左归丸对肾性骨病调控因子PTH、CT、CYP27B1的干预机制
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
目的探讨左归丸对5/6肾大部切除模型并ROD大鼠甲状旁腺、骨、肾脏多脏腑、多靶点的影响,研究左归丸防治ROD的作用机制,探讨补肾中药替代骨化三醇治疗SHPT的可行性及理论依据,为临床治疗CKD并发ROD的中药新药研究提供靶点依据。
     方法SPF级Wistar大鼠分为6组:正常对照组、假手术组、左归丸组、中药方组、骨化三醇组、模型组(每组n=8)。分别药物干预4周、8周、12周,检测血Cr、BUN、Hb、ALP、iPTH、Ca、P;药物干预12周麻醉处死大鼠,双能X线测量大鼠股骨骨密度(BMD),检测PTHmRNA、CTmRNA、CYP27B1mRNA表达,检测PTH、CT、CYP27B1蛋白水平,观察肾脏组织形态学改变。
     结果血Cr,药物干预4周时,正常对照组明显低于各组(P<0.01),模型组明显高于各组(P<0.01);药物干预8周时,除假手术组外,其余各组明显上升,且明显高于正常对照组(P<0.01),骨化三醇组、中药方组、假手术组明显低于模型组(P<0.01),中药方组明显低于左归丸组、骨化三醇组(P<0.01)(P<0.05);药物干预12周时,除假手术组外,各组明显高于正常对照组(P<0.01),中药方组明显低于模型组、骨化三醇组、左归丸组(P<0.01)(P<0.05)。
     血BUN,药物干预4周时,除假手术组外,正常对照组明显低于各组(P<0.01),中药方组、假手术组明显低于模型组(P<0.05)(P<0.01);药物干预8周时,正常对照组明显低于各组(P<0.01),中药方组明显低于左归丸组、骨化三醇组(P<0.05);药物干预12周时,各组明显高于正常对照组(P<0.01) (P<0.05),中药方组、骨化三醇组明显低于模型组(P<0.01) (P<0.05)。
     Hb,药物干预4周时,正常对照组明显高于各组(P<0.01),骨化三醇组、假手术组明显高于模型组(P<0.01);药物干预8周时,正常对照组明显高于各组(P<0.01) (P<0.05),中药方组明显高于左归丸组、骨化三醇组和模型组(P<0.01)(P<0.05)(P<0.01);药物干预12周时,各组明显低于正常对照组(P<0.01)(P<0.05),中药方组明显高于模型组(P<0.01)。
     血清ALP,在药物干预4周时,骨化三醇组明显低于正常对照组(P<0.05),左归丸组、骨化三醇组明显低于中药方组(P<0.01);药物干预8周时,模型组明显低于正常对照组(P<0.01)、高于假手术组(P<0.05);药物干预12周时,模型组明显高于正常对照组、骨化三醇组、假手术组(P<0.05) (P<0.01),左归丸组明显高于骨化三醇组(P<0.01)。
     iPTH,药物干预4周时,模型组、左归丸组明显高于正常对照组、假手术组(P<0.01) (P<0.05),中药方组、骨化三醇明显低于模型组(P<0.05),中药方组明显低于左归丸组(P<0.01);药物干预8周时,模型组明显高于中药方组、左归丸组、骨化三醇组(P<0.01);骨化三醇组明显高于左归丸组、中药方组(P<0.01)(P<0.05);药物干预12周时,正常对照组明显低于各组(P<0.01),模型组明显高于各组(P<0.01)。
     血清Ca,药物干预4周时,中药方组、假手术组和左归丸组明显高于模型组(P<0.01)和(P<0.05);药物干预8周时,模型组明显低于假手术组(P<0.01),左归丸组明显低于模型组、骨化三醇组(P<0.05)(P<0.01);药物干预12周时,模型组明显高于各组(P<0.01)(P<0.05)。
     血清P,药物干预4周时,模型组明显高于各组(P<0.01);药物干预8周时,模型组明显高于各组(P<0.01),左归丸、中药方组明显高于骨化三醇组(P<0.01)(P<0.05);药物干预12周时,模型组明显高于各组(P<0.01)(P<0.05),中药方组明显低于左归丸组(P<0.01)。
