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作为抗氨噻二唑致畸剂的NAD前体

NAD precursors as antiteratogens against aminothiadiazole.

作者信息

Beaudoin A R

出版信息

Teratology. 1976 Feb;13(1):95-9. doi: 10.1002/tera.1420130114.

Abstract

The teratogen 2-amino-1,3,4-thiadiazole (ATDA) is an antagonist of nicotinamide, and may act by interfering with the synthesis or utilization of the coenzyme nicotinamide adenine dinucleotide (NAD). Several compounds that can be converted to NAD were tested as antiteratogens against ATDA. At day 11 of gestation (sperm day = day 0) pregnant Wistar-derived rats were given single ip injections of ATDA (100 mg/kg), or ATDA immediately followed by the suspected antiteratogen ip or by gavage, or the antiteratogen alone. Compounds tested were NAD, nicotinamide, nicotinic acid, quinolinic acid, kynurenine sulfate, and L-tryptophan, in doses of 10-200 mg per animal. At autopsy (day 20) fetuses were recovered and examined. It was found that each antiteratogen significantly reduced the frequency of ATDA-induced resorptions and malformations. At certain doses each anteteratogen gave complete protection against ATDA-induced malformations in some, but not all, litters. These results support the hypothesis that ADTA interferes with the synthesis or utilization of NAD and suggest that substances converted to NAD act as antiteratogens against ATDA.

摘要

致畸剂2-氨基-1,3,4-噻二唑(ATDA)是烟酰胺的拮抗剂,可能通过干扰辅酶烟酰胺腺嘌呤二核苷酸(NAD)的合成或利用而起作用。几种可转化为NAD的化合物作为抗ATDA致畸剂进行了测试。在妊娠第11天(精子日=第0天),给源自Wistar的怀孕大鼠单次腹腔注射ATDA(100mg/kg),或先注射ATDA,随后立即腹腔注射或灌胃可疑的抗致畸剂,或单独注射抗致畸剂。所测试的化合物有NAD、烟酰胺、烟酸、喹啉酸、硫酸犬尿氨酸和L-色氨酸,每只动物的剂量为10 - 200mg。尸检时(第20天)取出胎儿并进行检查。发现每种抗致畸剂都显著降低了ATDA诱导的吸收和畸形的发生率。在某些剂量下,每种抗致畸剂在部分(但不是全部)窝仔中完全预防了ATDA诱导的畸形。这些结果支持了ADTA干扰NAD合成或利用的假说,并表明可转化为NAD的物质可作为抗ATDA致畸剂。

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