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载阿苯达唑和黄连素牛血清白蛋白纳米粒对实验旋毛虫病肠道期和肌幼虫期的治疗效果。

Therapeutic efficacy of albendazole and berberine loaded on bovine serum albumin nanoparticles on intestinal and muscular phases of experimental trichinellosis.

机构信息

Department of Parasitology, Theodor Bilharz Research Institute, Kornaish El-Nile St., 12411, Giza, Egypt.

Medical technology center, Medical Research Institute, Alexandria University, Egypt.

出版信息

Acta Trop. 2023 May;241:106896. doi: 10.1016/j.actatropica.2023.106896. Epub 2023 Mar 14.

Abstract

There has been no treatment for trichinellosis until now. Therefore, this work targeted to investigating the efficacy of albendazole and berberine alone and loaded on bovine serum albumin (BSA) nanoparticles against intestinal and muscular phases of trichinellosis in mice. Mice were divided into nine different groups: negative control, positive control, blank nanoparticle, albendazole, berberine, a combination of albendazole and berberine, albendazole-loaded nanoparticle, berberine-loaded nanoparticle and combination of albendazole and berberine-loaded nanoparticle. Subsequently, they were sacrificed 6 and 35 days after infection. Treatment efficacies were parasitologically, histopathologically and, immunohistochemically assessed. Parasitological counting for the adult worms and encysted larvae with histopathological assessment using H&E for intestinal and muscular sections and picrosirius red stain for muscular sections were used. Also, immunohistochemical expression of the intestinal nod-like receptor-pyrin domain containing 3 (NLRP3) was investigated. The group treated with nano_combined drugs showed a statistically significant reduction in adult and encysted larval count (p<0.005), a remarkable improvement of intestinal and muscular inflammation, and a reduction in the capsular thickness of the larvae. Also, this group showed the highest reduction of NLRP3 expression. This work revealed that berberine might be a promising anti-trichinellosis drug with a synergistic effect when combined with albendazole through modulation of the immune response, inflammation, and larva capsule formation. Furthermore, delivering both drugs in a nanoparticle form improves their therapeutic response.

摘要

到目前为止,还没有治疗旋毛虫病的方法。因此,这项工作的目的是研究阿苯达唑和黄连素单独以及负载在牛血清白蛋白(BSA)纳米粒子上对小鼠肠期和肌期旋毛虫病的疗效。将小鼠分为九个不同的组:阴性对照组、阳性对照组、空白纳米粒子组、阿苯达唑组、黄连素组、阿苯达唑和黄连素联合组、阿苯达唑负载纳米粒子组、黄连素负载纳米粒子组和阿苯达唑和黄连素联合负载纳米粒子组。然后,在感染后第 6 天和第 35 天处死它们。用寄生虫学、组织病理学和免疫组织化学方法评估治疗效果。用成年蠕虫和囊包幼虫的寄生虫计数,用 H&E 对肠和肌肉切片进行组织病理学评估,用皮尔斯红染色对肌肉切片进行评估。还研究了肠道结节样受体-吡喃域包含 3(NLRP3)的免疫组织化学表达。用纳米联合药物治疗的组在成年和囊包幼虫计数方面表现出统计学上的显著降低(p<0.005),肠和肌肉炎症显著改善,幼虫囊包厚度降低。此外,该组表现出 NLRP3 表达的最大降低。这项工作表明,黄连素可能是一种有前途的抗旋毛虫病药物,与阿苯达唑联合使用时通过调节免疫反应、炎症和幼虫囊包形成具有协同作用。此外,将两种药物以纳米粒子的形式给药可以提高它们的治疗反应。

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