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Oral treatment with a rattlesnake native polypeptide crotamine efficiently inhibits the tumor growth with no potential toxicity for the host animal and with suggestive positive effects on animal metabolic profile

机译:用响尾蛇的原生多肽克拉唑胺的口腔治疗有效地抑制肿瘤生长,对宿主动物没有潜在的毒性,并对动物代谢概况提出暗示性积极影响

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The efficacy of crotamine as antitumoral was first demonstrated by daily intraperitoneal (IP) injections of low doses of this toxin in an animal model bearing melanoma tumors. Significant inhibition of tumor growth and increased lifespan of mice bearing tumor was also noticed after 21 consecutive days of this daily IP administration of crotamine. However, due to the limited acceptance of treatments by IP route in clinical conditions, herein, we evaluated the antitumor effect of this native polypeptide employing the oral route. The efficacy of crotamine in inhibiting the melanoma growth in vivo, even after passing through the gastrointestinal tract of the animal, was confirmed here. In addition, biochemical biomarkers and also histopathological analysis showed both the absence of any potential toxic effects in tissues or organs of the animal in which the highest accumulation of crotamine is expected. Interestingly, a reduction of weight gain was observed mainly in animals with tumor treated with crotamine by IP route, but not by oral administration. Albeit, oral administered crotamine was able to significantly decrease the body weight gain of healthy animals without tumor. Taking advantage of this same experimental animal models receiving crotamine by oral route, it was possible to show metabolic changes as the increased capacity of glucose clearance, which was accompanied by a reduction of the total cholesterol, and by increased high-density lipoprotein levels, both observed mainly in the absence of tumor. Triglycerides and low-density lipoprotein were also significantly decreased, but only in the absence of tumor. Taken together, these data suggest a clear trend for metabolic positive effects and mischaracterize unhealthy condition of animals, with or without tumors, treated with crotamine for 21 days. In addition, this study confirmed the efficacy of crotamine administered by oral route as antitumor agent, which besides the additional advantage of administration convenience and decreased risk of toxic effects, allowed the serendipitous observation of several positive metabolic effects on treated animals.
机译:首先通过在患有黑色素瘤肿瘤的动物模型中的每日腹膜内(IP)注射低剂量这种毒素的腹膜内(IP)注射抗肿瘤的疗效。在每日IP施用克拉唑胺的每日IP施用后21天后,还注意到患有肿瘤患者肿瘤的肿瘤生长和增加的小鼠寿命的显着抑制。然而,由于在临床条件下的IP路线接受治疗的接受有限,在此,我们评估了使用口腔途径的该天然多肽的抗肿瘤效应。这里证实了克罗那在体内抑制体内黑色素瘤生长的疗效,即使在通过动物的胃肠道之后。此外,生物化学生物标志物以及组织病理学分析表明,预期克拉妥的最高积累的动物组织或器官中没有任何潜在的毒性作用。有趣的是,在通过IP途径用克拉胺处理的肿瘤处理的动物中,观察到体重增加的减少,但不是口服给药。虽然,口服施用的克拉胺能够显着降低健康动物的体重增加而没有肿瘤。利用口服途径接受克拉胺的相同实验动物模型,可以表现出代谢变化作为葡萄糖间隙的增加,这伴随着总胆固醇的减少,并且通过增加的高密度脂蛋白水平主要在没有肿瘤的情况下观察到。甘油三酯和低密度脂蛋白也显着降低,但仅在没有肿瘤的情况下。总之,这些数据表明了一种明显的代谢阳性效应趋势,并在没有肿瘤的情况下用或没有肿瘤的药物不健康状况,用克罗莎治疗21天。此外,本研究证实了口服途径给予抗肿瘤剂的克拉胺的疗效,除了给予方便的额外优势和毒性作用的风险降低,允许对治疗动物进行几种阳性代谢作用的偶然观察。

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