     BMD,模型组明显低于各组(P<0.01)(P<0.05),中药方组明显低于左归丸组、骨化三醇组(P<0.01)。
     PTHmRNA,正常对照组与假手术组、中药方组与模型组没有显著性差异(P>0.05),左归丸组明显低于骨化三醇组、中药组、模型组(P<0.01),骨化三醇组明显低于中药组、模型组(P<0.01)。
     CTmRNA正常对照组与假手术组、模型组没有显著性差异(P>0.05),左归丸组明显高于各组(P<0.01),中药组明显高于除左归丸以外的各组(P<0.01),骨化三醇组明显低于模型组(P<0.01)。
     PTH,各组蛋白表达明显高于正常对照组(P<0.01);中药方组明显低于模型组、左归丸组、骨化三醇组(P<0.01);左归丸组明显低于模型组、骨化三醇组(P<0.05)。
     CT,正常对照组的表达明显高于各组(P<0.01);模型组明显低于中药方组、骨化三醇组及左归丸组(P<0.01);左归丸组明显低于中药方组、骨化三醇组(P<0.01)。蛋白质
     甲状旁腺PCNA,在正常对照组中表达最弱,在模型组中表达最强,且两组有显著性差异(P<0.01);骨化三醇组比中药方组表达弱(P<0.01),左归丸组比中药方组、骨化三醇组表达弱(P<0.01) (P<0.05)。
     CYP27B1mRNA,假手术组明显高于各组(P<0.01),模型组明显低于各组(P<0.01),左归丸组明显低于中药方组、骨化三醇组、模型组(P<0.01),中药方组与骨化三醇组没有显著性差异(P>0.05)。
     CYP27B1蛋白表达,模型组明显低于各组(P<0.01),左归丸明显低于中药方组、骨化三醇组(P<0.01),中药方组与骨化三醇组没有差异(P>0.05)。
     CYP27B1免疫荧光结果:正常对照组、假手术组表达强;模型组比各组表达弱(P<0.05);中药方组较左归丸组、骨化三醇组表达强(P<0.01);左归丸组比骨化三醇组表达弱(P<0.05)。
     结论5/6肾大部切除大鼠模型造模成功并发ROD表现。ROD药物的干预应从肾功不良初期进行,建立预防模式。左归丸能改善ROD的骨营养不良,对PTH有直接的抑制作用,其机制可能是通过调节钙磷代谢及参与成骨细胞代谢的途径。左归丸对甲状旁腺、甲状腺、骨有多重作用,可抑制甲状旁腺的增生,抑制破骨细胞活性,其对ALP的调节作用将预示在改善骨营养不良方面将比骨化三醇更有优势。
     左归丸和骨化三醇不能有效地控制Cr的升高以及Hb的降低,他们不能有效改善肾功能不良、纠正贫血。在血Cr、BUN、Hb水平控制方面,中药方组显示出的明显优势提示其可能与左归丸有互补效应。中药方干预能保护肾脏,左归丸与中药方合用可能在抑制SHPT、改善钙磷代谢、调动成骨系统、纠正贫血、延缓肾脏病的进展方面的效果会优于骨化三醇,两方可能有互补和协同效应。
     基于左归丸对其靶器官甲状旁腺、甲状腺、骨的影响,可能会成为临床替代骨化三醇对ROD进行早期干预的经方,佐以补肾生精益气活血中药,对慢性肾脏病进展的控制可能会有极大帮助。
Objective To Discussion the influence of Zuoguiwan on the parathyroid, bone, and kidney of rat model with renal osteodystrophy (ROD) created by 5/6 renal resection. Moreover,the mechanisms were also investigated in order to provide more target proof in treating CKD complicating ROD by herbs of invigorating Shen.
