Ibrahim Khalid Elfakki, Khan Haseeb Ahmad, Omer Fayza Ahmad
Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
Department of Biochemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
Exp Toxicol Pathol. 2014 Mar;66(2-3):89-96. doi: 10.1016/j.etp.2013.11.004. Epub 2013 Dec 12.
Iminodipropionitrile (IDPN) is a prototype nitrile compound that produces excitation, chorea and circling (ECC) syndrome in rodents. Previous studies have implicated vestibular hair cell degeneration in IDPN-induced behavioral abnormalities. Although the pathological changes in vestibular labyrinth of IDPN-treated rats are well documented, the effects of IDPN on other organ systems are not clearly understood. We therefore examined the histopathological alterations in inner ear, brain, liver and kidneys of rats exposed to IDPN. Adult male Wistar rats were divided into two groups of six animals each. Control rats received normal saline whereas the IDPN group was treated with IDPN (100mg/kg, i.p.) daily for 7 days. All the animals were carefully observed for any behavioral abnormality and the dyskinetic movements including the vertical and horizontal head weaving, circling and backward walking were quantified. The animals were sacrificed on day 9 and the samples of cochlea, brain, liver and kidney were collected for histopathology. The results showed a direct correlation between the severity of behavioral deficits and the cellular damage in crista ampullaris in IDPN-treated rats. Histopathology of liver was severely influenced by IDPN treatment, leading to vacuolization of cytoplasm, distorted sinusoids, infiltration of mononuclear cells and necrotic zones. However, the severity of hepatic damage in IDPN-treated rats was independent of the magnitude of vestibular hair cell degeneration as well as the severity of behavioral deficits. Administration of IDPN in the vestibulotoxic doses did not produce any histological changes in the brain cortex and kidneys of rats.
亚氨基二丙腈(IDPN)是一种典型的腈类化合物,可在啮齿动物中引发兴奋、舞蹈症和转圈(ECC)综合征。先前的研究表明,前庭毛细胞变性与IDPN诱导的行为异常有关。尽管IDPN处理的大鼠前庭迷路的病理变化已有充分记录,但IDPN对其他器官系统的影响尚不清楚。因此,我们研究了暴露于IDPN的大鼠内耳、脑、肝和肾的组织病理学改变。成年雄性Wistar大鼠分为两组,每组六只动物。对照大鼠接受生理盐水,而IDPN组每天腹腔注射IDPN(100mg/kg),持续7天。仔细观察所有动物的任何行为异常,并对包括垂直和水平头部摆动、转圈和向后行走在内的运动障碍进行量化。在第9天处死动物,收集耳蜗、脑、肝和肾的样本进行组织病理学检查。结果显示,IDPN处理的大鼠行为缺陷的严重程度与壶腹嵴中的细胞损伤之间存在直接相关性。IDPN处理严重影响肝脏组织病理学,导致细胞质空泡化、肝血窦扭曲、单核细胞浸润和坏死区。然而,IDPN处理的大鼠肝脏损伤的严重程度与前庭毛细胞变性的程度以及行为缺陷的严重程度无关。给予前庭毒性剂量的IDPN不会在大鼠的大脑皮层和肾脏中产生任何组织学变化。