研究胡椒基丁醚作为针对肢体和腭部形态发生的音速刺猬通路抑制剂的发育毒性

IF 3.3 4区 医学 Q2 REPRODUCTIVE BIOLOGY Reproductive toxicology Pub Date : 2024-09-08 DOI:10.1016/j.reprotox.2024.108716
Kenneth S. Rivera-González , Porsha M. Reynolds , Robert J. Lipinski
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引用次数: 0

摘要

胡椒基丁醚(PBO)是一种广泛使用的杀虫剂增效剂,人类接触后发现它能抑制音速刺猬(Shh)信号传导,而音速刺猬信号传导是许多发育过程所必需的途径。以前对 PBO 潜在的发育毒性进行的研究得出的结果似乎相互矛盾。我们研究了急性 PBO 暴露对腭和肢体形态发生过程中针对 Shh 通路活性的影响。在妊娠日(GD)9.75时将定时妊娠的C57BL/6 J小鼠暴露于单次PBO剂量(67-1800毫克/千克),在GD10.25和GD10.75时收集仔鼠以检查Shh通路活性,或在GD17时收集仔鼠以进行表型评估。暴露于PBO会诱发剂量依赖性的肢体畸形,最高剂量组会出现腭裂。暴露于PBO后,在胚胎肢芽和颅面过程中观察到Shh通路活性标记物Gli1和Ptch1的表达减少。这些研究结果提供了更多证据,表明产前暴露于以 Shh 通路活性为靶点的 PBO 可导致小鼠畸形,这些畸形与常见的病因复杂的人类先天缺陷相似。
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Examination of piperonyl butoxide developmental toxicity as a Sonic hedgehog pathway inhibitor targeting limb and palate morphogenesis

Piperonyl butoxide (PBO) is a pesticide synergist with widespread use and human exposure that was discovered to inhibit Sonic hedgehog (Shh) signaling, a pathway required for numerous developmental processes. Previous examinations of PBO’s potential for developmental toxicity have generated seemingly conflicting results. We investigated the impact of acute PBO exposure targeting Shh pathway activity during palate and limb morphogenesis. Timed-pregnant C57BL/6 J mice were exposed to a single PBO dose (67–1800 mg/kg) at gestational day (GD) 9.75, and litters were collected at GD10.25 and GD10.75 to examine Shh pathway activity or GD17 for phenotypic assessment. PBO exposure induced dose-dependent limb malformations and cleft palate in the highest dose group. Following PBO exposure, reduced expression of the Shh pathway activity markers Gli1 and Ptch1 was observed in the embryonic limb buds and craniofacial processes. These findings provide additional evidence that prenatal PBO exposure targeting Shh pathway activity can result in malformations in mice that parallel common etiologically complex human birth defects.

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来源期刊
Reproductive toxicology
Reproductive toxicology 生物-毒理学
CiteScore
6.50
自引率
3.00%
发文量
131
审稿时长
45 days
期刊介绍: Drawing from a large number of disciplines, Reproductive Toxicology publishes timely, original research on the influence of chemical and physical agents on reproduction. Written by and for obstetricians, pediatricians, embryologists, teratologists, geneticists, toxicologists, andrologists, and others interested in detecting potential reproductive hazards, the journal is a forum for communication among researchers and practitioners. Articles focus on the application of in vitro, animal and clinical research to the practice of clinical medicine. All aspects of reproduction are within the scope of Reproductive Toxicology, including the formation and maturation of male and female gametes, sexual function, the events surrounding the fusion of gametes and the development of the fertilized ovum, nourishment and transport of the conceptus within the genital tract, implantation, embryogenesis, intrauterine growth, placentation and placental function, parturition, lactation and neonatal survival. Adverse reproductive effects in males will be considered as significant as adverse effects occurring in females. To provide a balanced presentation of approaches, equal emphasis will be given to clinical and animal or in vitro work. Typical end points that will be studied by contributors include infertility, sexual dysfunction, spontaneous abortion, malformations, abnormal histogenesis, stillbirth, intrauterine growth retardation, prematurity, behavioral abnormalities, and perinatal mortality.
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