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1,25-二羟基维生素D_3对大鼠体重、血生化及CD4^+CD25^+Treg细胞的影响 被引量:1

Effects of 1,25-(OH)_2D_3 on body weight,blood biochemistry and regulatory CD4^+ CD25^+ Treg cells of experimental rats
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摘要 目的了解1,25-二羟基维生素D_3[1,25-(OH)_2D_3]对大鼠体重、血生化及CD4^+CD25^+Treg细胞的影响。方法 40只Lewis大鼠在正常膳食标准钙含量的状态下,分为对照组和1,25-(OH)_2D_30.125μg、0.25μg、1μg 3个剂量组,每周一、三、五分别灌胃给予相应剂量1,25-(OH)_2D_3,给药2 wk,对照组给予等容积赋形剂,每周3次记录大鼠体重变化,d 15在麻醉状态下留取大鼠外周血和脾脏组织,采用全自动生化分析仪检测血生化,流武细胞仪检测CD4^+CD25^+Treg细胞数量,real-time PCR法检测脾脏Foxp3 mRNA表达水平。结果与对照组相比,1,25-(OH)_2D_31μg组大鼠体重增长减慢(P<0.05);1μg组和0.25μg组大鼠血钙升高,0.125μg组大鼠血钙正常;1,25-(OH)_2D_3各剂量组大鼠血脂水平均轻度降低(P<0.05),外周血及脾脏CD4^+CD25^+Treg细胞的数量和脾脏Foxp3 mRNA表达水平显著升高(P<0.05),但肝、肾功能无显著影响(P>0.05)。结论在正常膳食的情况下,间断给予1,25-(OH)_2D_30.125μg大鼠血钙正常、对CD4^+CD25^+Treg细胞的诱导作用明显,安全有效。 AIM To investigate the effect of 1, 25-(OH) 2D3 on weight, blood biochemistry and CD4+ CD25 +Treg cells in rats. METHODS Fourty male Lewis rats fed standard chow divided into 4 groups and treated with either 0.125 μg, 0.25 μg, 1 μg of 1, 25- (OH) 2D3 or vehicle on Monday, Wednesday and Friday respectively for 2 weeks. Body weight of these rats was recorded 3 times a week. On day 15, the rats were anesthetized by amiodarone, peripheral blood and spleen tissues were taken to count CD4+ CD25+ Treg cells by flow cytometry. Expression of Foxp3 mRNA in spleen was measured by real- time PCR method. The blood calcium, lipids, liver function and renal function were examined by automatic biochemistry analyzer. RESULTS Compared with the control group, the increasing of rat body weight were delayed in the 1 μg dose of 1, 25- (OH) 2D3 group (P 〈 0.05). In addition, serum calcium of rats were increased in the 1 μg and 0.25 μg dose of 1, 25-(OH) 2D3 group (P 〈 0.05), but not in 0.125 μg group (P 〉 0.05) . The levels of blood lipids were decreased, the number of CD4+ CD25+ Treg cells in peripheral blood and spleen were increase and the mRNA expression of Foxp3 in spleen were enhanced in all 1, 25-(OH) 2D3 groups (P 〈 0.05). Moreover, liver and renal functions were no influences (P 〉 0.05) . CONCLUSION 1, 25- (OH) 2D3 with 0.125 μg interval treatment would be safe and effective with normal serum calcium and significant effects on CD4+ CD25+ Treg cells for rats fed standard chow.
出处 《中国新药与临床杂志》 CAS CSCD 北大核心 2012年第10期594-597,共4页 Chinese Journal of New Drugs and Clinical Remedies
基金 国家重点基础研究发展规划项目资助(2009CB522405)
关键词 1 25-二羟基维生素D_3 体重 自身免疫疾病 CD4^+ CD25^+ Treg细胞 Foxp3 1,25- (OH) 2D3 body weight calcium autoimmune diseases CD4+ CD25+Treg cells Foxp3
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  • 1BORGES MD, MARTINI LA, ROGERO MM, et 01. Current perspectives on vitamin D, immune system, and chronic disease [J]. Nutrition, 2011, 27(6): 399-404.
  • 2GUILLOT X, SEMERAO L, SAIDENBERG-KERMANAC HN, et al. Vitamin D and inflammation[J]. Joint Bone Spine, 2010, 77 (6): 552-557.
  • 3CANTORNA MT, HAYES CE, DeLUCA HF. 1, 25-Dihydroxy- cholecalciferol inhibits the progression of arthritis in murine modoels of human arthritis[J]. J Nutr, 1998, 128(1): 68-72.
  • 4CANTORNA MT, ZHU Y, FROICU M, et ol. Vitamin D status, 1,25-dihydroxyvitaminD3, and the immune system [J]. Am J Clin Nutr, 2004, 80 Suppl 1: 1717s-1720s.
  • 5ASCHEABRERNNER JK, SOLLINGER HW, BECKER BN, et 01. 1,25-(OH) 2D3 alters the transforming growth factor signaling pathway in renal[J]. J Surg Res, 2001, 100(2) : 171-175.
  • 6祁晓平,李培,恽时峰,黎介寿.1,25-二羟基维生素D3对致死剂量脂多糖攻击的大鼠CD_4^+CD_(25)^+Treg细胞的调节作用[J].中国现代普通外科进展,2011,14(9):676-679. 被引量:3
  • 7FONTENOT JD, GAVIN MA, RUDENSKY AY. Foxp3 programs the development and function of CD4 CD25 regulatory T cells [J]. Nat Immunol, 2003, 4(4): 330-336. A: 106-113.
  • 8DORINI L, PENNA G. Dendritic cell tolerogenicity: a key mechanism in immunomodulation by vitamin D receptor agonists [J]. Hum Immunol, 2009, 70(5) : 345-352.
  • 9dERLO A, TAGLIABUE E, MENARD S, et al. Matured human monoeyte-derive dendritic cells (MoDCs) induce expansion of CD4 CD25 Foxp3 T cells lacking regulatory properties[J]. Immunol Lett, 2008, 117 ( 1 ).