     Methods Wistar rats of SPF grade were divided into six groups:normal control group, sham operation group, Zuoguiwan group, herbal group, Calcitriol group and model group (each n=8). Respective drug was administrated for 4 weeks,8 weeks,12 weeks in each group. Thereafter, the blood Cr, BUN, Hb,ALP, iPTH, Ca, P were tested;The rats were anesthetized and killed after drug 12-week intervention.The femur bone mineral density (BMD) was measured by dual energy X-ray. The expressions of PTHmRNA,CTmRNA,CYP27B1mRNA were detected by Real-time PCR and the protein levels of PTH,CT,CYP27B1 were also determined by western blotting. In addition,the morphologic changes of kidney was observed.
     Results Serum Cr levels of normal control group was significantly lower than other groups after 4-week intervention(P<0.01). In the model group,the levels of Cr was higher than that of other groups (P<0.01). Eight weeks after intervention,the serum Cr levels of other groups had significantly increased except to sham group,the Cr level of the other group was significantly higher than the control group (P<0.01). In the Calcitriol groud,herbal group and sham operation,the levels of serum Cr were significantly lower than that of the model group (P<0.01).Indeed,level of Cr the herbal group much significantly lower when compared with the Zuoguiwan group and Calcitriol group(P<0.01 or P<0.05).Excepting to the sham group,the Cr level of the other groups were significantly higher than normal control group 12 weeks after drug intervention (P<0.01).In the herbal group,the Cr level of was significantly lower than that of the model group,Calcitriol group and Zuoguiwan group(P<0.01 or P<0.05).
     Serum BUN levels of the normal group was significantly lower than other group after 4-week intervention excepting to the sham group(P <0.01).In herbal group and sham operation group,the levels of BUN were significantly lower than that of model group(P<0.05 or P<0.01).Eight weeks after intervention,the BUN level of normal control group was significantly lower than other group (P<0.01).In the herbal group,the level of BUN was significantly lower than that of Zuoguiwan group and calcitriol group(P<0.05).The BUN level of the other group was significantly higher than the control group 12 weeks after drug intervention(P<0.01 or P<0.05).In the herbal group and Calcitriol group,the BUN level of were significantly lower than that of model group(P<0.01 or P<0.05).
     Serum Hb levels of the normal control group was significantly higher than other group after 4-week intervention(P<0.01).In the Calcitriol group and shan operation group,the level of Hb were higher than that of model group(P<0.01).Eight weeks after intervention,the Hb level of normal control group was significantly higher than other group(P<0.01 or P<0.05).In the herbal group,the level of Hb was significantly higher than that of Zuoguiwan group,Calcitriol group and model group(P<0.01orP<0.05or P<0.01).The Hb level of the other group was significantly lower than that of the control group 12 weeks after drug intervention(P<0.01 or <0.05). The Hb level of herbal group was significantly higher than that of model group (P<0.01).
     Serum ALP level in Calcitriol group was significantly lower than that in normal control group (P<0.05) after 4-week intervention. The ALP levels in Zuoguiwan group and Calcitriol group were markedly lower than that in herbal group (P<0.01).Eight weeks after intervention, the ALP level of model group was significantly lower than that of the control group (P<0.01) and was significantly higher sham operation group(P<0.05).The ALP level of the model group was significantly higher than that of the control group, Calcitriol group and sham operation group respectively 12 weeks after drug intervention(P<0.05 or P<0.01). The ALP level of Zuoguiwan group was significantly higher than that of Calcitriol group (P<0.01).
