用户名: 密码: 验证码:
针刀松解法对膝骨关节炎大鼠中枢镇痛作用影响的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
骨关节炎(Osteoarthritis, OA)是全球范围内极为常见的一种骨关节病,具有较高的致残率,因对患者生活、家庭及社会产生重要的影响而备受医疗机构的关注。2000年的世界卫生组织大会宣布2000-2010年为防治骨关节炎的十年,2002年中国卫生部、中华医学会宣布2002-2012年为“中国骨骼与关节健康十年”。膝关节是骨关节炎的好发部位,膝骨关节炎(Knee Osteoarthritis, KOA)以膝关节疼痛、僵硬、活动受限为主要特征,患者常因关节疼痛而求治。
     针刀松解法在膝骨关节炎的治疗方面取得了较好的疗效,目前对针刀疗法的研究逐渐向基础研究领域深入发展,本课题依托国家重点基础研究发展计划(973计划)中医理论资助专项《针刀松解法基础研究》的研究,通过动物实验探讨针刀松解法镇痛的作用及其中枢机制,为验证针刀疗法的有效性提供客观依据。
     研究目的
     通过对膝骨关节炎大鼠针刀干预前后局部组织形态学的观察,痛阈的观测,中枢神经系统内疼痛相关物质的检测分析,研究寻找针刀松解法对膝骨关节炎疼痛缓解的作用机制,探求其对中枢镇痛作用的影响方式,阐释镇痛机理,为验证针刀疗法的有效性提供客观依据。
     研究方法
     将清洁级3月龄健康SD大鼠80只(雌雄各半)随机分为空白组、模型组、针刀组、电针组,应用木瓜蛋白酶关节内注射的方法制备膝骨关节炎模型。针刀组、电针组于造模第36d开始进行治疗干预,针刀组每周干预1次,电针组每周干预3次(隔日一次),共三周。以热辐射法测定大鼠甩尾反射潜伏期,观察大鼠痛阈变化;光镜观察大鼠局部组织的病理表现;放免法测定脊髓及脑内各水平的P物质(SP)、亮-脑啡肽(L-ENK)、p-内啡肽(p-EP)、八肽胆囊收缩素(CCK-8)含量,酶免法测定脊髓及脑内各水平的5羟色胺(5-HT)、去甲肾上腺素(NE)、多巴胺(DA)含量,观察针刀松解法对疼痛相关神经肽及单胺类神经递质的调节作用。
     研究结果
     1.模型组的痛阈值在各周均比正常组低且具有显著的统计学意义(P<0.01,P<0.05);针刀组和电针组大鼠从治疗开始后痛阈有所提高且与模型组相比有显著性差异(P<0.01,P<0.05);针刀组的痛阈在第二次治疗后明显提高,且提高幅度大于电针组,二者的差值具有极显著的统计学意义(P<0.01)
     2.肉眼观察见模型组关节囊明显增厚,软骨色泽变暗、表面粗糙,可见软骨下骨裸露及骨赘形成。针刀松解法、电针干预能减轻关节囊增厚程度,抑制骨赘的生成。
     3.光镜下见模型组关节结构改变、关节间隙狭窄;关节腔内可见脱落的软骨及滑膜组织;关节软骨出现明显的退变,细胞可见变性、坏死,各层细胞排列紊乱无序;滑膜组织充血水肿,毛细血管增生,可见炎性细胞浸润及血管翳。针刀松解法、电针干预能减少炎性细胞的浸润,降低软骨的破坏程度,维持关节结构的正常。
     4.在脊髓及丘脑内,针刀组SP水平与空白组相比有增加明显,二者差异显著(P<0.01,P<0.05);在下丘脑针刀组的SP水平比模型组极明显降低,二者差异有显著的统计学意义(P<0.01)。在脊髓水平,针刀组的L-ENK、β-EP含量比空白组明显增加(P<0.01),在中脑针刀组的L-ENK,β-EP含量比模型组明显降低(P<0.01)。在脊髓及中脑水平,针刀组的CCK-8含量比模型组明显降低(P<0.01,P<0.05)。电针组与针刀组的指标变化趋势大致相同,提示针刀松解法,电针干预可良性调节脊髓和脑内神经肽的水平,使其更接近正常水平。
     5.与模型组相比,针刀松解法干预后大鼠脊髓及下丘脑水平的5-HT含量增加明显(P<0.05)。与模型组相比针刀松解法干预后大鼠脊髓组织的NE含量增加明显(P<0.05),而在脑内NE含量呈下降趋势。在中脑模型组DA含量较空白组明显升高(P<0.01),针刀组与空白组之间无显著性差异(P>0.05)。电针组与针刀组的指标变化趋势大致相同,提示针刀松解法、电针干预可良性调节脊髓和脑内单胺类神经递质的水平,纠正上述物质的合成和代谢失衡。
     研究结论
     针刀松解法具有镇痛作用,通过本次研究可以发现针刀松解法对膝骨关节炎大鼠中枢镇痛作用的影响有以下特点:①针刀松解法对中枢内的镇痛相关物质(神经肽和单胺类神经递质)均有良性调节作用;②针刀松解法的良性调节作用同时发生在脊髓及脊髓以上水平,脊髓水平的作用更为明显;③针刀松解法对疼痛的调节与其对单胺类神经递质与阿片肽系统代偿机制的影响有关。
     中枢镇痛相关物质的调节方面,本次结果很难体现针刀松解法与电针疗法的区别,无法判定两种治疗方法的优劣。但在痛阈观察方面针刀组的效果要好于电针组,这不但与中枢镇痛相关物质的调节有关,更和局部炎症及组织破坏程度的抑制相关。在治疗次数上针刀治疗次数明显少于电针治疗,这更符合临床患者治疗的需要。
Osteoarthritis (OA) is a very common osteoarthropathy worldwide with high disability rate, and is of great concern to medical institutions due to the impact it has on patients' life, and social activities.2000 World Health Organization Assembly declared 2000-2010 the ten years of Osteoarthritis prevention and cure. In 2002, China Ministry of Health and Chinese Medical Association declared 2002-2012 "the ten years for healthy bones and joints of Chinese". Knee joint is susceptible to OA. Knee Osteoarthritis (KOA) is characterized mainly by knee joint pain, stiffness, and limitation to movement. Patients often seek treatment because of joint pain.
     Acupotomy lysis proved eutherapeutic in the treatment of KOA. The research on acupotomy is developing toward basic fields. This project relies on Acupotomy Lysis Basic Research under Specialized Traditional Chinese Medicine Programs funded by National Basic Research Program of China (973 Program). Through animal testing, this project studies how acupotomy lysis eases pain, and its central mechanism for the purpose of providing factual evidence to confirm the effectiveness of acupotomy.
     Objective
     Through observing the morphology of local tissues of rats with KOA, measuring threshold of pain, and detecting and analyzing pain-related substances in central nervous system before and after acupotomy intervention, this project studies how acupotomy lysis eases KOA pain, explores how it influences central analgesia function, and elucidates its pain alleviation mechanism, for the purpose of providing factual evidence to confirm the effectiveness of acupotomy.
