Suppr超能文献

新生动物的药物处置,特别涉及马驹。

Drug disposition in the neonatal animal, with particular reference to the foal.

作者信息

Baggot J D, Short C R

出版信息

Equine Vet J. 1984 Jul;16(4):364-7. doi: 10.1111/j.2042-3306.1984.tb01945.x.

Abstract

Differences between neonatal and adult animals in their response to drugs can usually be attributed to altered disposition (ie, distribution, metabolism and excretion) processes during the neonatal period. These alterations affect the plasma concentrations as well as the concentrations of drug attained at the receptor site. Some characteristics of the neonatal period include greater absorption from the gastrointestinal tract, lower extent of plasma protein binding, increased apparent volume of distribution of drugs that distribute in extracellular fluid or total body water, increased permeability of the 'blood-brain' barrier and slower elimination of many drugs. The hepatic microsomal oxidative reactions and glucuronide conjugation are deficient metabolic pathways for a varying period of time, usually up to six weeks after birth or even longer in some species. Decreased metabolism can affect the duration of action of lipid-soluble drugs. Functional immaturity of the kidneys decreases the renal excretion of polar drugs and drug metabolites. Overall renal function appears to reach maturity within two weeks after birth in ruminant species and pigs, while maturation may take at least four weeks in other species of domestic animals. Considerable physiological and biochemical development takes place during the first five days after birth with maturation continuing more slowly over the succeeding five weeks. The time it takes for any process to reach functional maturity depends on the process in question and varies with the species of animal. The absorption, disposition and pharmacological response to drugs during the first 24 h after birth may be unique to that time and, because of lack of information, are impossible to predict.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

新生动物与成年动物对药物反应的差异通常可归因于新生儿期处置过程(即分布、代谢和排泄)的改变。这些改变会影响血浆浓度以及药物在受体部位达到的浓度。新生儿期的一些特征包括胃肠道吸收增加、血浆蛋白结合程度降低、分布于细胞外液或全身水中的药物表观分布容积增加、“血脑”屏障通透性增加以及许多药物消除缓慢。肝微粒体氧化反应和葡萄糖醛酸结合在一段不同的时间内是缺乏的代谢途径,通常在出生后长达六周,在某些物种中甚至更长。代谢降低会影响脂溶性药物的作用持续时间。肾脏功能不成熟会降低极性药物和药物代谢物的肾排泄。反刍动物和猪的总体肾功能在出生后两周内似乎达到成熟,而其他家畜物种的成熟可能至少需要四周。出生后的头五天会发生相当大的生理和生化发育,随后的五周内成熟过程继续缓慢进行。任何过程达到功能成熟所需的时间取决于所讨论的过程,并因动物物种而异。出生后最初24小时内对药物的吸收、处置和药理反应可能在那个时期是独特的,并且由于缺乏信息,无法预测。(摘要截断于250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验