您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(医学版)》

山东大学学报(医学版) ›› 2014, Vol. 52 ›› Issue (9): 48-53.doi: 10.6040/j.issn.1671-7554.0.2014.033

• 基础医学 • 上一篇    下一篇

Ghrelin对兔激素性股骨头缺血性坏死中VEGF的影响

黄来刚, 崔宝娟, 王晓红, 王道清, 曾凡硕, 孙敏, 刘本玲, 孙强三   

  1. 山东大学第二医院康复医学科, 山东 济南 250033
  • 收稿日期:2014-01-14 修回日期:2014-09-04 出版日期:2014-09-10 发布日期:2014-09-10
  • 基金资助:
    山东省自然科学基金(ZR2009CM123)

Effect of Ghrelin on the VEGF expression in steroid-induced avascular necrosis of the femoral head in rabbits

HUANG Laigang, CUI Baojuan, WANG Xiaohong, WANG Daoqing, ZENG Fanshuo, SUN Min, LIU Benling, SUN Qiangsan   

  1. Department of Rehabilitation, Second Hospital of Shandong University, Jinan 250033, Shandong, China
  • Received:2014-01-14 Revised:2014-09-04 Online:2014-09-10 Published:2014-09-10
  • Contact: 孙强三。E-mail:sunqsan@126.com E-mail:sunqsan@126.com

摘要: 目的 观察Ghrelin对兔激素性股骨头缺血性坏死(sANFH)中血管内皮生长因子(VEGF)表达的影响。方法 选择24周龄以上雄性新西兰兔34只,随机分为正常组(n=8)和造模组(n=26)。造模采用马血清联合甲基强的松龙的方法,每组各取4只行股骨头磁共振及病理组织学检查,明确造模是否成功。将造模组造模成功的20只随机分为对照组(n=10)和Ghrelin干预组(n=10),正常组剩余4只纳入空白组。Ghrelin干预组连续2周耳缘静脉注射Ghrelin[25μg/(kg·d)],对照组连续2周耳缘静脉注射相同剂量生理盐水;2周后空气栓塞法处死动物,收集标本,行股骨头组织形态学观察、RT-PCR法检测股骨头组织中VEGF的表达。结果 对照组股骨头病理组织学检查可见骨小梁广泛稀疏、大部分断裂,脂肪细胞可见融合现象;Ghrelin干预组可见骨小梁稀疏,偶见断裂;脂肪细胞较多并轻度肥大,在骨髓中所占比例多于正常组,未见融合现象。RT-PCR法检测结果显示,对照组和Ghrelin干预组VEGF表达均高于空白组(P<0.05);同时Ghrelin干预组VEGF表达明显高于对照组(P<0.05)。结论 Ghrelin可促进激素性缺血性股骨头坏死组织中VEGF mRNA的表达,从而改善坏死股骨头组织微循环,进一步改善激素性缺血性股骨头坏死的进程。

关键词: 激素性缺血性股骨头坏死, 血管内皮生长因子, 兔, 磁共振, Ghrelin

Abstract: Objective To observe the effect of Ghrelin on the expression of vascular endothelial growth factor (VEGF) in steroid-induced avasular necrosis of the femoral head in rabbits. Methods A total of 34 male New-Zealand rabbits which aged more than 24 weeks were divided into normal group (n=8) and model group (n=26). Models of steroid-induced avascular necrosis of femoral head were induced by horse serum combined with hormone methylprednisolone. After that, 4 rabbits were selected from each group randomly to determine with MRI and histopathological examinations if the modeling was successful. The 20 successfully modeled rabbits were divided into control group (n=10) and Ghrelin intervention group (n=10), and the remaining 4 in the normal group were classified as blank group. Rabbits in Ghrelin intervention group received Ghrelin injection (25 μg/kg·d) for 2 weeks, and rabbits in control group were given the same dose of saline for 2 weeks. Samples were collected after the animals were sacrificed. The histomorphology of femoral head was examined, and VEGF mRNA level was detected with Real-time PCR. Results The control group displayed extensive sparse and broken trabecula, and adipocytes were fused. The Ghrelin intervention group showed occasionally broken sparse trabecula. The adipocytes were slightly hypertrophic but not fused, with a higher proportion in the marrow than in the control group. VEGF mRNA expression was higher in Ghrelin intervention group and controlgroup than in blank group (P<0.05), and it was higher in the Ghrelin intervention group than in the control group (P<0.05). Conclusion Ghrelin can up-regulate the expression of VEGF in steroid-induced avasular necrosis of femoral head in rabbits, and improve the microcirculation and progression of femoral head.

