Molino G, Avagnina P, Torchio M, Garrone M, Fronda G R
Int J Tissue React. 1983;5(3):297-9.
The present study was performed with the aim of establishing whether the muscarinic-receptor antagonist pirenzepine impairs liver blood flow, as previously observed for H2-blockers. For this purpose, two different doses of pirenzepine (0.3 and 0.6 mg/100 g b.w. respectively) were administered to two groups of rats. Liver plasma flow was measured 30 min after treatment by the new sorbitol clearance test which is simple and does not require hepatic vein catheterization. The results were compared with those obtained in a control group and in a group treated with cimetidine. It was shown that, compared to the control group in which the observed functional liver plasma flow was 5.0 +/- 1.3 ml/min/100 g b.w. (MV +/- SD), rats treated with either dose of pirenzepine showed no significant impairment of liver perfusion. On the other hand, cimetidine treatment produced a significant reduction (p less than 0.001) of functional liver plasma flow. Our results show that pirenzepine treatment does not significantly impair liver functional activity through reduced liver perfusion. They also suggest that muscarinic receptors are probably not involved in the control of splanchnic blood flow.
本研究旨在确定毒蕈碱受体拮抗剂哌仑西平是否会像先前观察到的H2阻滞剂那样损害肝血流量。为此,将两组大鼠分别给予两种不同剂量的哌仑西平(分别为0.3和0.6 mg/100 g体重)。治疗30分钟后,通过新的山梨醇清除试验测量肝血浆流量,该试验简单且无需肝静脉插管。将结果与对照组和用西咪替丁治疗的组获得的结果进行比较。结果表明,与观察到功能性肝血浆流量为5.0±1.3 ml/min/100 g体重(平均值±标准差)的对照组相比,用任何一种剂量哌仑西平治疗的大鼠肝灌注均未出现明显损害。另一方面,西咪替丁治疗导致功能性肝血浆流量显著降低(p<0.001)。我们的结果表明,哌仑西平治疗不会通过降低肝灌注而显著损害肝功能活动。它们还表明,毒蕈碱受体可能不参与内脏血流量的控制。