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菟丝子醇提液对衰老模型大鼠脾淋巴细胞DNA损伤影响的研究 被引量:6

Effect of alcoholic extract of semen cuscutae on DNA damage in spleen lymphocytes of aging model rats
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摘要 目的:探讨菟丝子醇提液对衰老模型大鼠脾淋巴细胞DNA损伤的保护作用。方法:Wistar大鼠40只,按体重随机分为青年对照组(8只)、衰老模型组(8只)、菟丝子给药组(24只),菟丝子给药组又分为给药15d、30d和45d组。采用D-半乳糖法制作衰老模型,按0.8g/kg.d剂量经胃灌服菟丝子醇提液。采用单细胞凝胶电泳(SCGE)技术检测脾淋巴细胞DNA损伤程度,同时观察不同给药天数对其影响。结果:衰老模型大鼠脾淋巴细胞DNA拖尾率较青年组明显升高(P<0.01),不同菟丝子醇提液给药组均可降低大鼠脾淋巴细胞DNA拖尾率(P<0.01),以给药45d效果最显著(P<0.01)。结论:菟丝子醇提液对D-半乳糖衰老模型大鼠脾淋巴细胞DNA损伤具有保护作用,且呈现时间依赖性。 Objective: To study the protective action of alcoholic extract of semen cuscutae (AESC) upon DNA damage in in spleen lymphoeytes of aging model rats. Method:Forty Wistar rats were randomly divided into young(8) ,aging(8) ,and three different administration groups of 15d, 30 d and 45 d(24). Aging rat models were made by D--gal injection,the AESC was drenched by a transgastric approach at the dosage of 0. 8g/kg.d. We ssayed the DNA damage in spleen tymphocytes of aging model rat by the single cell gel electrophoresis (SCGE) technique; at the same time, the effects of different days with AESC were observed. Results:Compared with the control group, the percentage of cells with comets of spleen in aging model rat increased (P 〈 0. 05) ; drenched by the AESC the percentage of cells with comets of spleen in aging model rat decreased (P 〈 0.05). Conclusions:AESC can protect DNA damage of the spleen lymphocytes in aging rat induced by D -gal. And the protect Presents time dependence.
出处 《黑龙江医药科学》 2009年第3期2-2,3,共2页 Heilongjiang Medicine and Pharmacy
关键词 菟丝子醇提液 衰老模型大鼠 脾淋巴细胞 DNA损伤 alcoholic extract of semen cuscutae aging model rats spleen lymphocyte DNA damage
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  • 1段链,杨静玉,于海,吴春福.彗星试验中全血法与分离淋巴细胞法的比较[J].癌变·畸变·突变,2004,16(5):307-309. 被引量:21
  • 2乔琰,鲁志松,姚汉超,杨旭,李睿.彗星试验分析指标的进展和应用[J].卫生毒理学杂志,2004,18(3):190-192. 被引量:26
  • 3李学军.慢性铍病发生的免疫病理机制[J].职业卫生与病伤,1995,10(2):110-114. 被引量:4
  • 4Chin L, Artandi SE. Shen O, et al. p53 deficiency rescues the adverse effects of telomere loss and cooperates with telomere dysfunction to accelerate carcinogenesis. Cell 1999: 97:527 - 38.
  • 5Gonzalez-Suarez E, Samper E, Flores JM, et al. Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesis. Nat Genet 2000; 26:114- 7.
  • 6Morales CP, Holt SE, Ouellette M, et al. Absence of cancer-associated changes in human fihroblasts immortalized with telomerase.Nat Genet 1999; 21:115 -8.
  • 7Kiyono T. Foster SA, Koop JI, et al. Both Rb/p16INK4a inactivation and telomerase activity are required to immortalize human epithelial cells. Nature 1998;396:84 - 8.
  • 8Ramirez RD. Morales CP, Herbert BS,et al. Putative telomere-independent mechanisms of replicative aging reflect inadequate growth conditions. Genes De 2001;15:398 -403.
  • 9Stampfer MP, Garbe J, Levine G, et al. Expression of the telomeraes catalytic subunit, hTER, induces resistance to transforming grouwth factor-beta growth inhabition in pl6INK4A( - ) human mammary epithelial cells. Proc Natl Acad Sci USA 2001; 98:4498 -503.
  • 10Gonzalez-Suarez E, Samper E, Ramirez A, et czl. Increased epithelial tumors anf increased wound healing in transgenic mice overexpressing the catalytic subunit of telomerase, mTERT, in basal keratinocytes. EMBO J 2001; 20:2619 -30.

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