Key words: Avascular necrosis of the femoral head, Ghrelin, Rabbits, Vascular Endothelial Growth Factor, Magnetic Resonance Imaging

中图分类号: 

  • R493
[1] 尤全喜.专家谈股骨头坏死[M]. 北京:中医古籍出版社,2003:10-12.
[2] Cummings D E, Shannon M H.Roles for ghrelin in the regulation of appetite and body weight[J]. Arch Surg, 2003, 138(4):389-396.
[3] Horvath, Diano S, Sotonyi P, et al. Minireview:ghrelin and the regulation of energy balance-a hypothalamic per-spective[J]. Endocrinology, 2001,142(10):4163-4169.
[4] Kojima M, Hosoda H, Date Y, et al. Ghrelin is a growth-hormone-releasing acylated peptide from stomach[J]. Nature, 1999, 402(6762):656-660.
[5] Date Y, Kojima M, Hosoda H, et al.Ghrelin, a novel growth hormone-releasing acylated peptide, is synthesized in a distinct endocrine cell type in the gastrointestinal tracts of rats and humans[J]. Endocrinology, 2000, 141(11):4255-4261.
[6] Gualillo O, Caminos J E, Kojima M, et al. Gender and gonadal influences on ghrelin mRNA levels in rat stomach[J]. Eur J Endocrinol, 2001, 144(6):687-690.
[7] Bowers C Y. Unnatural growth hormone-releasing peptide begets natural ghrelin[J]. J Clin Endocrinol Metab, 2001, 86(4):1464-1469.
[8] Date Y, Murakami N, Kojima M,et al.Central effects of a novel acylated peptide, ghrelin, on growth hormone release in rats[J]. Biochem Biophys Res Commun, 2000, 275(2):477-480.
[9] Sakata I, Nakamura K, Yamazaki M, et al. Ghrelin-producing cells exist as two types of cells, closed- and opened-type cells, in the rat gastrointestinal tract[J]. Peptides, 2002, 23(3):531-536.
[10] Delhanty P J, van der Eerden B C, van Leeuwen J P.Ghrelin and bone[J]. Biofactors, 2014, 40(1):41-48.
[11] Liang Q H, Liu Y, Wu S S, et al. Ghrelin inhibits the apoptosis of MC3T3-E1 cells through ERK and AKT signaling pathway [J]. Toxicol Appl Pharmacol, 2013, 272(3):591-597.
[12] Fukushima N, Hanada R, Teranishi H, et al. Ghrelin directly regulates bone formation [J]. J Bone Miner Res, 2005, 20(5):790-798.
[13] Maccarinelli G, Sibilia V, Torsello A, et al. Ghrelin regulates proliferation and differentiationof osteoblastic cells[J]. J Endocrinol, 2005, 184(1):249-256.
[14] Fukushima N, Hanada R, Teranishi H, et al. Ghrelin directly regulates bone formation[J]. J Bone Miner Res, 2005, 20(5):790-798.
[15] Maccarinelli G, Sibilia V, Torsello A,et al.Ghrelin reg-ulates proliferation and differentiation of osteoblastic cells [J]. J Endocrinol, 2005, 184(1):249-256.
[16] Larsson B, Norlén P, Lindström E, et al. Effects of ECL cell extracts and granule/vesicle-enriched fractions from rat oxyntic mucosa on cAMP and IP(3) in rat osteoblast-like cells[J]. Regul Pept, 2002, 106(1-3):13-18.