     Methods
     Divide 80 three-month-old healthy laboratory SD rats (equal between genders) randomLy into normal control group, model group, acupotomy lysis group, and electro-acupuncture group. Prepare KOA models by injecting papain solution into knee joint cavities of rats. Start treating acupotomy group and electro-acupuncture group rats on 36d after modeling. Treat acupotomy group once a week, electro-acupuncture group three times a week (once every other day), for three weeks. Measure the tail flick latency of rat using heat radiation to observe the variation of the pain threshold of rats. Observe the pathology of local tissues of rats through optical microscope. Measure the content of SP, I-ENK, (3-EP, and CCK-8 in tissues in spinal cord and brain using radioimmunOAssay. Measure the content of 5-HT, NE, and DA in tissues in spinal cord and brain using enzyme immunOAssay. Observe the regulatory function of acupotomy lysis on pain-related neuropeptide and monOAmine neurotransmitter.
     Result
     1. Pain threshold of model group is much lower than normal control group throughout the testing (P<0.01, P<0.05). Pain threshold of acupotomy group and electro-acupuncture group has risen after treatment starts, and is significantly different than model group (P<0.01, P<0.05). Pain threshold of acupotomy group rises sharply after the 2nd treatment, and rises more than electro-ecupuncture group does (P<0.01)
     2. There are to the naked eye noticeable thickening of articular capsule, darkening and roughness of cantilage, exposed subchondral bone, and formation of osteophyte of rats in model group. Acupotomy lysis can reduce articular capsule thickening, and inhibit the forming of osteophyte.
     3. Changed joint structure and narrow joint space are seen through optical microscope. Inside joint cavity are found cartilage and synovial membrane that have come off. Joint cartilage is found with conspicuous degeneration. Denaturation and necrosis of cells is seen. Cells in different layers are in disorder. Synovial membrane is congestive and edematous. Capillary is hyperplastic. Inflammatory cell infiltration and pannus are found. Acupotomy lysis and electro-acupuncture can reduce inflammatory cell infiltration and damage to cartilage such that normal joint structure is maintained.
     4. In respect of SP content in spinal cord and thalamus, acupotomy group has risen sharply compared with normal control group(P<0.01, P<0.05). In respect of SP content in hypothalamus, acupotomy group is significantly lower than normal control group (P<0.01). In respect of I-ENK andβ-EP content in spinal cord, acupotomy group has risen sharply compared with normal control group (P<0.01). In respect of I-ENK andβ-EP content in midbrain, acupotomy group is significantly lower than normal control group (P<0.01). In respect of CCK-8 content in spinal cord and midbrain, acupotomy group is significantly lower than normal control group (P<0.01, P<0.05). The indices of acupotomy group and electro-acupuncture group change with similar trends, that shows acupotomy lysis and electro-acupuncture can adjust in a favorable way the neuropeptide content in spinal cord and brain to make them closer to normal level.
     5. The 5-HT content in spinal cord and hypothalamus of rats treated with acupotomy lysis has risen sharply compared with that of normal control group rats (P<0.05). Compared with normal control group, the NE content in spinal cord tissues of rats treated with acupotomy lysis has risen sharply (P<0.05) NE content in brain shows a downward trend. In respect of midbrain DA content, model group has risen sharply compared with normal control group (P<0.01). There is no significant difference between acupotomy group and normal control group The indices of acupotomy group and electro-acupuncture group change with similar trends, that shows acupotomy lysis and electro-acupuncture can adjust in a favorable way the monOAmine neurotransmitter content in spinal cord and brain to correct their anabolism imbalance.
     Conclusion
     Acupotomy lysis functions to ease pain. Through this project it can be found that acupotomy lysis influences pain alleviation function of the central nervous system of rats with KOA with the following characteristics:①acupotomy lysis functions to adjust in a favorable way the pain-alleviation-related substances (neuropeptide and monOAmine neurotransmitter) in central nervous system;②the favorable adjustment function of acupotomy lysis exists in both spinal cord and the tissues above it, though in spinal cord it is more conspicuous;③the adjustment by acupotomy lysis to KOA induced pain reflects compensatory mechanism of monOAmine neurotransmitter and opioid peptide system.
     It is difficult to conclude from the findings of this project either of acupotomy lysis and electro-acupuncture is more effective in adjusting pain-alleviation-related substances in central nervous system, so it cannot be determined which therapy is better. Observation in this project shows that acupotomy lysis is more effective than electro-acupuncture in raising pain threshold, that might be related to the adjustment to pain-alleviation-related substances in central nervous system, and the inhibition of inflammation of and damage to local tissues. Acupotomy lysis is more convenient for patients since it is administered far less frequently than electro-acupuncture.
引文
[1]曾庆徐,黄少弼.症状性骨关节炎临床和流行病学探讨[J].中华内科杂志,1995,34(20):88.
    [2]徐苓,Michael C Nevitt, Yuqing Zhang,等.北京城区老年人膝,髋和手骨关节炎患病率及其与美国白人患病率的比较研究[J].中华医学杂志,2003,83(14):1206-1209.
    [3]李宁华,张耀南,张毅,等.国内六大行政区域六城市中老年人群膝关节骨性关节炎患病危险因素比较[J].中国组织工程研究与临床康复,2007,11(39):7758-7760.
    [4]荣杰生,陶天遵,陶树清,等.高寒地区城市汉族人群膝骨关节炎情况调查[J].中国骨质疏松杂志,2007,13(10):723-726.
    [5]顾明士,杨军,金哲峰,等.社区中老年人膝骨关节炎发病趋势的分析[J].中医药临床杂志,2005,3:246-247.
    [6]曾庆馀,许杰洲,林秋强,等.原发性症状性骨关节炎805例临床分析[J].中华风湿病学杂志,1998,2(1):40-43.
    [7]J. P. Jackson, W. Waugh. Surgery of the Knee Joint. Chapman and HallLtd[M]. London,1984,2:20.
    [8]管剑龙,韩星海.中国骨关节炎十年[M].第二军医大学出版社,2006,1.
    [9]李文顺,沈冯君,易洪城.膝骨性关节炎的病因病理研究[J].贵阳中医学院学报,2002,24(4):8-10.
    [10]康思宁,刘强.骨关节炎病理过程与关节软骨特性的改变[J].中华关节外科杂志(电子版),2007,1(4):275-278.
    [11]Ratcliff A, Fryer P R, Hardingham T E. The distribution of proteoglycans in articular cartelage[J]. J Hischem Cytochem,1984,32(2):193-201.
    [12]Wirth C, Rudert M.促进关节软骨生长的方法[J].中医正骨,1998,10(5):55-56.
    [13]黄异飞,敖英芳,王梅.髁间侧壁软骨组织学结构特点及其临床意义[J].中国运动医学杂志,2003,22(6):573-575.
    [14]翁习生,任玉珠.骨性关节炎病因研究进展[J].中华骨科杂志,1996,16:60.
    [15]陈连旭,余家阔,于长隆,等.大鼠,兔和人关节软骨组织形态学的比较[J].中国组织工程研究与临床康复,2007,11(41):8230-8233.
    [16]赵丹慧,张艳,薛延等.豚鼠原发性骨性关节炎超微结构与生化改变的动态观察[J].中华手外科杂志,1999,15(3):180-182.
    [17]唐勇,姜杰,周永红,等.骨炎定对兔实验性膝骨关节炎关节软骨的组织病理学影响[J].四川中医,2004,22(1):23-25.
