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多氯联苯(酚氯和派腊纶)与小鼠体内己糖和氨基酸的肠道转运

Polychlorinated biphenyls (phenoclor and pyralene) and intestinal transport of hexoses and amino acids in mice.

作者信息

Madge D S

出版信息

Gen Pharmacol. 1976 Sep;7(4):249-54. doi: 10.1016/0306-3623(76)90083-5.

Abstract
  1. Using mouse everted whole small intestine 7 days after a single dose of Phenoclor DP6 (hexachlorobiphenyl) at 1.0 g kg-1 body wt, absorption of D-glucose decreased significantly, probably owing to toxic traces of pentodicholobenzofuran in the PCB preparation and not its high chlorine content. D-glucose tissue accumulation decreased. The serosal fluid transfer also fell but not the gut fluid uptake. D-glucose absorption and fluid transfer remained unchanged following doses of other Phenoclor and Pyralene (PCB) compounds. 2. Using DP6, malabsorption of D-glucose and impaired serosal fluid transfer were not evident 7 days after a single dose of 0.1, 0.25 and 0.50 g kg-1 body wt. One to 21 days after a single dose (1.0 g kg-1 body wt) of DP6, D-glucose absorption and serosal fluid transfer decreased from 3 to 14 days but thereafter became normal. 3. Although absorption of D-galactose, D-glucose following membrane hydrolysis of D-maltose, and L-arginine, L-histidine, L-ornithine and L-proline decreased slightly 7 days after a single dose of Phenoclor DP6,the results were not significant, nor were changes in fluid transfer. 4. Following Phenoclor DP6-treatment, D-glucose malabsorption was abolished by an exogenous energy supply (D-mannose). DP6 affected intracellular metabolism and not the glucose carrier at the membrane brush border. 5. The body-weights and fresh small intestinal weights of mice treated with different PCBs remained unchanged after seven days. The histology of the small intestine showed minimal changes.
摘要
  1. 给小鼠单剂量腹腔注射1.0 g/kg体重的二氯二苯并呋喃(Phenoclor DP6,六氯联苯)7天后,使用外翻的完整小肠进行实验,结果显示D-葡萄糖的吸收显著下降,这可能是由于多氯联苯制剂中含有痕量有毒的五氯二苯并呋喃,而非其高氯含量所致。D-葡萄糖在组织中的蓄积量减少。浆膜液转移量也下降,但肠液摄取量未变。给予其他二氯二苯并呋喃和多氯联苯(PCB)化合物后,D-葡萄糖的吸收和液体转移未发生变化。2. 单剂量给予0.1、0.25和0.50 g/kg体重的Phenoclor DP6 7天后,未观察到D-葡萄糖吸收不良和浆膜液转移受损的情况。单剂量给予1.0 g/kg体重的Phenoclor DP6后1至21天,D-葡萄糖吸收和浆膜液转移在第3至14天下降,但此后恢复正常。3. 单剂量给予Phenoclor DP6 7天后,尽管D-半乳糖、D-麦芽糖经膜水解后的D-葡萄糖、L-精氨酸、L-组氨酸、L-鸟氨酸和L-脯氨酸的吸收略有下降,但结果并不显著,液体转移也未发生变化。4. 经Phenoclor DP6处理后,外源性能量供应(D-甘露糖)可消除D-葡萄糖吸收不良的现象。Phenoclor DP6影响细胞内代谢,而非膜刷状缘的葡萄糖载体。5. 用不同多氯联苯处理的小鼠体重和新鲜小肠重量在7天后保持不变。小肠组织学变化极小。

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