     Serum iPTH levels of model group and Zuoguiwan group were significantly higher than those of normal control group and sham operation group after 4-week intervention(P<0.01 or P<0.05). In the herbal group and Calcitriol group,the levels of iPTH were lower than that of the model group (P<0.05). Compared with the Zuoguiwan group,the herbal group had significantly lower level of iPTH(P<0.01).Eight weeks after intervention,the iPTH level of the model group was significantly higher than that of herbal group,Zuoguiwan group and Calcitriol group(P<0.01). In addition,Zuoguiwan group and herbal group had lower levels of iPTH than Calcitriol group (P <0.05 or P<0.01).12 weeks after drug intervention,the iPTH level of the normal control group was significantly lower than other groups (P<0.01),the iPTH level of model group was significantly higher than other groups (P <0.01).
     Serum Ca levels of herbal group,sham operation group and Zuoguiwan group were significantly higher than model group 4 weeks after drug intervention (P<0.01 or P<0.05).Eight weeks after intervention,the Serum Ca level of the model group was significantly lower than sham operation group (P <0.01),In the Zuoguiwan group,the levels of Ca were lower than that of the model group and Calcitriol group (P<0.05 or P<0.01).Serum Ca levels of the model group was significantly higher than other groups 12 weeks after drug intervention (P<0.01 or P<0.05).
     Serum P levels of model group was significantly higher than other groups after 4-week intervention(P<0.01). Eight weeks after intervention,the Serum P level of model group was significantly higher than other groups(P<0.01),In the Zuoguiwan group and herbal group,the Serum P level of were higher than that of calcitriol group(P<0.01 or P<0.05). The P level of the model group was significantly higher than other groups 12 weeks after drug intervention(P<0.01 or<0.05). The P level of herbal group was significantly lower than Zuoguiwan group(P<0.01).
     The BMD of the model group was significantly lower than other groups(P<0.01 or P<0.05).In the herbal group,the BMD was significantly lower than that of Zuoguiwan group and Calcitiol group (P<0 .01).
     PTHmRNA levels of betweening control group and sham operation group,herbal group and model group had not significant difference(P>0.05).In the Zuoguiwan group,the PTHmRNA level of was significantly lower than that of Calcitriol group,herbal group and model group(P<0.01). Indeed,level of PTHmRNA the Calcitriol group much significantly lower when compared with the herbal group and model group(P<0.01).
     CTmRNA levels of betweening control group and sham operation group,herbal group and model group had not significant difference(P > 0.05).In the Zuoguiwan group,the CTmRNA level of was significantly higher than that of other group(P<0.01). Excepting to Zuoguiwan group,compared with the herbal group,other group had significantly higher level of CTmRNA(P<0.01). CTmRNA levels of Calcitriol group was significantly lower than that of model group(P<0.01).
     The PTH protein expression of the other group was significantly higher than that of the control group(P<0.01).In the herbal group,the PTH of was significantly lower than that of model group,Zuoguiwan group and Calcitriol group(P<0.01). In addition,Zuoguiwan group and model group,Calcitriol group had lower protein expression of PTH(P<0.05).
     The CT protein expression of the control group was significantly higher than that of the other group(P<0.01).In the model group,the CT of was significantly lower than that of herbal group,Calcitriol group and Zuoguiwan group(P<0.01).In addition,Zuoguiwan group and herbal group,Calcitriol group had lower protein expression of CT(P<0.01).
     The PCNA expression of the normal control group was the weakest, in the model group,was the strongest expression and had significantly differ(P<0.01).Compared with the Calcitriol group,the herbal group had significantly weaker expression of PCNA(P<0.01).In the Zuoguiwan group, the expression of PCNA was weaker than that of the herbal group and Calcitriol group(P<0.01 or P<0.05).
     CYP27B1mRNA levels of sham operation group was significantly higher than the other group(P<0.01). CYP27B1mRNA levels of the model group was significantly lower than that of other group(P<0.01).In the Zuoguiwan group,the CYP27B1mRNA level of was significantly lower than that of herbal group,Calcitriol group and model group(P<0.01). Compared with the herbal group,Calcitriol group had not significantly differ level of CYP27B1mRNA (P> 0.05).