    [18]邢国胜,金鸿宾,王志彬,等.痹祺胶囊对兔骨性关节炎关节软骨破坏的干预作用[J].中国中西医结合外科杂志,2009,15(5):547-551.
    [19]孙嘉利,范建中.兔膝关节骨性关节炎的模型制作及组织病理学[J].中国康复,2005,20(2):78-80.
    [20]吴向阳,侯筱魁.正常力学环境下急性关节软骨损伤修复机制的电镜观察[J].实用医学杂志,2007,23(14):2141-2143.
    [21]Shapiro F, Koide S, Glimcher M J, et al. Cell origin and differentiation in the repair of full-thickness defects of articular cartilage [J]. J Bone Joint Surg,1993, 75 (4):532-553.
    [22]Verzijl N, DeGroot J, Ben ZC, et al. Crosslinking by advanced glycation end products increases the stiffness of the collagen network in human articular cartilage: a possible mechanism through which age is a risk factor for Osteoarthritis[J]. Arthritis Rheum 2002,46(1):114-123.
    [23]Aigner T, McKenna L. Molecular pathology and pathobiology of osteOArthritic cartilage[J]. Cell Mol Life Sci 2002,59(1):5-18.
    [24]陈崇伟,卫小春.关节软骨浅表层的透射电镜观察[J].山西医科大学学报,2005,36(1):44-46.
    [25]卫小春,陈崇伟,郝一勇,等.骨关节炎关节软骨的透射电镜观察[J].中国药物与临床(骨科专辑),2003,3:54-57.
    [26]Wei XC. Maturation-dependent normal and injury-induced change in rabbit knee articular cartilage [J]. Linkoping:Linkoping University,1998,1-13.
    [27]Heraud F, Heraud A, Harmand MF. Apoptosis in normal and ost-eOArthritis human articular cantilage[J]. Ann Rheum Dis,2000,59:959-965.
    [28]Hashimoto S, Setareh M, Ochs RL, et al. Fas/Fas ligand expression and induction of apoptosis in chondrocytes. Arthritis Rheum,1997,40(10):1749-1755.
    [29]Blanco FJ, Guitan R, Vaspuez Martul E, et al. Osteoarthritischondrocytes die by apoptosis[J]. Arthritis Rheum,1998,41 (2):284-289.
    [30]胡建华,黄公怡,黄尚志,等.骨关节炎软骨细胞调控基因的研究[J].中华外科杂志,2000,38(4):266-268.
    [31]程爱新,王莺,马大龙,等.程序化死亡基因5(PDCD5)在骨关节炎软骨中的表达及意义[J].北京大学学报(医学版),2003,35(5):481-484.
    [32]Hashimoto S, Ochs RL, Komiya S, et al. Linkage of chondrocyte apoptosis and cartilage degradation in human Osteoarthritis[J]. ArthritisRheum,1998,41 (9): 1632-1638.
    [33]Aigner T, Kurz B, Fukui N, et al. Curr Op in Rheumatol,2002,14 (5): 5782-5841.
    [34]Blaw FJ, Guistian R, Vazguez ME, et al. Osteoarthritis chonodrocytes did by apoptosis:A possible pathway for Osteoarthritis pathology[J]. Arthritis Rheum, 1998,41 (2):284-289.
    [35]Kim HA, Lee YJ, Seong SC, et al. Apoptotic chondrocyte death in human Osteoarthritis[J]. J Rheum,2000,27(2):455-462.
    [36]Pelletier JP, Fernandes JC, Jovanovic DV, et al. Chondrocyte death in experimental Osteoarthritis is mediated by MEK 1/2 and p38 pathways:role of COX-2 and iNOS[J]. Journal of Rheumatology,2001,28(11):2509-2519.
    [37]Huber M, Trattnig S, Lintner F. Anatomy, biochemistry, and physiology of articular cartilage[J]. Invest Radio,2000,35:573-580.
    [38]彭丹,孙材江.实验性骨关节病中软骨细胞的凋亡[J].湖南医科大学学报,1999,24(5):415-417.
    [39]王庆蓉,官颖鹏,邵卫.软骨细胞在膝骨性关节炎中的超微结构改变[J].电子显微学报.2000,19(6):820-824.
    [40]Hashimoto S, Takahashi K, Amiel D, et al. Chondrocyte apoptosis and nitric oxide production during experimentally induced Osteoarthritis[J]. Arthritis Rheum, 1998,41 (7):1266-1274.
    [41]Adams CS, Horton WE Jr. Choondrocyte apoptosis increases with ageing the articular cartilage of adult animals[J]. AnatRec,1998,250 (4):418-424.
    [42]解志杰,许建中.IGF-1和TGF-β对幼年及成年兔关节软骨细胞增殖和代谢的作用[J].第三军医大学学报,2001,23(6):670-672.
    [43]Lotz M, Hashimoto S, Kuhn K. Osteo Cart,1999,7(4):389-391.
    [44]Kobayashi K, Mishima H, Hashimoto S, et al. J Orthop Res,2001,19: 8022-8081.
    [45]茅文斌,邵增务.一氧化氮与骨性关节炎研究进展[J].国际骨科学杂志.2006,27(4):232-234.
    [46]贾堂宏,张佐伦.细胞凋亡与关节破坏[J].山东医药.2002,42(17)68-69.
    [47]王卓,王连唐.骨关节炎病理改变及其研究进展[J].国外医学内科学分册,2005,32(7):312-214,319.
    [48]刘淑芳,李莹辉,徐团才.骨性关节炎的生理及病理变化[J].中国临床康复,2004,8(5):938-939.
    [49]戴颖,黄涛,白希壮.关节软骨中胶原的分布及在骨关节炎中的变化[J].国外医学骨科学分册,2004,25(2):101-104.
    [50]郭秦炜,田得祥,敖英芳.骨性关节炎关节软骨中Ⅰ型,Ⅱ型,Ⅲ型及X胶原的分布[J].中国运动医学杂志2002,21(3):228-231.
    [51]陈崇伟,卫小春,向川,等.骨性关节炎关节软骨内Ⅰ,Ⅱ,Ⅲ型胶原表型的实验研究[J].山西医科大学学报,2006,37(3):248-251.
    [52]陈崇伟,卫小春,杨自权,等.伸膝制动骨关节炎动物模型软骨内胶原变化的观察[J].中华风湿病学杂志,2003,7(6):332-335.
    [53]马春辉,蔡国平,阎作勤.Ⅱ型胶原在骨关节炎软骨细胞中的表达[J].复旦学报医学版,2009,36(6):734-736.
    [54]Admas ME, Maty as JR, Huang D, et al. Expression of proteoglycans and collegen in the hypertrophic phase of experimental Osteoarthritis[J]. Rheumatol Suppl1995,43:94-97.
    [55]钱善华,葛世荣.天然关节软骨的液体质量分布特征[J].生物骨科材料与临床研究,2009,6(1):46-48.
    [56]Thomas J T, Ayad S, Grant M E, et al. Cartilage collagens:strategies for the study of their organisation and expression in extracellular matrix[J]. Ann Rheum Dis,1994,53 (8):488-496.
    [57]卫晓恩,庄志杰,石印玉,等.不同年龄段骨关节炎患者关节滑液中基质蛋白多糖的变化[J].中国临床康复,2005,9(30):138-139.
