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首页> 外文期刊>Japanese Journal of Pharmacology >EFFECTS OF 1-MORPHOLINOACETYL-2-METHYL-3-PHENYL-4-OXO-1, 2, 3, 4-TETRAHYDRO QUINAZOLINE HYDROCHLORIDE (HQ-275) ON α-NAPHTYL ISOTHIO-CYANATE- AND/OR THIOACETAMIDE-INDUCED LIVER DAMAGE IN RATS
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EFFECTS OF 1-MORPHOLINOACETYL-2-METHYL-3-PHENYL-4-OXO-1, 2, 3, 4-TETRAHYDRO QUINAZOLINE HYDROCHLORIDE (HQ-275) ON α-NAPHTYL ISOTHIO-CYANATE- AND/OR THIOACETAMIDE-INDUCED LIVER DAMAGE IN RATS

机译:1-吗啉代乙酰基-2-甲基-3-苯基-4-OXO-1、2、3、4-四氢喹唑啉盐酸盐(HQ-275)对α-萘异氰酸酯和/或硫代乙酰胺诱导的肝损伤的影响在大鼠

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References(19) Pharmacological properties of 1-morpholinoacetyl-2-methyl-3-phenyl-4oxo-1, 2, 3, 4-tetrahydro quinazoline hydrochloride (HQ-275), which has a potent choleretic activity, on ANIT and TAA-hepatic injury have been investigated in rats for biochemical, histochemical levels and the functions in the liver. Regarding the actions of biliary and solid content excretion, HQ-275 demonstrates differences between normal rats and the groups administered ANIT and/or TAA, and also the lowered values of Al-P, transaminases and bilirubin in plasma, elevated by the ANITpoisoning. Thus a comparable effect of HQ-275 against TAA-poisoning was not observed. TAA-induced elevation of the plasma-lipid level was significantly prevented by the administration of HQ-275. Moreover, under light microscopical examination, the decrease of 5'-N by the ANIT-poisoning was prevented even with small doses of HQ-275 3-6 mg/kg, p.o. Elevation of the cholesterol level in plasma and decrease of ATP-ase in histochemical findings by ANIT-intoxication were not in themselves recognizable. Changes of Na+ and K+ in bile and water content of liver by poisoning of ANIT were clearly prevented with HQ-275. On the other hand, HQ-275 revealed no effects on the actions produced by TAA-intoxication except for those mentioned. Such being the case it can be concluded that HQ-275 inhibits the ANIT-induced hepatic injury to a greater extent than the TAA-induced hepatic damage for biochemical and histochemical levels.
机译:参考文献(19)1-吗啉代乙酰基-2-甲基-3-苯基-4氧代-1、2、3、4-四氢喹唑啉盐酸盐(HQ-275)对ANIT和TAA-的药理特性已经研究了大鼠肝损伤的生化,组织化学水平和肝脏功能。关于胆汁和固形物排泄的作用,HQ-275证明正常大鼠与ANIT和/或TAA给药组之间存在差异,并且由于ANIT中毒导致血浆中的Al-P,转氨酶和胆红素值降低。因此,未观察到HQ-275对TAA中毒的可比作用。施用HQ-275可显着防止TAA诱导的血浆脂质水平升高。此外,在光学显微镜检查下,即使使用小剂量的HQ-275 3-6 mg / kg,p.o,也可以防止由于ANIT中毒而导致的5'-N降低。自身无法识别血浆中胆固醇水平的升高和ANIT中毒后组织化学结果中ATP酶的降低。 HQ-275明显防止了ANIT中毒导致胆汁中Na +和K +的变化以及肝中水分的变化。另一方面,HQ-275除了提到的那些外,没有显示出对TAA醉毒产生的作用的影响。在这种情况下,可以得出结论,就生化和组织化学水平而言,与TAA诱导的肝损伤相比,HQ-275在更大程度上抑制了ANIT诱导的肝损伤。

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