     The CYP27B1 protein expression of the model group was significantly lower than the other group(P<0.01).In Zuoguiwan group,the CYP27B1 of was significantly lower than that of herbal group, Calcitriol group(P<0.01). Compared with the herbal group,Calcitriol group had not significantly differ the protein expression of CYP27B1 (P> 0.05).
     In the normal control group and sham operation group,the protein fluorescence expression of CYP27B1 were the strongest. Compared with the' model group,the other group had significantly weaker fluorescence expression of CYP27B1(P< 0.05).CYP27B1 immunofluorescence expression of herbal group was significantly stronger than that of Zuoguiwan group and Calcitriol group(P< 0.01).Compared with the Zuoguiwan group,calcitriol group had signifiticantly weaker the protein fluorescence expression of CYP27B1(P< 0.05).
     Conclusion ROD rat model of 5/6 renal resection are successfully created.Treatment or prevention with traditional Chinese herb or Zuoguiwan should began from incipience of renal dysfunction.Zuoguiwan can improve renal osteodystrophy bone malnutrition, and has a direct inhibitory effect on parathyroid hormone,which might be contributed to the regulation of calcium,phosphorus and bone cell metabolism.Zuoguiwan may play a role on glandulae parathyroideae, glandula thyreoideaand bone may inhibit parathyroid hyperplasy and osteoclast cytoactive.The regulation on the ALP suggest that Zuoguiwan is better than Calcitriol in improving osteodystrophy.
     Zuoguiwan and Calcitriol can not effectively control the Cr,increase Hb, improve renal dysfunction and anemia. However,serum Cr,BUN,Hb level could be improved by the treatment in the herbal group which suggested that they are complementory. TCM treatmen can protect kidney function.The two groups combined with each other may be better than Calcitriol treatment in inhibiting secondary hyperparathyroidism,regulating calcium and phosphorus metabolism,mobilizing bone formation system,correcting anaemia and defering renal disease. Two treatments can be complementory and synergistic.
     Base on the effect of Zuoguiwan on target organ glandula thyreoidea, glandulae parathyroideae and bone,Zuoguiwan should became a classical prescriptions that ROD is treated early to instead of Calcitriol in clinic,adding to herbs of invigorating Shen to generate marrow and supplementing qi and activating blood circulation,they could had actively help for control of disease advancement of chronicity renal.
引文
[1]Dunstan CR, Hills E, Norman AW, et al. Treatment of hemodialysis bone disease with 24,25(OH)2D3 and 1,25(OH)2D3 alione of in combination[J]. Min Electrol Metab,1985; 11:358.
    [2]Poulsom R, Forbes SJ, Hodivala-Dilke K, et al. Bone marrow contributes to renal parenchymal turnover and regeneration[J]. J Pathol, 2001; 195:229-235.
    [3]Imasawa T, Utsunomiya, Kawamura T, et al. The potential of bone marrow-derived cells to differentiate to glomerular mesangial cells[J]. J Am Soc Nephrol,2001; 12:1401-1409.
    [4]Oliver JA. Adult renal stem cells and renal repair [J]. Curr Opin Nephrol Hypertens,2004; 13(1):17-22.
    [5]Caldas HC, Fernandes IM, Gerbi F, et al. Effect of whole bone marrow cell infusion in the progression of experimental chronic renal failure[J]. Transplant Proc,2008; 40(3):853-5.
    [6]Jiang Y, Jahagirdar BN, Reinhardt RL, et al. Pluripotency of mesenchymal stem cells derived from adult marrow[J]. Nature,2002; 418(6893):41-49.
    [7]Sung HJ, Hong SC, Yoo JH, et al. Human MSCs that are neurally modified with this methodology could be a useful source of cells for CNS repair and regeneration[J]. J Korean Med Sci,2010; 25(10): 1418-26.
