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用兔角膜上皮细胞原代培养物评估丁卡因、丙美卡因和可卡因的比较毒性。

Comparative toxicity of tetracaine, proparacaine and cocaine evaluated with primary cultures of rabbit corneal epithelial cells.

作者信息

Grant R L, Acosta D

机构信息

Department of Pharmacology/Toxicology, College of Pharmacy, University of Texas at Austin 78712.

出版信息

Exp Eye Res. 1994 Apr;58(4):469-78. doi: 10.1006/exer.1994.1040.

Abstract

Cocaine was first used as a topical anesthetic for the eye by Dr Carl Koller in 1884. It became evident that this agent produced erosion of the corneal epithelium in high doses or with repeated use. Synthetic local anesthetics such as tetracaine and proparacaine were developed which were more potent and less toxic than cocaine, but still produced corneal epithelium defects if used chronically. This investigation was undertaken to compare and rank the cytotoxicity of the most commonly used ocular local anesthetics, tetracaine, proparacaine and cocaine, with primary cultures of rabbit corneal epithelial cells. Cultures were exposed to either low concentrations of local anesthetics for 4-24 hr or to higher concentrations of local anesthetics for 15-120 min. Plasma membrane integrity was evaluated by measuring leakage of the cytosolic enzyme, lactate dehydrogenase, into the medium. Cell shape changes were evaluated by observing morphological changes. Mitochondrial dehydrogenase activity and cell viability were assessed by measuring 3-(4,5-dimethythiazol-2yl)-2,5-diphenyl tetrazolium bromide reduction. The cytotoxicity of the local anesthetics as evaluated by the lactate dehydrogenase leakage cytotoxicity test was ranked as follows: tetracaine (EC50 = 0.96 mM) >> proparacaine (EC50 = 4.4 mM) > cocaine (EC50 = 9.7 mM). The mitochondrial reduction assay seemed to be more sensitive than the lactate dehydrogenase leakage test in predicting toxicity: tetracaine (EC50 = 0.81 mM) >> proparacaine (EC50 = 3.4 mM) > cocaine (EC50 = 7.1 mM). When corneal epithelial cells were treated with local anesthetics, marked morphological changes occurred at concentrations that did not cause a decrease in viability. This was especially true for cocaine-treated cells. Tetracaine and proparacaine have the same anesthetic potency in vivo, although tetracaine is considered to be more irritating than proparacaine. This in vitro study showed that tetracaine was approximately four times more toxic than proparacaine. Cocaine was less toxic in vitro than proparacaine and tetracaine when compared on an equimolar basis, but in vivo it may be more toxic because of the higher concentrations that must be used to obtain the same degree of anesthesia as well as its marked effects on cell morphology.

摘要

1884年,卡尔·科勒医生首次将可卡因用作眼部局部麻醉剂。显然,高剂量使用或反复使用该药物会导致角膜上皮糜烂。后来研发出了丁卡因和丙美卡因等合成局部麻醉剂,它们比可卡因效力更强、毒性更小,但长期使用仍会导致角膜上皮缺损。本研究旨在比较最常用的眼部局部麻醉剂丁卡因、丙美卡因和可卡因对兔角膜上皮细胞原代培养物的细胞毒性并进行排名。培养物分别暴露于低浓度局部麻醉剂4至24小时或高浓度局部麻醉剂15至120分钟。通过测量胞质酶乳酸脱氢酶泄漏到培养基中的情况来评估质膜完整性。通过观察形态变化来评估细胞形状改变。通过测量3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑的还原情况来评估线粒体脱氢酶活性和细胞活力。通过乳酸脱氢酶泄漏细胞毒性试验评估的局部麻醉剂细胞毒性排名如下:丁卡因(半数有效浓度[EC50]=0.96毫摩尔)>>丙美卡因(EC50=4.4毫摩尔)>可卡因(EC50=9.7毫摩尔)。线粒体还原试验在预测毒性方面似乎比乳酸脱氢酶泄漏试验更敏感:丁卡因(EC50=0.81毫摩尔)>>丙美卡因(EC50=3.4毫摩尔)>可卡因(EC50=7.1毫摩尔)。当用局部麻醉剂处理角膜上皮细胞时,在不会导致活力下降的浓度下就会出现明显的形态变化。可卡因处理的细胞尤其如此。丁卡因和丙美卡因在体内具有相同的麻醉效力,尽管丁卡因被认为比丙美卡因更具刺激性。这项体外研究表明,丁卡因的毒性约为丙美卡因的四倍。在等摩尔基础上比较时,可卡因在体外的毒性低于丙美卡因和丁卡因,但在体内可能毒性更大,因为要获得相同程度的麻醉必须使用更高的浓度,以及它对细胞形态有显著影响。

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