    [58]卫晓恩,杨庆铭,邓廉夫,等.骨关节炎体液中蛋白多糖代谢改变的实验研究[J].中华风湿病学杂志,2002,6(6):445-446.
    [59]卫晓恩,杨庆铭,邓廉夫,等.骨关节炎软骨基质蛋白多糖变化的实验研究[J].中华风湿病学杂志,2002,6(1):25-27.
    [60]管剑龙,韩星海.中国骨关节炎十年[M].第二军医大学出版社,2006,37-40.
    [61]Johansen JS, Olee T, Price PA, et al. Regulation of YKL-40 production by human articular chondrocytes[J]. Anthritis Rheum,2001,44:826-837.
    [62]Volck B, Johansen JS, Stoltenberg M, et al. Studies on YKL-40 in knee joints of patients with rheumatoid arthritis dnd Osteoarthritis:involvement of YKL-40 in the joint pathology[J]. Osteoarthritis Cartilage,2001,9:203-214.
    [63]Masashi K, Yukiharu H, Seiji K, et al. Concentration and localization of YKL-40 in hip joint diseases. J Rheumatol,2001,28:341-345.
    [64]张洪,张阳德,王大平等,糖蛋白YKL-40在骨关节炎中的表达[J].中国现代医学杂志,2007,17(24):2994-2995.
    [65]Decuninck F, Gaufillier S, Bonnaud A, et al. YKL-40(cartilagegp-39) induces proliferative events in cultured chondrocytes and synoviocytes and increases glycosaminoglycan synthesis in chondrocytes[J]. Biochem Biophys Res Commun, 2001,285:926-931.
    [66]TakahashiM, NaitoK, AbeM, et al. Relationship between radiographic grading of Osteoarthritis and the biochemicalmarkers for arthritis in knee Osteoarthritis[J]. Arthritis Res Ther,2004,6:208-212.
    [67]鱼云霞,赵月霞,王芳,血清YKL-40检测对骨性关节炎的早期诊断价值[J].宁夏医学杂志,2009,31(3):269-270.
    [68]王国金,卫小春,郝一勇,YKL-40在骨关节炎发病中的作用[J].中华风湿病学杂志,2006,10(1):52-55.
    [69]陈百成,王晓峰,张静,等.膝关节骨关节炎滑膜中神经生长因子和P物质水平测试与观察[J].中华骨科杂志,2003,23(3):156-160.
    [70]吴林生,金嫣莉.膝痛[M].人民卫生出版社,1997,351.
    [71]王学谦,娄思权,侯筱魁,等主译.骨关节炎--诊断与治疗(第三版)[M].天津科技翻译出版公司,2005,66.
    [1]吴林生,金嫣莉.膝痛[M].北京:人民卫生出版社,1997,347.
    [2]张荣,李峰,王常海,等.经筋理论在膝关节骨性关节炎发病机制及治疗中的作用[J].中国康复医学杂志,2007,22(7):644-646.
    [3]郝军,高文香,邹春雨. “筋为骨用”理论方法综合治疗膝骨性关节炎80例临床观察[J].中医杂志,2009,50(2):139-141.
    [4]王跃辉,韩清民,李钊,等.生物力学因素在骨关节炎诊疗体系中的价值探讨--骨关节炎经筋诊疗思路浅谈[J].中国中医骨伤科杂志,2010,18(1)68-70.
    [5]周仲瑛.中医内科学[M].北京:中国中医药出版社,2003,481.
    [6]王新华.中医基础理论[M].北京:人民卫生出版社,2001,184.
    [7]国家技术监督局中医临床诊疗术语疾病部分[S].北京:中国标准出版社,1997:58.
    [8]国家技术监督局中医临床诊疗术语证候部分[S].北京:中国标准出版社,1997:51.
    [9]周杰,顾非.膝关节骨性关节炎中医治疗概况[J].当代医学,2010,16(9):149-151.
    [10]彭江云,李兆福,刘维超,等.骨痹中医诊疗方案介绍[J].云南中医学院学报,2009,33(6):43-47.
    [11]黄俊卿.论《诸病源候论》的痹病理论体系[J].河南中医药学刊,1997,(6): 2.
    [12]肖林蓉,郑红.明清医家论治骨痹(骨关节炎)临床理论的发展[J].中医文献杂志,2003, (2):10.
    [13]杨锦华,曹惠英,冯仲锴,等.原发性膝关节骨关节炎中医证候流行病学调查[J].中医正骨,2005,17(7):19-22.
    [14]刘向前,姚共和,李建斌,等.膝关节骨关节炎中医住院病历中医证候诊断回顾性分析[J].湖南中医学院学报,2004,10,24(5):30-32.
    [15]王定,史晓林,李文庆,等.膝骨性关节炎中医药治疗的研究进展[J].2008,16(4): 65-67.
    [16]王富拴,贾瑞先,王跃辉.补肾活血方治疗膝骨关节炎60例[J].辽宁中医杂志,2010,37(3):477-478.
    [17]刘玉兰.中药治疗骨性关节炎疼痛136例[J].江苏中医,1997,18(6)26.
    [18]孙年祥.补肾活血法治疗骨关节炎30例[J].实用中医药杂志,1997,13,(6): 16.
    [19]杨金莲,徐兰凤.针灸治疗膝骨关节炎临床研究进展[J].广西中医学院学报,2008,11(2):67-69.
    [20]李秀彬.隔物温和灸治疗膝骨关节炎疗效观察[J].上海针灸杂志,2010,29(3): 178-180.
    [21]吕正祥,陈伟峰.舒筋活血药加中药外敷治疗膝骨性关节炎150例疗效评价[J].辽宁中医药大学学报,2010,12(3):11-12.
    [22]蒙昌荣,李滋平,樊莉,等.针刺治疗不同证型膝骨性关节炎的临床研究 [J].辽宁中医杂志,2008,35(7):1083-1084.
    [23]王朝兴,张少杰.针刺膝阳关,曲泉为主治疗膝骨关节炎[J].医学信息,2009,22(3):414.
    [24]钟宾谟,林国华.温针治疗膝关节骨性关节炎的临床疗效观察[J].按摩与导引,2004,20(8):16-18.
    [25]唐长华,李玉富.解毒益肾法治疗膝骨性关节炎临床研究[J].中华中医药学刊,2010,28(1):217-219.
    [26]宋绍亮.张鸣鹤主任医师治疗关节病的经验[J].山东中医杂志,1991,10(13):44.
    [27]白建兰,张殿玺.血府逐瘀胶囊及玻璃酸钠联合用药治疗膝关节骨性关节炎疗效观察[J].中国中医骨伤科杂志,2010,18(3):15-17.
    [28]陆乾人,王晓军,朱卫红.电针加穴位注射治疗膝骨关节炎临床观察[J].上海针灸杂志,2010,29(1):43-44.
    [29]张素梅,夏留忠,朱培罡等,药棒改良疗法配合刺络拔罐治疗膝骨性关节炎68例报告[J].颈腰痛杂志,2010,31(1):75.
    [30]曾红文,聂斌,史琳琳,刺血合火针点刺治疗膝关节骨性关节炎疗效观察[J].中国针灸,2008,28(7):493-495.
    [31]杨嘉珍,黄进,覃一珏.补肾祛寒活络法治疗膝骨关节炎临床观察[J].辽宁中医药大学学报,2009,11(4):144-145.
