Effects of bee products on pentylenetetrazole-induced seizures in the rat.

N Zárraga-Galindo, P Vergara-Aragón, S Rosales-Meléndez, P Ibarra-Guerrero, L E Domínguez-Marrufo, R E Oviedo-García, H Hernández-Ramírez, B Hernández-Téllez, I E López-Martínez, I Sánchez-Cervantes, M Vázquez-García, J Santiago
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Abstract

Bee products (BP) have been used for centuries as a diet complement with claimed curative properties. The aim of this study was to determine whether oral administration of BP prevented behavioral, histological, and biochemical alterations, caused by pentylenetetrazole (PTZ)-induced kindling in rats. Male Wistar rats were employed to evaluate seizure latency, number and duration, performance in the open field test, histological alterations and mortality following BP administration. Oral administration of BP at two doses, 30 and 60 mg/kg/day, significantly lengthened latency of both clonic and tonic PTZ-induced seizures, decreased the duration and frequency of seizures and reduced mortality. In the Open Field test, BP treated groups showed increases in the number of crossed squares and rearing counts, and on optimal dose, decreases in fecal boli. Histological analysis showed in PTZ (50 and 80 mg/kg) kindling rats, lungs with inflammatory peribronchiolar, and perialveolar infiltrates. In the liver, mild losses of trabeculae, multi-vesiculated hepatocytes (steatosis) and inflammatory infiltrates in hepatic parenchyma were observed. Interestingly, in the heart, fibers were markedly separated. In testis, stratified epithelium of seminal tubules lost its normal structure, tubules had epithelium loss, spermatids were absent, and spermatogonia and Leydig cells diminished. In PTZ kindling rats treated with BP, the lungs had no inflammatory infiltrates, although the heart showed some inflammatory infiltrates. Remaining structures had normal characteristics. These results, suggest that BP can protect rats from effects of PTZ-induced kindling.

蜂产品对戊四唑致大鼠癫痫发作的影响。
几个世纪以来,蜂产品(BP)一直被用作一种饮食补充,声称具有疗效。本研究的目的是确定口服BP是否能预防戊四唑(PTZ)诱导的大鼠点火引起的行为、组织学和生化改变。采用雄性Wistar大鼠评估癫痫发作潜伏期、次数和持续时间、野外试验表现、BP给药后的组织学改变和死亡率。口服BP两种剂量(30和60 mg/kg/天)可显著延长ptz引起的阵挛性和强直性癫痫发作的潜伏期,减少癫痫发作的持续时间和频率,降低死亡率。在Open Field试验中,BP处理组的交叉方格数和饲养计数增加,在最佳剂量下,粪粪数量减少。组织学分析显示PTZ(50和80 mg/kg)点燃大鼠,肺部有炎性细支气管周围浸润和肺泡周围浸润。在肝脏中,观察到轻度小梁丢失,肝细胞多囊化(脂肪变性)和肝实质炎症浸润。有趣的是,在心脏中,纤维明显分离。在睾丸中,精管层状上皮失去正常结构,精管上皮丢失,精子缺失,精原细胞和间质细胞减少。BP治疗后PTZ点火大鼠肺无炎性浸润,心脏有部分炎性浸润。其余结构特征正常。这些结果表明,BP可以保护大鼠免受ptz诱导的点火效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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