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局部麻醉药氯普鲁卡因对体细胞杂交的体外诱导作用。

In vitro induction of somatic cell hybridization by the local anesthetic chloroprocaine.

作者信息

Seravalli E P, Lear E, Darlington G J, Cottrell J E

出版信息

Toxicol Appl Pharmacol. 1986 Jul;84(3):628-33. doi: 10.1016/0041-008x(86)90269-3.

Abstract

Chloroprocaine, an aminoester local anesthetic commonly used for epidural block, has been found to induce interspecies somatic cell hybrids in vitro. Mixed cultures of human amniocytes and mouse hepatoma cells, deficient in hypoxanthine phosphoribosyl transferase, were exposed to 1.6, 0.8, or 0.4 X 10(-3)M chloroprocaine for 3 hr at 37 degrees C, then maintained for 3 weeks in a double-selective medium of hypoxanthine, aminopterin, and thymidine (HAT) and ouabain to eliminate the unfused parental cells. Clones of actively multiplying cells appeared in cultures exposed to 1.6 and 0.8 X 10(-3)M chloroprocaine. Chromosome analysis confirmed they were hybrids. Cultures treated with 0.8 X 10(-3)M chloroprocaine exhibited the highest frequency of cell hybridization (8.8 X 10(-5). The hybrid clones bore the morphologic characteristics of both parents although their growth pattern closely resembled the mouse parent. Procaine, sodium bisulfite (the antioxidant present in the commercial solutions of chloroprocaine), and the two chloroprocaine metabolites, chloroaminobenzoic acid and diethylaminoethanol, were nonfusogenic. The hybridogenic effect of chloroprocaine has not been previously described with other local anesthetics.

摘要

氯普鲁卡因是一种常用于硬膜外阻滞的氨基酯类局部麻醉药,已发现在体外可诱导种间体细胞杂交。将缺乏次黄嘌呤磷酸核糖基转移酶的人羊膜细胞和小鼠肝癌细胞混合培养物,在37℃下暴露于1.6、0.8或0.4×10⁻³M氯普鲁卡因中3小时,然后在含有次黄嘌呤、氨基蝶呤和胸腺嘧啶核苷(HAT)以及哇巴因的双重选择培养基中培养3周,以消除未融合的亲本细胞。在暴露于1.6和0.8×10⁻³M氯普鲁卡因的培养物中出现了活跃增殖细胞的克隆。染色体分析证实它们是杂交体。用0.8×10⁻³M氯普鲁卡因处理的培养物表现出最高的细胞杂交频率(8.8×10⁻⁵)。杂交克隆具有双亲的形态学特征,尽管它们的生长模式与小鼠亲本非常相似。普鲁卡因、亚硫酸氢钠(氯普鲁卡因商业溶液中的抗氧化剂)以及两种氯普鲁卡因代谢产物,氯氨基苯甲酸和二乙氨基乙醇,均无融合活性。氯普鲁卡因的杂交生成作用此前尚未在其他局部麻醉药中被描述过。

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