{"title":"Antimitotic effects of Cysticercus tenuicollis protoscolexes extract at administration to mice and their negative consequences for organism","authors":"","doi":"10.31016/1998-8435-2023-17-1-124-133","DOIUrl":null,"url":null,"abstract":"The purpose of the research is studying of Cysticercus tenuicollis protoscolexes extract effects on cell division at different routes of administration to mice and evaluation of the associated negative effects.Materials and methods. C. tenuicollis were obtained from spontaneously infected sheep in Kabardino-Balkarian Republic. C. tenuicollis protoscolexes were washed, crushed and homogenized. Protein extraction was performed with phosphate buffered saline pH 7.2–7.4. C. tenuicollis extract was administered intraperitoneally and intravenously to mice males at the dose level of 80 μg protein/animal. The control group of mice was intravenously injected with 0.1 ml of saline. At hours 3; 6; 24 and 48 post extract administration mice were euthanized. Bone marrow samples were taken from experimental and control mice for preparation of microscopic preparations to assess mitotic activity in a given cell population. The mitotic index was determined, all stages of mitosis were recorded. At the above time points blood samples were taken from mice to determine the main hematological parameters post intravenous and intraperitoneal administration of C. tenuicollis extract. The main hematological parameters of mice were determined using hematological analyzer MicroCC-20 Plus (High Technology, Inc. (USA)); leukocyte formula – by the generally accepted method. Samples of liver, kidneys, spleen, mesenteric lymph nodes and testes were taken from experimental and control animals for macroscopic and microscopic studies.Results and discussion. C. tenuicollis protoscolices extract leads to inhibition of cell division in the population bone marrow and testes cells in mice when administered intravenously and intraperitoneally at the dose level of 80 μg/animal manifested in accumulation of metaphases and decrease of other stages. At both routes of administration a decrease in leukocyte counts was noted. The observed microscopic changes in testes, spleen and lymph nodes either reflect the consequences of extract antimitotic effect or the immune response to the administration of C. tenuicollis extract.","PeriodicalId":34353,"journal":{"name":"Rossiiskii parazitologicheskii zhurnal","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rossiiskii parazitologicheskii zhurnal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31016/1998-8435-2023-17-1-124-133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The purpose of the research is studying of Cysticercus tenuicollis protoscolexes extract effects on cell division at different routes of administration to mice and evaluation of the associated negative effects.Materials and methods. C. tenuicollis were obtained from spontaneously infected sheep in Kabardino-Balkarian Republic. C. tenuicollis protoscolexes were washed, crushed and homogenized. Protein extraction was performed with phosphate buffered saline pH 7.2–7.4. C. tenuicollis extract was administered intraperitoneally and intravenously to mice males at the dose level of 80 μg protein/animal. The control group of mice was intravenously injected with 0.1 ml of saline. At hours 3; 6; 24 and 48 post extract administration mice were euthanized. Bone marrow samples were taken from experimental and control mice for preparation of microscopic preparations to assess mitotic activity in a given cell population. The mitotic index was determined, all stages of mitosis were recorded. At the above time points blood samples were taken from mice to determine the main hematological parameters post intravenous and intraperitoneal administration of C. tenuicollis extract. The main hematological parameters of mice were determined using hematological analyzer MicroCC-20 Plus (High Technology, Inc. (USA)); leukocyte formula – by the generally accepted method. Samples of liver, kidneys, spleen, mesenteric lymph nodes and testes were taken from experimental and control animals for macroscopic and microscopic studies.Results and discussion. C. tenuicollis protoscolices extract leads to inhibition of cell division in the population bone marrow and testes cells in mice when administered intravenously and intraperitoneally at the dose level of 80 μg/animal manifested in accumulation of metaphases and decrease of other stages. At both routes of administration a decrease in leukocyte counts was noted. The observed microscopic changes in testes, spleen and lymph nodes either reflect the consequences of extract antimitotic effect or the immune response to the administration of C. tenuicollis extract.
本研究旨在研究不同给药途径的细囊尾蚴原头节提取物对小鼠细胞分裂的影响,并评价其相关的负面影响。材料和方法。从卡巴尔达-巴尔干共和国自发感染的绵羊中分离到细纹线虫。洗净,粉碎,均质化。用pH 7.2-7.4的磷酸盐缓冲盐水提取蛋白质。以80 μg蛋白/只的剂量水平,分别腹腔和静脉给药雄性小鼠。对照组小鼠静脉注射生理盐水0.1 ml。3小时;6;分别对24和48只给药后小鼠实施安乐死。骨髓样本取自实验小鼠和对照小鼠,用于制备显微镜制剂,以评估给定细胞群中的有丝分裂活性。测定有丝分裂指数,记录有丝分裂的各个阶段。在上述时间点取小鼠血样,测定静脉和腹腔给药后的主要血液学参数。小鼠主要血液学参数采用血液分析仪MicroCC-20 Plus (High Technology, Inc. (USA))测定;白细胞配方-采用普遍接受的方法。取实验动物和对照动物的肝脏、肾脏、脾脏、肠系膜淋巴结和睾丸标本进行宏观和微观研究。结果和讨论。以80 μg/只的剂量给药和腹腔给药时,细棘原脊柱提取物均能抑制小鼠群体骨髓和睾丸细胞的细胞分裂,表现为中期细胞的积累和其他阶段细胞的减少。两种给药方式均可观察到白细胞计数的减少。观察到的睾丸、脾脏和淋巴结的微观变化可能反映了提取物抗有丝分裂作用的后果,也可能反映了对细刺草提取物的免疫反应。