...
首页> 外文期刊>In vivo. >Application-dependent immunomodulating and antimetastatic efficacy of thymic peptides in BALB/c-mice.
【24h】

Application-dependent immunomodulating and antimetastatic efficacy of thymic peptides in BALB/c-mice.

机译:胸腺肽在BALB / c-小鼠中的应用依赖性免疫调节和抗转移功效。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The immunomodulating and antimetastatic activity of clinically approved, low molecular weight, standardized thymic peptide (TP) preparations was evaluated in BALB/c-mice. Daily applications (subcutaneously, s.c.; intraperitoneally, i.p.; intramusculary, i.m.) of two commercially available TP preparations (7 consecutive days, 10, 50 and 100 micrograms per mouse and injection) up-regulated the thymus weight and thymocyte counts as well as peripheral blood leukocyte and lymphocyte counts in liver metastases-bearing mice. The immunomodulating activity of TP application was most pronounced and statistically significant for thymus weight and counts of thymocytes, leukocytes and lymphocytes after s.c. administration of both TP preparations and concentrations. I.p. and i.m. TP-injections were less effective at reaching statistical significance, however, for defined dosages and parameters, only. To evaluate the influence of TP on experimental liver metastases, RAW 117 lymphosarcoma cells were intravenously inoculated into BALB/c-mice. TP (10, 50, 100 micrograms/mouse) were s.c., i.p. and i.m. administered daily for 7 consecutive days starting 24 hours after tumor cell challenge. Liver colonization was investigated on day 14 after tumor cell inoculation and demonstrated a statistically significant (p < 0.05) reduction of experimental liver metastases for s.c. (both preparations and concentrations) as well as i.p. and i.m. (dose-dependent) TP-treated mice.
机译:在BALB / c-小鼠中评估了临床认可的低分子量标准化胸腺肽(TP)制剂的免疫调节和抗转移活性。两种市售TP制剂(连续7天,每只小鼠和注射剂连续7天,10、50和100微克)的每日应用(皮下,皮下,腹膜内,腹膜内,ip,肌内注射)上调了胸腺重量和胸腺细胞计数以及外周血荷肝转移小鼠的血白细胞和淋巴细胞计数。 TP的免疫调节活性在s.c.之后对胸腺重量和胸腺细胞,白细胞和淋巴细胞的计数最为显着并且在统计学上显着。 TP制剂和浓度的管理。 I.p.和我TP注射仅在确定剂量和参数时才能达到统计学上的显着效果。为了评估TP对实验性肝转移的影响,将RAW 117淋巴肉瘤细胞静脉内接种到BALB / c-小鼠中。 TP(10、50、100微克/小鼠)s.c.,i.p.和我肿瘤细胞攻击后24小时开始,连续7天每天服用。在接种肿瘤细胞后的第14天研究了肝定植,结果显示,经皮囊性肝癌的实验性肝转移在统计学上有显着降低(p <0.05)。 (制剂和浓度)以及i.p.和我(剂量依赖性)TP处理的小鼠。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号