    [32]樊成虎,张玉昌.陇中中药洗剂治疗膝关节骨性关节炎60例临床观察[J].甘肃中医,2008,21(12):7.
    [33]李茜,朱江.神阙灸配合电针治疗阳虚寒凝型膝骨关节炎疗效观察[J].中国针灸,2008,28(8):565-568.
    [34]任硕.温针灸对侧曲池穴为主治疗膝骨关节炎22例临床观察[J].黑龙江中医药,2010,(1):33-34.
    [35]王少山,张世华,邱红明,等.骨病中西医诊疗学[M].北京:中国中医药出版社,2002,186.
    [36]廖志刚,费兰波.中药熏蒸结合针灸治疗膝骨性关节炎的疗效观察[J].中国中医骨伤科杂志,2010,18(3):27-28.
    [37]鄢卫平.针刺、按摩、中药外敷治疗膝关节骨性关节炎128例[J].甘肃中医,2008,21(11):19.
    [38]谭训香,于晓丽.玻璃酸钠关节腔注射加销针刀剥离治疗膝骨性关节炎[J].中医正骨,2005,17(12):24.
    [39]施红曙.阿是穴为主推拿治疗退行性膝关节炎53例[J].江西中医药,2008,39(309):35-36.
    [40]倪凌.手法治疗膝骨关节病58例[J].中国骨伤,1994,7(2):27-28.
    [41]谢利民.张涛研究员治疗膝关节软骨退行性疾病的手法特点[J].中医正骨,1999,11(5):51.
    [42]田佩洲.带刃针治疗膝骨关节炎81例临床体会[J].山西中医学院学报,2008,9(3):37-38.
    [43]陈小凯.解结针法治疗膝骨关节炎[J].针灸临床杂志,2009,25(9):41-42.
    [44]顾宜宜,熊源胤,易平.经筋齐刺法治疗膝骨关节炎30例临床观察[J].中医药学报,2008,36(3):33-35.
    [45]李辉,周承扬,朱奕.小针刀结合手法治疗膝骨关节炎110例疗效观察[J].长 春中医药大学学报,2009,25(6):891-892.
    [46]胡水荣,尹利华,李万瑶.针刀改善膝骨关节炎症状的临床研究[J].江西医药,2009,44(11):1093-1095.
    [1]朱锦杰.膝关节炎的影像学评估与功能,疼痛及肌力评估的关系[J].国外医学·物理医学与康复学分册,2005,25(3):115-116.
    [2]曾贵刚,张秀芬,权伍成,等.针刀松解法对膝骨性关节炎应力刺激及临床症状的影响[J].中华中医药学刊,2009,27(1):66-68.
    [3]Murat N, Karadam B, Ozkal S, et al. Quantification of papain-induced rat Osteoarthritis in relation to time with the Mankin score[J]. Acta Orthop Traumatol Turc,2007,41 (3):233-237.
    [4]李忠仁.实验针灸学[M].北京:中国中医药出版社,2003,314.
    [5]胡元亮.实验动物针灸手册[M].北京:中国农业出版社,2003,288.
    [6]汪青春,石印玉,沈培芝,等.增龄及运动负荷对C57黑鼠关节软骨影响的组织病理学观察[J].中国骨伤,2000,13(9):517-518.
    [7]侯炜,梁倩倩,何建新,等.鼠类膝骨关节炎模型的研究进展[J].中国中医骨伤科杂志,2009,17(4):64-66.
    [8]刘献祥,李西海,周江涛.改良Hulth造模法复制膝骨性关节炎的实验研究[J].中国中西医结合杂志,2005,25(12):1104-1108.
    [9]白希壮,任继尧.选择性臀肌切断诱发骨关节炎实验模型[J].中华骨科杂志,1994,14(2):118-120.
    [10]Marijnissen AC, Van Roermund PM, TeKoppele JM, et al. The canine'groove' model, compared with the ACLT model of Osteoarthritis[J]. Osteoarthritis Cartilage,2002,10 (2):145-155.
    [11]王贤波,蒋青.大鼠骨性关节炎模型的构建及其稳定性观察[J].中国临床康复,2005,9(10):72-74.
    [12]陈宝兴,丁继华.双后肢大白鼠的骨关节病实验研究[J].中华骨科杂志,1987,7:296.
    [13]石绍华,刘立建,卓仁禧.木瓜蛋白酶固定化研究进展[J].湖北省卫生职工医学院学报,1998,2:55-58.
    [14]Havdtup T, Telhag H, et al. Papain induced changes in the knee joints of adult rabbits[J]. Acta Orthop Scand,1977,48:143.
    [15]江捍平,王大平.骨关节炎动物模型[J].中国现代医学杂志,2004,14(6):153-154,156.
    [16]翟吉良,翁习生,邱贵兴.骨关节炎动物模型的建立及选择[J].中国矫形外科杂志,2007,15(11):843-845.
    [17]张荣,李峰,王常海,等.经筋理论在膝关节骨性关节炎发病机制及治疗中的作用[J].中国康复医学杂志,2007,22(7):644-646.
    [18]郝军,高文香,邹春雨. “筋为骨用”理论方法综合治疗膝骨性关节炎80例临床观察[J].中医杂志,2009,50(2):139-141.
    [19]王跃辉,韩清民,李钊,等.生物力学因素在骨关节炎诊疗体系中的价值探讨--骨关节炎经筋诊疗思路浅谈[J].中国中医骨伤科杂志,2010,18(1):68-70.
    [20]朱汉章.针刀医学[M].北京:中国中医药出版社,2004,137,141.
    [21]金惠生,金安,金河,等.骨质增生症的非手术治疗[M].北京:中国医药 科技出版社,1997,365-366.
    [22]谭训香,于晓丽.玻璃酸钠关节腔注射加销针刀剥离治疗膝骨性关节炎[J].中医正骨,2005,17(12):24.
    [23]嵇波,刘清国,符永鋆,等.针刀松解法,电针对膝关节骨关节炎兔IL-1,IL-6, TNF-a含量影响的比较[J].中国病理生理杂志,2009,25(6):1165-1168.
    [24]俞杰,明顺培,张秀芬,等.针刀疗法对兔膝骨关节炎关节液中IL-1β, IL-6, TNF-a水平的影响[J].中国中医骨伤杂志,2002,10(4):15-18.
    [25]童娟,余杰,陈健雄,等.针刀疗法治疗膝骨关节炎实验研究[J].国际医药卫生导报,2003,9(8):4-5,7.
    [26]刘清国,嵇波,覃蔚岚,等.针刀松解法对骨性关节炎兔血清基质金属蛋白酶3和13含量的影响[J].针刺研究,2008,33(5):336-339.
    [27]何新芳,明顺培,俞杰,等.针刀疗法对膝骨关节炎兔关节软骨细胞凋亡的影响[J].辽宁中医杂志,2006,33(7):894-895.
    [28]章瑛,李家邦,周锦财,等.实验性膝关节病与血清c-反应蛋白的变化及局部松解的影响[J].中国骨与关节损伤杂志,2005,20(8):539-540.
    [29]章瑛,李家邦,李霞玲,等.松解疗法对实验性骨性关节炎组织病理学的影响[J].中国中医骨伤杂志,2005,13(4):5-6,10.
