Martin D G, Watson C E, Gold M B, Woodard C L, Baskin S I
Veterinary Medicine and Laboratory Resources Division, United States Army Medical Research Institute of Chemical Defense, Aberdeen Proving Ground, MD 21010-5425, USA.
J Appl Toxicol. 1995 May-Jun;15(3):153-8. doi: 10.1002/jat.2550150304.
Benzocaine (BNZ) and lidocaine (LC) are commonly used topical (spray) anesthetics approved for use in humans. Benzocaine has structural similarities to methemoglobin (MHb)-forming drugs that are current candidates for cyanide prophylaxis, while LC has been reported to increase MHb in man. In this study, we compared MHb and sulfhemoglobin (SHb) production in three groups of Macaques (Chinese rhesus and Indian rhesus (Macaca mulatta) and pig-tailed macaques (Macaca nemestrina)) after exposure to BNZ and LC. Formation of SHb, unlike MHb, is not thought to be reversible and therefore is considered to be of greater toxic significance. Both MHb and SHb levels were measured periodically on a CO-Oximeter. All rhesus macaques (n = 8) were administered an intratracheal/intranasal) dose of 56 mg (low dose) or 280 mg (high dose) of BNZ or 40 mg of LC in a randomized cross-over design (all animals received all three treatments). Pig-tailed macaques (n = 6) were given an intranasal dose of 56 mg of BNZ and 40 mg of LC. As no differences in the peak MHb or time to peak (mean +/- SD) were observed among the three macaque subspecies, the data were pooled. Lidocaine did not cause MHb or SHb formation above baseline in any monkey. In contrast, all monkeys (n = 14) had a significant elevation in peak MHb formation after 56 mg of BNZ, which ranged from 4.0% to 19.4% with an average of 8.6 +/- 4.0% (mean +/- SD), with peak MHb levels reached at 30 min.(ABSTRACT TRUNCATED AT 250 WORDS)
苯佐卡因(BNZ)和利多卡因(LC)是常用于人类的局部(喷雾)麻醉剂。苯佐卡因与目前作为氰化物预防候选药物的高铁血红蛋白(MHb)形成药物具有结构相似性,而据报道,利多卡因会使人体中的MHb增加。在本研究中,我们比较了三组猕猴(中国恒河猴、印度恒河猴(猕猴)和豚尾猕猴(食蟹猕猴))在接触苯佐卡因和利多卡因后MHb和硫血红蛋白(SHb)的产生情况。与MHb不同,SHb的形成被认为是不可逆的,因此被认为具有更大的毒性意义。通过一氧化碳血氧计定期测量MHb和SHb水平。所有恒河猴(n = 8)采用随机交叉设计,经气管内/鼻内给予56毫克(低剂量)或280毫克(高剂量)的苯佐卡因或40毫克的利多卡因(所有动物接受所有三种治疗)。豚尾猕猴(n = 6)经鼻给予56毫克的苯佐卡因和40毫克的利多卡因。由于在三个猕猴亚种中未观察到峰值MHb或达到峰值的时间(平均值±标准差)存在差异,因此将数据合并。利多卡因在任何猴子中均未导致MHb或SHb形成超过基线水平。相比之下,所有猴子(n = 14)在给予56毫克苯佐卡因后,峰值MHb形成均有显著升高,范围为4.0%至19.4%,平均为(8.6±4.0%)(平均值±标准差),在30分钟时达到峰值MHb水平。(摘要截短为250字)