B. A. L. Dutra, C. Carneiro, Nayanna de Oliveira Ramos Melo, Gilson Brito de Oliveira, F. V. F. Jamacaru, João Crispim Ribeiro, C. A. Dornelas
{"title":"阿拉伯胶和丁香酚在硅诱导的Wistar大鼠炎症血管生成模型中的作用","authors":"B. A. L. Dutra, C. Carneiro, Nayanna de Oliveira Ramos Melo, Gilson Brito de Oliveira, F. V. F. Jamacaru, João Crispim Ribeiro, C. A. Dornelas","doi":"10.29169/1927-5951.2022.12.02","DOIUrl":null,"url":null,"abstract":"This work aims to evaluate the effects of gum arabic and eugenol on inflammatory angiogenesis in a subcutaneous silica inoculum model. Ninety-six Wistar rats were distributed over 16 groups. The substances administered by gavage included distilled water, gum arabic (500 mg/100g weight), and eugenol (10mg/100g weight). Control groups received 0.2 mL of sterile distilled water subcutaneously. The experimental groups were subjected to an inoculum of 0.2 mL of silica solution (50 mg/mL) subcutaneously. For seven or 14 days, the groups received distilled water or gum arabic or eugenol or gum arabic plus eugenol. There was no difference between the histological analysis of slides stained with hematoxylin-eosin. There was a reduction in vascular density in animals that received only gum arabic for 7 (0.09 µm² ± 0.02) or 14 (0.08 µm² ± 0.03) days and only eugenol for seven days (0.08 µm² ± 0.03), but this was not statistically significant. The microvascular density significantly increased in the group treated with eugenol for 14 days (0.14 µm² ± 0.02). Eugenol reduced inflammatory angiogenesis when administered for seven days and stimulated it when administered for 14 days. Gum arabic had a potential inhibitory effect on this model. The study of inflammatory angiogenesis, induced by a silica inoculum in the subcutaneous tissue of rats, is a new and reproducible model for evaluating angiogenesis and inflammation.","PeriodicalId":16959,"journal":{"name":"Journal of Pharmacy and Nutrition Sciences","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gum Arabic and Eugenol in a Silica-Induced Inflammatory Angiogenesis Model in Wistar Rat\",\"authors\":\"B. A. L. Dutra, C. Carneiro, Nayanna de Oliveira Ramos Melo, Gilson Brito de Oliveira, F. V. F. Jamacaru, João Crispim Ribeiro, C. A. Dornelas\",\"doi\":\"10.29169/1927-5951.2022.12.02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This work aims to evaluate the effects of gum arabic and eugenol on inflammatory angiogenesis in a subcutaneous silica inoculum model. Ninety-six Wistar rats were distributed over 16 groups. The substances administered by gavage included distilled water, gum arabic (500 mg/100g weight), and eugenol (10mg/100g weight). Control groups received 0.2 mL of sterile distilled water subcutaneously. The experimental groups were subjected to an inoculum of 0.2 mL of silica solution (50 mg/mL) subcutaneously. For seven or 14 days, the groups received distilled water or gum arabic or eugenol or gum arabic plus eugenol. There was no difference between the histological analysis of slides stained with hematoxylin-eosin. There was a reduction in vascular density in animals that received only gum arabic for 7 (0.09 µm² ± 0.02) or 14 (0.08 µm² ± 0.03) days and only eugenol for seven days (0.08 µm² ± 0.03), but this was not statistically significant. The microvascular density significantly increased in the group treated with eugenol for 14 days (0.14 µm² ± 0.02). Eugenol reduced inflammatory angiogenesis when administered for seven days and stimulated it when administered for 14 days. Gum arabic had a potential inhibitory effect on this model. The study of inflammatory angiogenesis, induced by a silica inoculum in the subcutaneous tissue of rats, is a new and reproducible model for evaluating angiogenesis and inflammation.\",\"PeriodicalId\":16959,\"journal\":{\"name\":\"Journal of Pharmacy and Nutrition Sciences\",\"volume\":\"38 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-04-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pharmacy and Nutrition Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.29169/1927-5951.2022.12.02\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacy and Nutrition Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29169/1927-5951.2022.12.02","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
摘要
本研究旨在评估阿拉伯树胶和丁香酚对皮下硅胶接种模型炎症血管生成的影响。96只Wistar大鼠分为16组。灌胃给药的物质包括蒸馏水、阿拉伯胶(500 mg/100g重量)和丁香酚(10mg/100g重量)。对照组皮下注射无菌蒸馏水0.2 mL。实验组小鼠皮下接种二氧化硅溶液0.2 mL (50 mg/mL)。连续7天或14天,各组分别饮用蒸馏水、阿拉伯胶或丁香酚或阿拉伯胶加丁香酚。苏木精-伊红染色载玻片的组织学分析无差异。只服用阿拉伯胶7天(0.09µm²±0.02)或14天(0.08µm²±0.03)和只服用丁香酚7天(0.08µm²±0.03)的动物血管密度降低,但无统计学意义。丁香酚处理14 d组微血管密度显著增加(0.14µm²±0.02)。丁香酚在给药7天后减少炎症血管生成,在给药14天后刺激炎症血管生成。阿拉伯胶对该模型有潜在的抑制作用。大鼠皮下注射二氧化硅诱导炎症性血管生成的研究,是评价血管生成和炎症的一种新的、可重复的模型。
Gum Arabic and Eugenol in a Silica-Induced Inflammatory Angiogenesis Model in Wistar Rat
This work aims to evaluate the effects of gum arabic and eugenol on inflammatory angiogenesis in a subcutaneous silica inoculum model. Ninety-six Wistar rats were distributed over 16 groups. The substances administered by gavage included distilled water, gum arabic (500 mg/100g weight), and eugenol (10mg/100g weight). Control groups received 0.2 mL of sterile distilled water subcutaneously. The experimental groups were subjected to an inoculum of 0.2 mL of silica solution (50 mg/mL) subcutaneously. For seven or 14 days, the groups received distilled water or gum arabic or eugenol or gum arabic plus eugenol. There was no difference between the histological analysis of slides stained with hematoxylin-eosin. There was a reduction in vascular density in animals that received only gum arabic for 7 (0.09 µm² ± 0.02) or 14 (0.08 µm² ± 0.03) days and only eugenol for seven days (0.08 µm² ± 0.03), but this was not statistically significant. The microvascular density significantly increased in the group treated with eugenol for 14 days (0.14 µm² ± 0.02). Eugenol reduced inflammatory angiogenesis when administered for seven days and stimulated it when administered for 14 days. Gum arabic had a potential inhibitory effect on this model. The study of inflammatory angiogenesis, induced by a silica inoculum in the subcutaneous tissue of rats, is a new and reproducible model for evaluating angiogenesis and inflammation.