    [30]章瑛,李家邦,周江南,等.膝关节退行性变动物模型SOD, MDA的变化及局部松解对其影响[J].中国医师杂志,2005,9(8):1056-1057.
    [31]章瑛,周锦财.松解针治疗家兔膝关节退行性变的实验研究[J].湖南中医学院学报,2001,21(3):56-58.
    [32]郭长青,刘乃刚,李晓泓,等.针刀松解法对第三腰椎横突综合征大鼠血管活性物质的影响[J].针刺研究,2007,32(5):323-326.
    [33]卢敏,谢进,戴致波.小针刀对兔骨折愈合影响的实验研究[J].湖南中医药大学学报,2007,27(4):70-72.
    [34]卢敏,戴致波,谢进,等.小针刀治疗对骨折愈合血管内皮细胞生长因子表达及血清无机盐和碱性磷酸酶影响的实验研究[J].中国中医骨伤科杂志,2007,15(6):9-12.
    [35]赵斌,刘玉倩,王海涛.小针刀治疗肌肉损伤的组织学和生物力学研究[J].体育科学,2004,24(9):28-31.
    [36]徐卫东,吴岳嵩,张春才.骨关节炎的诊断与治疗[M].上海:第二军医大学出版社,2004,33.
    [37]王学谦,娄思权,侯筱魁,等主译.骨关节炎--诊断与治疗(第三版)[M].天津:天津科技翻译出版公司,2005,56.
    [38]Kuijper A, van der Groep P, van der Wall E, et al. Breast Caner Res[M].2005, 7(5):808-818.
    [39]李文顺,沈冯君,易洪城.膝骨性关节炎的病因病理研究[J].贵阳中医学院学报,2002,24(4):8-110.
    [40]Altman RD. Pain relief in Osteoarthritis; the rationale for combination therapy[J]. J Rheumatol,2004,31 (1):5-7.
    [41]Dougados M. Monitoring Osteoarthritis progression and therapy[J]. Osteoarthritis Cartilage,2004,12 (A):S55-S60.
    [1]Murat N, Karadam B, Ozkal S, et al. Quantification of papain-induced rat Osteoarthritis in relation to time with the Mankin score [J]. Acta Orthop Traumatol Turc,2007,41 (3):233-237.
    [2]李忠仁.实验针灸学[M].北京:中国中医药出版社,2003,314.
    [3]胡元亮.实验动物针灸手册[M].北京:中国农业出版社,2003,288.
    [4]张吉.针灸镇痛机制与临床[M].北京:人民卫生出版社,2002,180.
    [5]方富贵,章孝荣.P物质的研究进展[J].动物医学进展,2005,26(1):6-8.
    [6]季华,韩曙,郑轶.P物质和P物质受体在小鼠胚胎发育期脑内的表达[J].解剖学报,2006,37(5):578-583.
    [7]陶克,陈璧,胡大海,等.NK-1受体非肽类拮抗剂L-703,606对严重烫伤大鼠早期P物质免疫反应阳性神经的影响[J].西北国防医学杂志,2007,28(1):56-59.
    [8]李云庆,王智明.大鼠脊髓P物质受体分布的免疫细胞化学研究[J].神经解剖学杂志,1995,11(3):215-220.
    [9]Foster AP, Cunningham FM. Substance P induces activeation, adherence and migrateon of equine eosinophils[J]. J Cet Pharmacol Ther,2003,26 (2):131-138.
    [10]Millan MJ. Descending control of pain[J]. Progress in Neurobiology.2002, 66:355-474.
    [11]翁恩琪.痛与镇痛[M].上海:上海科学技术出版社,1987,164.
    [12]朱建军.脊髓P物质在电针镇痛中作用的研究进展[J].南通大学学报(医学版),2007,27(3):228-230.
    [13]胡国兴,钟敏,曾因明.鞘内注射新斯的明对手术切口引起的大鼠脊髓背角P物质表达的影响[J].中国疼痛医学杂志,2005,11(2):96-99.
    [14]夏智群,王国林.神经生长因子在炎性疼痛中的作用[J].天津医药,2006,34(10):719-721.
    [15]杜小正,秦晓光,尹少兰,等.传统“热补”针法对实验室关节炎兔痛阈及脊髓SP含量的影响[J].中医研究,2006,19(1):12-15.
    [16]张恒,周占松,刘丽梅,等.P物质对脊髓星形胶质细胞活化和炎性因子IL-1β, TNF-a分泌的影响[J].第三军医大学学报,2006,28(7):681-684.
    [17]罗非,李楠,田津斌,等.反复电针对单发佐剂关节炎模型大鼠脊髓P物质,八肽胆囊收缩素及甲硫氨酸脑啡肽样免疫活性物质自发释放的影响[J].中国疼痛医学杂志,1996,2(3):169-175.
    [18]盛佑祥,杨万章,吴芳.电针对炎症痛镇痛机制的实验研究进展[J].上海针灸杂志,2006,25(8):47-50.
    [19]Kream RM. Substance P markedly potentiates the antinociceptive effects of morphine sulfate administered at the spinal leve[J]l. Proc Natl Acad SCI USA, 1993,90:3564.
    [20],边景檀.脊髓中P物质参与电针镇痛的研究[J].生理科学进展,1995,26(4):325-328.
    [21]沈上,边景檀,田津斌,等.电针引起脊髓P物质释放的频率依赖性[J].生理学报,1996,48(1):89-93.
    [22]李辉,李云庆.内源性阿片肽参与痛信息调控的机制[J].神经解剖学杂志,2004,20(2):191-196.
    [23]王晓琳,陈涛,李云庆.小鼠中脑导水管周围灰质下行投射的SP能终末与中缝大核内SP受体阳性神经元的突出联系[J].神经解剖学杂志,2007,23(3):283-287.
    [24]周仲福,谢国玺,韩济生.P物质在家兔中脑导水管周围灰质通过释放脑啡肤引起镇痛[J].科学通报,1985,30:69-73.
    [25]李积胜,闰国平,王大宁.P物质在大鼠中缝大核中参与痛觉调制的机制探讨[J].武警医学院学报,2002,11(4):228-231.
    [26]Commons KG, Valeniino RJ. Cellular basis for the effects of substance P in the periaqueductal gray and dorsal raphe nucleus[J]. Comp Neurol,2002,447(1): 82-97.
    [27]闫国平,李积胜.P物质参与大鼠外侧网状核痛觉调制的可能机制[J].基础医学与临床,2003,23(5):568-569.
    [28]展淑琴,赵晏,王会生,等.电针对大鼠脑内P物质表达的影响[J].针刺研究,2002,27(1):33-36.
    [29]林亚平,彭艳,易受乡,等.不同电针频率刺激对胃扩张疼痛大鼠下丘脑内P物质,p-内啡呔表达的影响[J].针刺研究,2009,34(4):252-257.
    [30],胡波,刘琳,郭长青,等.针刀松解法对第三腰椎横突综合征大鼠下丘脑与脊髓P物质,八肽胆囊收缩素含量的影响[J].针刺研究,2008,33(1)22-25.
    [31]崔仁麟.低位脑干和脊髓P物质在针刺镇痛作用中的神经生化研究[J].针刺研究,1994,19(4):45-47.