    [8]周家俊,关鑫,赵东.部分肾切除加高磷饮食所致大鼠肾性骨病模型研究[J].中国中西医结合肾病杂志,2002;3(10):567-569.
    [9]James B Wetmore, L Darryl Quarles.Calcimimetics or vitamin D analogs for suppressing parathyroid hormone in end-stage renal disease:time for a paradigm shift? [J]. Nature Clinical Practice Nephrology,2009; 5(1):24-33.
    [10]Pena YT, Soyibo AK, McGrowder D, et al. The importance of bone biomarkers in the diagnosis of renal osteodystrophy [J]. West Indian Med J,2010; 59(3):332-7.
    [11]Toussaint ND, Elder GJ, Kerr PG. Bisphosphonates in chronic kidney disease; balancing potential benefits and adverse effects on bone and soft tissue[J]. Clin J Am Soc Nephrol,2009; 4(1): 221-33.
    [12]Okuno S, Inaba M. Biochemical markers of bone turnover. New aspect. Dialysis and bone metabolic marker[J]. Clin Calcium, 2009; 19(8):1084-91.
    [13]Toshimasa Shinki, Yutaka ueno, Hector F, et al.Calcitonin is a maj or regulator for the expression of renal 25-hydroxyvitamin D3-1 a-hydroxylase gene in normocalcemic rats[J]. Physiology,1999; 96: 8253-8258.
    [14]Helvig CF, Cuerrier D, Hosfield CM, et al. Dysregulation of renal vitamin D metabolism in the uremic rat[J]. Kidney Int,2010; 78(5):463-72.
    [15]Geng S, Zhou S, Glowacki J. Effects of 25-hydroxyvitamin D(3) on proliferation and osteoblast differentiation of human marrow stromal cells require CYP27B1/1 α-hydroxylase[J]. J Bone Miner Res,2011; 26(5):1145-53.
    [16]李恩主编.中国肾藏象理论传承与现代研究[M],北京:人民卫生出版社,2007,第一版:160.
    [17]陈主初主编.病理生理学[M],北京:人民卫生出版社,2006,第一版:91.
    [18]李恩主编.中国肾藏象理论传承与现代研究[M],北京:人民卫生 出版社,2007,第一版:159.
    [19]Fedde K. Human osteosarcoma cells spontaneously release matrix-vessi-cle-like structures with the capacity to mineralize[J]. Bone Miner,1992; 17(2):145.
    [20]Dziedziejko V, Safranow K, Slowik-Zylka D, et al. Comparison of rat and human alkaline phosphatase isoenzymes and isoforms using HPLC and electrophoresis[J]. Biochim Biophys Acta,2005; 1752(1):26.
    [21]Urena P, Prieur P, Petrover M. Alkaline phosphatase of bone origin in hemodialyzed patients[J]. Presse Med,1996; 25(29):1320.
    [22]Hashidate H, Kamimura M, Nakagawa H, et al. Early changes in bone specific turnover markers during the healing process after vertebral fracture [J]. Open Orthop J,2011; 14(5):32-6.
    [23]Urena P, Prieur P, Petrover M. Calcitriol may directly suppress bone turnover[J]. Nephron,1997; 75(1):116.
    [24]Baskin E, Besbas N, Saatci U, et al. Biochemical markers of bone turnover in the diagnosis of renal osteodystrophy in dialyzed children[J]. Turk J Pediatr,2004; 46(1):28.
    [25]孙琳林,康广盛,韩海荣,等.左归丸实验研·究概况[J].中成药,201 0;32(3):477-480.
    [26]李恩主编.中国肾藏象理论传承与现代研究[M],北京:人民卫生出版社,2007,第一版:119.
    [27]刘 平主编.现代中医肝脏病学[M],北京:人民卫生出版社,2001,第一版:23.
    [28]刘国君,张爱平,李宝玲.左归丸对小鼠阿尔茨海默症模型的保护作用[J].临床合理用药,2010;18(3):91-92.
