱导的肝血流量下降。这些发现表明,ET-1通过其直接作用降低肝血流量,尽管程度比ET-3小,而ET-3不仅通过其直接作用,还通过TXA2介导的作用降低肝血流量。因此,除了ET家族肽外,PG介导的机制可能也参与了ETs对肝微循环的调节。