Diewert V M
Teratology. 1981 Aug;24(1):43-52. doi: 10.1002/tera.1420240106.
The lathyrogen beta-aminoproprionitrile (BAPN) induces cleft palate in rats when administered at a critical time in secondary palate formation. BAPN is known to inhibit the crosslinking of newly synthesized collagen, but its primary site of action in producing cleft palate is unknown. In this study time-mated Sprague-Dawley rats were given a single oral dose of 600 mg/kg BAPN at five known gestational ages in the 48 hours before palatal shelf elevation, and the fetuses were studied on days 16, 17 and 18. Evaluation of craniofacial relations and palate development in BAPN-treated heads revealed that delayed palatal shelf elevation and resulting cleft palate were related to retrognathia of the mandible. However, shortening of the mandible was due primarily to vertical and lateral bending of Meckel's cartilage. High and retruded tongue positions that were present with the deformities in Meckel's cartilage interfered with palatal shelf movement to the horizontal plane. The group treated with BAPN at 15 days 7 hours, approximately 24 hours before normal palatal shelf elevation, had the most severe defects in Meckel's cartilage, the longest delay in palatal shelf elevation and the highest incidence of cleft palate. Inhibition of crosslinking of collagen in Meckel's cartilage appeared to weaken the cartilage during the critical period in facial development when extention of the tongue and mandible beneath the primary palate is required to facilitate palatal shelf elevation.
致畸形物β-氨基丙腈(BAPN)在大鼠次生腭形成的关键时期给药时会诱发腭裂。已知BAPN会抑制新合成胶原蛋白的交联,但其导致腭裂的主要作用部位尚不清楚。在本研究中,在腭架抬高前48小时的五个已知妊娠阶段,对同期交配的斯普拉格-道利大鼠单次口服600mg/kg BAPN,并在第16、17和18天对胎儿进行研究。对经BAPN处理的头部的颅面关系和腭部发育评估显示,腭架抬高延迟和由此导致的腭裂与下颌后缩有关。然而,下颌缩短主要是由于梅克尔软骨的垂直和侧向弯曲。梅克尔软骨畸形时出现的高而回缩的舌位干扰了腭架向水平面的移动。在正常腭架抬高前约24小时的第15天7小时用BAPN处理的组,梅克尔软骨的缺陷最严重,腭架抬高延迟最长,腭裂发生率最高。在面部发育的关键时期,当需要在原发腭下方伸展舌头和下颌以促进腭架抬高时,抑制梅克尔软骨中胶原蛋白的交联似乎会削弱软骨。