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  • 1陈晓颖,许红霞,李玲,赵燚,武震,张毓洪.维生素D受体基因多态性与脂代谢异常的相关研究[J].宁夏医科大学学报,2013,35(8):845-849. 被引量:2
  • 2李慧敏,缪珩,鲁一兵,成金罗,耿厚法,蒋秀琴.中国汉族人群维生素D受体基因多态性与糖尿病肾病的易感性[J].中国临床康复,2005,9(47):1-4. 被引量:15
  • 3Fernandez E,Fibla J,Betriu A,et al.Association between vitamin D receptor gene polymorphism and relative hypoparathyroidism in patients with chronic renal failure[J].J Am Soc Nephrol,1997,8(10):1546-1552.
  • 4VedralováM,Kotrbova-Kozak A,ZelezníkováV,et al.Polymorphisms in the vitamin D receptor gene and parathyroid hormone gene in the development and progression of diabetes mellitus and its chronic complications,diabetic nephropathy and non-diabetic renal disease[J].Kidney Blood Press Res,2012,36(1):1-9.
  • 5Lee S,Lee DK,Choi E,et al.Identification of a functional vitamin D response element in the murine Insig-2 promoter and its potential role in the differentiation of 3T3-L1 preadipocytes[J].Mol Endocrinol,2005,19(2):399-408.
  • 6Emerah AA,El-Shal AS.Role of vitamin D receptor gene polymorphisms and serum 25-hydroxyvitamin D level in Egyptian female patients with systemic lupus erythematosus[J].Mol Biol Rep,2013,40(11):6151-6162.
  • 7Mancuso P,Rahman A,Hershey SD,et al.1,25-DihydroxyvitaminD3 treatment reduces cardiac hypertrophy and left ventricular diameter in spontaneously hypertensive heart failure-prone(cp/+)rats independent of changes in serum leptin[J].J Cardiovasc Pharmacol,2008,51(6):559-564.
  • 8Jono S,Nishizawa Y,Shioi A,et al.1,25-Dihydroxyvitamin D3increases in vitro vascular calcification by modulating secretion of endogenous parathyroid hormone-related peptide[J].Circulation,1998,98(13):1302-1306.
  • 9Ortlepp JR,Hoffmann R,Ohme F,et al.The vitamin D receptor genotype predisposes to the development of calcific aortic valve stenosis[J].Heart,2001,85(6):635-638.
  • 10王笑云,孙彬,周富华,胡建明,俞香宝,彭韬.Vitamin D receptor and PCNA expression in severe parathyroid hyperplasia of uremic patients[J].Chinese Medical Journal,2001(4):74-78. 被引量:4

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