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首页> 外文期刊>British Journal of Pharmacology >Effects of specific inhibition of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the rat stomach with normal mucosa and after acid challenge
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Effects of specific inhibition of cyclo-oxygenase-1 and cyclo-oxygenase-2 in the rat stomach with normal mucosa and after acid challenge

机译:正常粘膜和酸刺激后对大鼠胃中环氧合酶-1和环氧合酶-2的特异性抑制作用

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摘要

Effects of the cyclo-oxygenase(COX)-1 inhibitor SC-560 and the COX-2 inhibitors rofecoxib and DFU were investigated in the normal stomach and after acid challenge. In healthy rats, neither SC-560 nor rofecoxib(20 mg kg~-1 each)given alone damaged the Mucosa. Co-treatment with SC-560 and rofecoxib, however, induced severe lesions comaprable to Indomethacin(20 mg kg~-1)whereas co-administration of SC-560 and DFU(20 mg kg~-1 each)had No comparable ulcerogenic effect 5 after dosing. SC-560(20 mg kg~-1)inhibited gastric 6-keto-prostaglandin(PG)F_1αby 86±5/100 and platelet Thromboxane(TX)B_2 formation by 89±4/100 comparable to indomethacin(20 mg kg~-1).
机译:在正常胃和酸刺激后,研究了环加氧酶(COX)-1抑制剂SC-560和COX-2抑制剂rofecoxib和DFU的作用。在健康大鼠中,单独给予SC-560和罗非考昔(各自20 mg kg〜-1)均不会损害粘膜。然而,SC-560和罗非考昔的联合治疗可引起严重的病灶,可与吲哚美辛(20 mg kg〜-1)共同映射,而SC-560和DFU(20 mg kg〜-1)的共同给药没有类似的致溃疡作用给药后5。与吲哚美辛(20 mg kg〜-)相比,SC-560(20 mg kg〜-1)抑制胃6-酮-前列腺素(PG)F_1α的作用为86±5/100,而血小板血栓烷(TX)B_2的形成为89±4/100。 1)。

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