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高铁血红蛋白形成剂对氰化物毒性作用防护效果的比较。

Comparison of methemoglobin formers in protection against the toxic effects of cyanide.

作者信息

Scharf B A, Fricke R F, Baskin S I

机构信息

Division of Drug Assessment, U.S. Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010-5425.

出版信息

Gen Pharmacol. 1992 Jan;23(1):19-25. doi: 10.1016/0306-3623(92)90041-h.

Abstract
  1. Certain compounds that oxidize hemoglobin to methemoglobin (MHb) also protect against cyanide. 2. Evidence presented here suggests that other mechanisms may be involved. 3. Male Swiss ICR mice were pretreated intraperitoneally (i.p.) with various doses of primaquine phosphate (primaquine), WR6026 (6-methoxy-8-(6-diethylamino-hexylamino) lepidine dihydrochloride), WR238605 (8-[(4-amino-1-methylbutyl) amino]-2,6-dimethoxy-4-methyl-5-(3-trifluoromethylphenoxy) quinoline succinate), p-aminooctoyl-phenone (PAOP), or p-aminopropiophenone (PAPP). 4. The compounds were administered 15 or 60 min before an intramuscular (i.m.) challenge with a 2 x LD50 dose (5.0-5.6 mg/kg) of sodium cyanide (NaCN). 5. Twenty-four hr mortality was assessed and survivors were tested for motor incapacitation. 6. Primaquine, PAPP and PAOP increased survival compared to untreated controls, while the other MHb formers were not effective (P less than 0.05). 7. PAOP is believed to form sufficient MHb only after 3 to 4 hr after administration; however it was found to be effective when administered 15 min before NaCN challenge in this study. 8. This suggests that MHb formation may not be the only factor responsible for PAOP's anti-cyanide efficacy.
摘要
  1. 某些将血红蛋白氧化为高铁血红蛋白(MHb)的化合物也能抵御氰化物。2. 此处呈现的证据表明可能涉及其他机制。3. 雄性瑞士ICR小鼠腹腔注射(i.p.)不同剂量的磷酸伯氨喹(伯氨喹)、WR6026(6-甲氧基-8-(6-二乙氨基己基氨基) 勒皮定二盐酸盐)、WR238605(8-[(4-氨基-1-甲基丁基)氨基]-2,6-二甲氧基-4-甲基-5-(3-三氟甲基苯氧基)喹啉琥珀酸盐)、对氨基辛酰苯酮(PAOP)或对氨基丙酰苯酮(PAPP)进行预处理。4. 在肌肉注射(i.m.)2倍半数致死剂量(5.0 - 5.6毫克/千克)的氰化钠(NaCN)进行攻击前15或60分钟给予这些化合物。5. 评估24小时死亡率,对存活小鼠进行运动能力丧失测试。6. 与未处理的对照组相比,伯氨喹、PAPP和PAOP提高了存活率,而其他形成MHb的化合物无效(P小于0.05)。7. 据信PAOP仅在给药后3至4小时才形成足够的MHb;然而在本研究中发现,在NaCN攻击前15分钟给药时它是有效的。8. 这表明MHb的形成可能不是PAOP抗氰化物功效的唯一因素。

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