    [32]史玉兰,张金平.脑啡肽的研究进展[J].河北医科大学学报,2007,28(2):148-150.
    [33]梁映霞.疼痛相关受体和离子通道及其应用[J].广东医学,2008,29(1):154-155.
    [34]王蕾,欧可群.内源阿片肽的研究进展[J].四川解剖学杂志,2000,8(4):227-230.
    [35]杜小正,秦晓光,赵彬元,等.传统“热补”针法对实验性关节炎家兔的镇痛效应及脑脊液中β-EP, CCK-8含量的影响[J].针刺研究,2006,31(2):86-89.
    [36]黄泳.纳甲法针刺对佐剂性关节炎家兔亮氨酸脑啡肽的影响[J].中国临床康复,2004,8(30):6676-6677.
    [37]梁宜,吴翔.针灸治疗类风湿性关节炎镇痛机制研究进展[J].中医药临床杂志,2004,16(5):509-510.
    [38]张露芬,闫明茹,程金莲,等.针刺对早期佐剂性关节炎模型大鼠血浆,下丘脑,垂体及淋巴结β-EP水平的影响[J].北京中医药大学学报,2007,30(1):70-73.
    [39]Huifu G. Brain substractes activated by electrOAcupuncture of different frequencies (Ⅰ):comparative study on the expression of oncogene c-fos and genes coding fos three opioid peptides[J]. Molecular Brain Res,1996,43:157.
    [40]王一菱,吴景兰,金辉.电针对疼痛患者血浆及小鼠脊髓甲硫氨酸脑啡肽,强啡肽及痛阈的影响[J].河南医科大学学报,2001,36(4):425-426.
    [41]梁繁荣,刘雨星,罗荣,等.不同针法对急性佐剂性关节炎大鼠下丘脑β-内啡肽的后效应观察[J].中国针灸、,2004,24(11):782-284.
    [42]付戈,梁繁荣,陶巧林.不同针法对佐剂性关节炎大鼠下丘脑镇痛效应比较[J].上海针灸杂志,2005,24(5):38-41.
    [43]梁繁荣,刘雨星,罗荣,等.不同针法镇痛后效应与下丘脑β-内啡肽机制研究[J].成都中医药大学学报,2004,27(3):22-25.
    [44]梁繁荣,刘雨星,陈瑾,等.电针镇痛后效应与脑干5-HT,下丘脑β-EP含量的关系[J].上海针灸杂志,2001,20(3):37-39.
    [45]陈瑾,刘光谱,周春阳.下丘脑β-EP及POMCmRNA的表达在针刺镇痛后效应中的作用[J].针刺研究,2004,29(1):5-9.
    [46]陈启盛,谢翠微,汤健,等.电针对大鼠不同脑区β-内啡呔含量的影响[J].科学通报,1983,(5):312-315.
    [47]詹睿,张露芬,严洁,等.针刺对佐剂性关节炎模型大鼠迟发期不同组织β-内啡肽影响的实验观察[J].中国中医基础医学杂志,2006,12(6):457-460.
    [48]孙红梅,胡波,郭长青,等.针刀松解法对第3腰椎横突综合征模型大鼠耐痛阈及脊髓与下丘脑ENK,β-EP的影响[J].北京中医药大学学报,2008,31(3):176-179.
    [49]韩济生.中枢阿片肽和胆囊收缩素功能活动的消长是决定针刺镇痛有效性的重要因素[J].北京医科大学学报,1996,28(5):321.
    [50]徐满英,杨春晓,石铁锋.脑内八肽缩胆囊素水平与提高针刺镇痛疗效的机制研究[J].中国临床康复,2003,7(31):4233-4235.
    [51]李振海.脑肠肽与针刺镇痛关系的研究进展[J].中医药导报,2008,14(5):113-115.
    [52]李丽,李洪安,蒋金芳,等.福尔马林致痛对大鼠脊髓背角神经元神经肽CCK表达的影响[J].中国应用生理学杂志,2009,25(2):217-220.
    [53]刘道强.针刺镇痛分子机制的研究进展[J].安徽中医学院学报,2002,21(3):60-62.
    [54]韩建中.针刺镇痛的分子生物学机理初探[J].江苏中医药,2002,23(3)27-28.
    [55]韩济生.中枢八肽胆囊收缩素的抗阿片作用是决定针刺镇痛和吗啡镇痛有效性的重要因素[J].生理科学进展,2000,31(2):173-177.
    [56]张丽娟.中枢八肽胆囊收缩素对抗阿片镇痛的分子机理研究[J].生理科学进展,1992,23(4):336-338.
    [57]刘苏星,沈上,于英心,等.坐骨神经切断大鼠脑脊液中CCK-8含量的动态变化及其与吗啡镇痛的关系.中国疼痛医学杂志,2004,10(6);352-356.
    [58]孙宇华,周岩,张志文,等.长时间电针时大鼠脑内八肤胆囊收缩素的生成和释放加速[J].神经科学,1995,2(2):83-88.
    [59]王学瑞,韩景献,宋学文,等.针刺“风府”穴对大鼠脑内神经肽胆囊收缩素基因表达的影响[J].中国针灸,1997,17(11):663.
    [60]孙锦平,尹岭,朱克.针刺的中枢调节机制研究进展[J].针刺研究,2003,28(2): 151-156.
    [61]杜小正,秦晓光,赵彬元,等.传统“热补”针法对实验性关节炎家兔的镇痛效应及脑脊液中β-EP,CCK-8含量的影响[J].针刺研究,2006,31(2)
    86-89.
    [62]Stanfa LC, Dickenson AH, Xu XJ, et al. Cholecystokinin and morphine analgesia:variations on a theme. Trends Pharmacol Sci,1994,15 (3):65.
    [63]Stanfa LC, Dickenson AH. Cholecystokinin as a factor in the enhanced potency of spinal morphine following carrageenin inflammation[J]. Br J Pharmacol, 1993,108 (4):967-975.
    [1]Murat N, Karadam B, Ozkal S, et al. Quantification of papain-induced rat Osteoarthritis in relation to time with the Mankin score[J]. Acta Orthop Traumatol Turc,2007,41 (3):233-237.
    [2]李忠仁.实验针灸学[M].北京:中国中医药出版社,2003,314.
    [3]胡元亮.实验动物针灸手册[M].北京:中国农业出版社,2003,288.
    [4]万选才,杨天祝,徐承焘,等.现代神经生物学[M].北京:北京医科大学中国协和医科大学联合出版社,1999,152-158.
    [5]张吉.针灸镇痛机制与临床[M].北京:人民卫生出版社,2002,168,239.
    [6]梁宜,方剑乔.5-羟色胺痛觉调制与针灸镇痛相关研究[J].上海针灸杂志,2009,28(8):492-495.
    [7]王胜,孙忠人,佟帅,等.针刺对实验性坐骨神经根压迫模型大鼠脑组织中单胺递质的影响[J].中国临床康复,2005,9(33):94-96.
    [8]梁繁荣,刘雨星,陈瑾.电针镇痛后效应与脑干5-HT,下丘脑p-EP含量的关系[J].上海针灸杂志,2001,20(3):37-39.
    [9]陈瑾,刘光谱,唐勇.中枢及外周5-HT,5-HIAA在针刺镇痛后效应中的作用[J].中医药学刊,2003,21(9):1446-1449.
