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[Cytogenetic studies of human lymphocytes under the influence of oxicams].
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本文引用的文献

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Prevention of the gastrotoxicity of aspirin and related drugs in rats by lithium salts and sodium thiocyanate.锂盐和硫氰酸钠对大鼠阿司匹林及相关药物胃毒性的预防作用
Toxicol Appl Pharmacol. 1983 Apr;68(2):323-7. doi: 10.1016/0041-008x(83)90016-9.
2
Isoxicam.异恶酰草胺
Clin Rheum Dis. 1984 Aug;10(2):385-99.
3
Interleukin-1 and the pathogenesis of the acute-phase response.白细胞介素-1与急性期反应的发病机制。
N Engl J Med. 1984 Nov 29;311(22):1413-8. doi: 10.1056/NEJM198411293112205.
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Effects of model traumatic injury on hepatic drug metabolism in the rat. I. In vivo antipyrine metabolism.
Drug Metab Dispos. 1983 Nov-Dec;11(6):517-25.
5
Esterification of acidic anti-inflammatory drugs suppresses their gastrotoxicity without adversely affecting their anti-inflammatory activity in rats.酸性抗炎药物的酯化作用可抑制其对大鼠的胃毒性,且不会对其抗炎活性产生不利影响。
J Pharm Pharmacol. 1980 Nov;32(11):795-6. doi: 10.1111/j.2042-7158.1980.tb13073.x.
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Impaired drug metabolism in rats associated with acute inflammation: a possible assay for anti-injury agents.
Proc Soc Exp Biol Med. 1974 Jan;145(1):135-40. doi: 10.3181/00379727-145-37763.
7
Preliminary investigations on the pharmacological control of catabolin-induced cartilage destruction in vitro.关于体外药理控制分解代谢素诱导的软骨破坏的初步研究。
Agents Actions. 1985 Mar;16(1-2):55-7. doi: 10.1007/BF01999648.
8
Experience with isoxicam and catabolin.异恶酰胺与卡他步林的使用经验。
Br J Clin Pharmacol. 1986;22 Suppl 2(Suppl 2):121S-124S. doi: 10.1111/j.1365-2125.1986.tb02992.x.
9
Temporal pattern and reversal of impaired hepatic mono-oxygenases by phenobarbital in rats with developing and established adjuvant disease.苯巴比妥对患有正在发展和已确诊佐剂病大鼠肝脏单加氧酶受损的时间模式及逆转作用
J Pharmacol Exp Ther. 1977 Oct;203(1):169-83.
10
Non-steroid anti-inflammatory drugs: combined assay for anti-edemic potency and gastric ulcerogenesis in the same animal.非甾体抗炎药:在同一动物中进行抗水肿效力和胃溃疡形成的联合测定。
Life Sci. 1977 Aug 1;21(3):371-7. doi: 10.1016/0024-3205(77)90517-3.

昔康类药物:大鼠体内的相对安全性及抗损伤作用

Oxicams: relative safety and anti-injury effects in rats.

作者信息

Whitehouse M W

出版信息

Br J Clin Pharmacol. 1986;22 Suppl 2(Suppl 2):111S-116S. doi: 10.1111/j.1365-2125.1986.tb02990.x.

DOI:10.1111/j.1365-2125.1986.tb02990.x
PMID:3497658
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1400958/
Abstract

1 Oxicams have certain distinctive properties, which distinguish them from other arylalkanoic (carboxylic) acids that show anti-inflammatory/analgesic/antipyretic activities. These include: (i) slow rates of metabolism (ii) lesser gastro-irritancy/ulcerogenicity (iii) preventing fever development (iv) some effect on the adaptive responses of the liver to severe inflammation or trauma that compromise normal hormone/xenobiotic metabolism (detoxification). 2 Isoxicam was notably less gastrotoxic than either piroxicam or tenoxicam, when given either orally or parenterally, at equipotent doses in rats.

摘要
  1. 昔康类药物具有某些独特的性质,这使其有别于其他具有抗炎/镇痛/解热活性的芳基链烷酸(羧酸)。这些特性包括:(i)代谢速率缓慢;(ii)胃肠道刺激性/致溃疡作用较小;(iii)预防发热;(iv)对肝脏针对严重炎症或创伤的适应性反应有一定影响,而这种炎症或创伤会损害正常的激素/外源性物质代谢(解毒)。2. 在大鼠中,给予等剂量的异恶酰胺,无论是口服还是肠胃外给药,其胃肠道毒性均明显低于吡罗昔康或替诺昔康。