[17] Kerachian M A, Harvey E J, Cournoyer D, et al. Avascular necrosis of the femoral head: vascular hypotheses [J]. Endothelium, 2006, 13(4):237-244.
[18] Feng L, Wu H, E L, et al.Effects of vascular endothelial growth factor 165 on bone tissue engineering [J]. PLoS ONE, 2013, 8(12):82945.
[19] Turner N, Grose R. Fibroblast growth factor signalling:from development to cancer [J]. Nat Rev Cancer, 2010, 10(2):116-129.
[20] Horner A, Bishop N J, Bord S, et al. Immunolocalisation of vascular endothelial growth factor (VEGF) in human neonatal growth plate cartilage[J]. J Anat, 1999, 194(4):519-524.
[21] Petersen W, Pufe T, Zantop T, et al. Expression of VEGFR-1 and VEGFR-2 in degenerative Achilles tendons [J]. Jorthop Res, 2004(420):286-291.
[22] Pufe T, Claassen H, Scholz-Ahrens K E, et al. Influence of estradiol on vascular endothelial growth factor expression in bone: a study in Göttingen miniature pigs and human osteoblasts [J]. Calcif Tissue Int, 2007, 80(3):184-191.
[23] Vadasz Z, Misselevich I, Normman D, et al. Localization of vascular endothelial growth factor during the early reparative phase of the rats' vessels deprivation-induced osteonecrosis of the femoral heads [J]. Exp Mol Pathol, 2004, 77(2):145-148.
[1] 王韶卿 刘毅慧 付婷婷 成金勇 刘强. 肝癌31磷磁共振波谱数据的分类[J]. 山东大学学报(医学版), 2209, 47(6): 42-46.
[2] 黄方 康瑞 吴春林. VEGFC、NF-κBp65及Survivin在鼻咽癌中的表达及临床意义[J]. 山东大学学报(医学版), 2209, 47(6): 83-.
[3] 金晨曦,沈薇,李娜,孙建锋,杨驰,郭泾. ADDWoR关节镜下盘复位术盘-髁运动的定量分析[J]. 山东大学学报 (医学版), 2025, 63(7): 54-61.
[4] 王磊,常霄,王梓萌,李娇娇,崔书君,杨飞,朱月香. 瘤内及瘤周DCE-MRI影像组学对宫颈癌患者无进展生存期的预测价值[J]. 山东大学学报 (医学版), 2025, 63(6): 45-54.
[5] 单体晓,杜韦辰,王勤周,李安宁,李春海. 自身免疫性郎飞结病磁共振成像研究进展[J]. 山东大学学报 (医学版), 2025, 63(11): 117-122.
[6] 刘晶晶,庞婧,赵晓丹,林昕,付敏,陈静静. 基于乳腺X线摄影及DCE-MRI机器学习模型预测乳腺癌新辅助治疗后病理完全缓解:双中心研究[J]. 山东大学学报 (医学版), 2025, 63(1): 60-72.
[7] 姜俊,高洪莲,孙瑞婷,孙昕,彭庆生,张守宽,张磊. 血管内皮生长因子-B对形觉剥夺性近视豚鼠视网膜中多巴胺水平的影响[J]. 山东大学学报 (医学版), 2024, 62(7): 62-71.
[8] 刘小文,曹永泉,侯明源,于德新. EOB-MRI多定量参数对肝胆期乏血供低信号结节进展风险的评估价值[J]. 山东大学学报 (医学版), 2024, 62(4): 31-39.
[9] 吴思雨,沈业隆,王锡明. 影像组学预测原发性中枢神经系统淋巴瘤的Ki-67标记指数[J]. 山东大学学报 (医学版), 2024, 62(11): 67-72.
[10] 靳新娟,左立平,邓展昊,李安宁,于德新. MRI影像组学对135例肝癌耐药蛋白PFKFB3的预测价值[J]. 山东大学学报 (医学版), 2023, 61(6): 79-86.
[11] 李晴,张安娜,杜艳圣,刁久洲,崔若瑾,付鹏蕊,岳欣毅,周庆博. 47例单个脊髓炎性脱髓鞘病灶转化的影响因素[J]. 山东大学学报 (医学版), 2023, 61(5): 37-43.
[12] 王磊,张帅,刘钢,由胜男,王植,朱珊,陈超,马信龙,杨强. MRI诊断140例腰椎智能网络自动检测分型MCs方法的比较[J]. 山东大学学报 (医学版), 2023, 61(3): 71-79.
[13] 杨咏青,赵鹏,汪玉,马文静,田迷迷,程亚旎,祖璐,林祥涛. 细胞外容积分数对62例不同病理类型肺癌的诊断价值[J]. 山东大学学报 (医学版), 2023, 61(2): 88-94.
[14] 靳新娟,蔡大幸,范金蕾,邓展昊,李楠,于德新,李安宁. 显微镜高分辨率MRI鉴别皮肤良、恶性局灶隆起性结节[J]. 山东大学学报 (医学版), 2023, 61(12): 51-61.
[15] 赵恩举,赵硕,郭云亮,王锡明. 282例颈动脉钙化与脑小血管病MRI总负荷评分的关联性[J]. 山东大学学报 (医学版), 2023, 61(1): 38-44.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!