    [10]梁繁荣,罗荣,刘雨星.电针镇痛后效应与炎症局部5-HT, NE, DA含量关系的实验研究[J].中国中医基础医学杂志,2001,7(11):52-55.
    [11]汪丛莹,樊小力.肾上腺素和五羟色胺在脊髓水平对痛传入信息的调节机制[J].西安医科大学学报,1995,16(2):222-224.
    [12]李辉,李云庆.5-羟色胺在脊髓影响伤害性信息传递的机能学和形态学基础[J].神经解剖学杂志,2002,18(3):265-268.
    [13]闫国平,李积胜.5-HT参与大鼠外侧网状核痛觉调制的可能机制[J].基础医学与临床,2003,23(5):568-569.
    [14]阮怀珍,李希成,蔡文琴.5-羟色胺和生长抑制素对P物质及慢痛引起的脊髓背角神经元电活动的影响[J].针刺研究,1996,21(3):27-31.
    [15]Bardin L, Lavarenne J, Eschalier A. Serotonin receptor subtypes involved in the spinal antinociceptive effect of 5-HT in rats[J]. Pain,2000,86(1-2):11-18.
    [16]Colpaert FC, Tarayre JP, Koek W, et al. Large-amplitude 5-HT1A receptor activation:a new mechanism of profound, central analgesia[J]. Neuropharmacology,2002,43 (6):945-958.
    [17]Deseure K, Koek W, Colpaert FC, et al. The 5-HT1A receptor agonist F 13640 attenuates mechanical allodynia in a rat model of trigeminal neuropathic pain[J]. Eur J Pharmacol,2002,456 (1-3):51-57.
    [18]Kukushkin ML, Igon'kina SI. Role of 5-HT3 receptors in the mechanisms of central pain syndrome[J]. Bull Exp Biol Med,2003,135 (6):552-555.
    [19]Xiao DQ, Zhu JX, Tang JS, et al.5-hydroxytryptamine 1A(5-HT1A)but not 5-HT3 receptor is involved in mediating the nucleus submedius 5-HT-evoked antinociception in the rat[J]. Brain Res,2005,1046(1-2):38-44.
    [20]Nishiyama T. Effects of a 5-HT2A receptor antagonist, sarpogrelate onthermal or inflammatory pain[J]. Eur J Pharmacol,2005,516 (1):18-22.
    [21]李晓泓,卢婧,孙红梅,等,针刀松解法对第3腰椎横突综合征大鼠痛阈及中枢单胺类神经递质影响的研究[J].北京中医药大学学报,2008,31(7):482-484,489.
    [22]Carol A, Warfield, Zahid H, Bajwa.疼痛医学原理与实践[M].北京:人民卫生出版社,2009,20.
    [23]Reddy SV, Maderdrut JL, Yaksh TL. Spinal cord pharmacology of adrenergic agonist-mediated antinociception[J]. J Pharmacol Exp Ther,1980,213(3):525-533.
    [24]Yaksh TL, Tyce GM. Microinjection of morphine into the periaqueductal gray evokes release of serotonin from spinal cord[J]. Brain Res,1979,171 (1):176-181.
    [25]Kuraishi Y, Harada Y, Satoh M, Takagi H. Akrtagonism by phenoxybenzamine of the analgesic effect of morphine injected into the nucleus reticularis gigantocellularis of the rat[J]. Neurapharmacology,1979,18(1):107-110.
    [26]董艺娜,明晓云,韩济生.中枢去甲肾上腺素和强啡肽A(1-17)在痛觉调制中的相互作用[J].中国疼痛医学杂志,1997,3(1);38-44.
    [27]Sparkes CG, Spencer PS. Antinociceptive activity of morphine after injection of biogenic amines in the cerebral ventricles of the conscious rat[J]. Br J Pharmacol, 1971,42 (2):230-241.
    [28]Mulphy DL, Lemer A, Rudniek G, et al. Serotonin transporter gene, genetic disorders, and pharmacogenetics[J]. Mol Interv,2004,4(2):109.
    [29]嵇波,刘清国,郭长青,等.针刀松解法,电针对膝骨关节炎兔中枢单胺类神经递质的影响[J].北京中医药大学学报,2009,32(9):598-602.
    [30]Stinus L, Cador M, Le MOA1M. Interaction between endogenous opioids and dopamine within the nucleus aeeumbens[J]. Ann N Y Acad Sci,1992,654: 254-273.
    [31]Liu QS, Qiao JT, Dafny N. LifeSci,1992,51 (19):1485-1492.
    [32]高秀,吴根诚.中枢多巴胺系统在痛觉调制中的作用研究[J].国外医学生理·病理科学与临床分册,2001,21(4):309-311.
    [33]王鲁娟,王亚南,孙嘉斌,等.蛛网膜下腔注射多巴胺对痛觉调制作用的研究[J].潍坊医学院学报,2007,29(2):114-116.
    [34]苏洁,张颖,于海.多巴胺对吗啡成瘾大鼠中枢痛觉的调制[J].中国临床康复,2006,10(14):102-104.
    [1]翁恩琪.痛与镇痛[M].上海:上海科学技术出版社,1987,181,235.
    [2]刘道强.针刺镇痛分子机制的研究进展[J].安徽中医学院学报,2002,21(3):60-62.
    [3]柯青,王廷华,赵有成.针刺镇痛及其机理[J].四川解剖学杂志,2002,10(4):225-230
    [4]张吉,张宁.针刺镇痛机制的探讨[J].中国针灸,2007,27(1):72-75.
    [5]赵志奇.疼痛及其脊髓机理[M].上海:上海科学教育出版社,2000,86.
    [6]朱长庚.神经解剖学[M].北京:人民卫生出版社,2002,451.
    [7]OttosonD, Physiology of the nervous system[J]. The macmillan press LTD London and Basingstoke,458-502.
    [8]阮怀珍,李希成,蔡文琴.5-羟色胺和生长抑制素对P物质及慢痛引起的脊髓背角神经元电活动的影响[J].针刺研究,1996,21(3):27-31.
    [9]高秀.针刺镇痛机制的研究[J].国外医学·中医中药分册,1999, (3)21-26.
    [l0]翁恩琪.痛与镇痛[M].上海:上海科学技术出版社,1987,231-232.
    [11]边景檀.脊髓中P物质参与电针镇痛的研究[J].生理科学进展,1995,26(4):325-328.
    [12]沈上,边景檀,田津斌,等.电针引起脊髓P物质释放的频率依赖性[J].生理学报,1996,48(1):89-93.
    [13]林亚平,彭艳,易受乡,等.不同电针频率刺激对胃扩张疼痛大鼠下丘脑内P物质,p-内啡呔表达的影响[J].针刺研究,2009,34(4):252-257.
    [14]赵斌,刘玉倩,王海涛,等.小针刀治疗肌肉损伤的组织学和生物力学研究[J].体育科学,2004,24(9):28-31.
    [15]郭长青,刘乃刚,李晓泓,等.针刀松解法对第三腰椎横突综合征大鼠血管活性物质的影响[J].针刺研究,2007,32(5):323-326.
    [16]乔晋琳,王健瑞,马广昊,等.针刀疗法对L3横突综合征兔血浆的影响[J].中国骨伤,2004,17(5):257-259.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700