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1,6 - 二氢 - 2 - [2 - (2 - 甲基丙氧基)苯胺基] - 6 - 氧代 - 5 - 嘧啶羧酸对大鼠胃黏膜防御因子及胃分泌的影响

Effect of 1,6-dihydro-2-[2-(2-methylpropoxy)anilino]-6-oxo-5-pyrimidinecarboxylic acid on gastric mucosal defensive factors and gastric secretion in rats.

作者信息

Ishizuka Y, Kamisaki T, Okamoto N, Matsuda M, Shimazaki I, Kimura I, Kamiya A, Kataoka M, Kawashima M, Terashima K

机构信息

Research Laboratories, Roussel Morishita Co., Ltd., Shiga, Japan.

出版信息

Arzneimittelforschung. 1994 May;44(5):620-6.

PMID:8024635
Abstract

1,6-dihydro-2-[2-(2-methylpropoxy)anilino]-6-oxo-5-pyrimidinecarbo xylic acid, (MAR-99, CAS 98772-05-5) (10-30 mg/kg i.g.) improved the reduction of gastric blood flow rate induced by the administration of 99.5% ethanol or acidified-acetylsalicylic acid (ASA). In addition, MAR-99 (3 x 10(-6)-3 x 10(-5) mol/l) protected dose-dependently the damage of epithelial cells induced by ulcerogenic agents such as ethanol or acidified-ASA. MAR-99 (1-10 mg/kg p.o.) prevented dose-dependently the reduction of hexosamine content in glandular stomach. Furthermore, MAR-99 (10-30 mg/kg i.g.) improved the decrease in gastric potential difference induced by 99.5% ethanol and acidified-ASA. MAR-99 (10-30 mg/kg p.o.) significantly inhibited the lesion formation induced by 99.5% ethanol and such effect of this compound was not attenuated by the pretreatment with indomethacin. Furthermore MAR-99 (10 and 30 mg/kg p.o.) had no effect on the prostaglandins (PGE2 and I2) contents in the stomach of normal rats. In pylorus-ligated rats, MAR-99 (3-100 mg/kg i.d.) showed a weak or no effect on acidity and pepsin activity in gastric juice, although this compound decreased dose-dependently the volume of gastric juice. In perfused stomachs, MAR-99 (30-100 mg/kg i.d.) slightly prevented the acid secretion induced by carbachol and pentagastrin. However, MAR-99 did not affect the acid secretion stimulated by histamine. These results indicated that anti-ulcer effect of MAR-99 was mainly due to maintenance of the gastric mucosal resistance.

摘要

1,6 - 二氢 - 2 - [2 - (2 - 甲基丙氧基)苯胺基] - 6 - 氧代 - 5 - 嘧啶羧酸(MAR - 99,化学物质登记号98772 - 05 - 5)(腹腔注射10 - 30毫克/千克)可改善因给予99.5%乙醇或酸化乙酰水杨酸(ASA)所致的胃血流量降低情况。此外,MAR - 99(3×10⁻⁶ - 3×10⁻⁵摩尔/升)可剂量依赖性地保护由乙醇或酸化ASA等致溃疡剂引起的上皮细胞损伤。MAR - 99(口服1 - 10毫克/千克)可剂量依赖性地预防腺胃中氨基己糖含量的降低。此外,MAR - 99(腹腔注射10 - 30毫克/千克)可改善由99.5%乙醇和酸化ASA引起的胃电位差降低。MAR - 99(口服10 - 30毫克/千克)可显著抑制由99.5%乙醇诱导的损伤形成,且吲哚美辛预处理不会减弱该化合物的这种作用。此外,MAR - 99(口服10和30毫克/千克)对正常大鼠胃中前列腺素(PGE₂和I₂)含量无影响。在幽门结扎大鼠中,MAR - 99(十二指肠内注射3 - 100毫克/千克)对胃液酸度和胃蛋白酶活性显示出微弱作用或无作用,尽管该化合物可剂量依赖性地减少胃液体积。在灌注胃中,MAR - 99(十二指肠内注射30 - 100毫克/千克)可轻微预防卡巴胆碱和五肽胃泌素诱导的胃酸分泌。然而,MAR - 99不影响组胺刺激的胃酸分泌。这些结果表明,MAR - 99的抗溃疡作用主要归因于维持胃黏膜抵抗力。

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