    [29]刘梅洁,吕国红,邹 军,等.左归丸含药血清对成骨细胞分泌骨钙素的影响[J].中国中医基础医学杂志,2007;8(13):581-582.
    [30]李勇,等.淫羊藿黄酮对体外培养成骨细胞的影响[J].中国药科大 学学报,2002;33(1):48.
    [31]马慧萍,贾正平,等.淫羊藿总黄酮含药血清促进骨髓间充质干细胞增殖和成骨分化[J].中国骨质疏松杂志,2004;10(4):420-422.
    [32]许春姣,郭峰,高清平,等.骨髓基质干细胞与黄芪-壳聚糖/聚乳酸支架对犬牙周骨缺损再生的影响[J].中南大学学报(医学版),2006;31(4):312-317.
    [33]薛艳芸,张立新.黄芪、灯盏花素对实验性糖尿病大鼠肾脏内皮素-1、TGF-β1的作用[J].细胞与分子免疫学杂志,2010;26(9):935-945.
    [34]Naya M, Tsukamoto T, Inubushi M, et al. Elevated plasma plasmino-gen activator inhibitor type-1 is a independent predictor of coronary mi-crovascular dysfunction in hypertension[J]. Circ J,2007; 71(3):348-533.
    [35]Dupont D M, Madsen J B, Kristensen T, et al. Biochemical properties of plasminogen activator inhibitor-1[J]. Front Biosci, 2009; 14:1337-1361.
    [36]杨长春,马增春.黄芪、当归对血管内皮细胞纤溶酶原激活物抑制剂-1的影响[J].第三军医大学学报,2010;32(11):1149-1151.
    [37]姚文兵,陈琼华.大黄的生化学研究ⅩⅩx111波叶大黄多糖的降血脂和抗凝血作用[J].中国药科大学学,1990;21(5):283-286.
    [38]姚文兵,陈琼华.大黄的生化学研究ⅩⅩx111波叶大黄多糖对免疫功能的促进作用[J].中国药科大学报,1990;21(2):99-102.
    [39]朱深银,周远大,杜冠华.大黄和泽泻提取物对二甘醇致小鼠肾脏损伤的保护作用研究[J].中药研究,2009;20(9):641-643.
    [40]陈琼花,郑武飞,苏学良,等.中药大黄的综合研究[J].药学学报,1962;9(12):757-762.
    [41]Chang E J, Lee W J, Cho SH, etal. Proliferative effects of Flavan-3-ols and propelargonidins from rhizomes of Drynariafortunei on MCF-7 and osteoblasticcells[J]. Arch Pharms,2003; 26(8):620.
    [42]樊粤光,黄永明,曾意荣,等.骨碎补提取液对体外分离破骨细胞性骨吸收的作用[J].中国中医骨伤科杂志,2003;11(6):4-6.
    [1]Dunstan CR, Hills E, Norman AW, et al. Treatment of hemodialysis bone disease with 24,25(OH)2D3 and 1,25(OH)2D3 alione of in combination[J]. Min Electrol Metab,1985; 11:358.
    [2]李 恩主编.中国肾藏象理论传承与现代研究[M],北京:人民卫生出版社,2007,第一版:119.
    [3]刘 平主编.现代中医肝脏病学[M],北京:人民卫生出版社,2001,第一版:23.
    [4]徐孝云,刘宝云.益肾壮骨汤治疗慢性肾小球肾炎肾虚证骨密度改善的临床研究[J].北京中医,1996;15(5):62.
    [5]张 宁,张宇忠,齐尔家,等.补肾活血法改善肾衰大鼠骨代谢异常的实验研究[J].中国医药学报,2000;15(6):68--70.
    [6]关 鑫,周家俊,赵 东.补肾壮骨汤干预治疗肾性骨病大鼠模型的实验研究[J].中国中西医结合肾病杂志,2003;4(1):10-12.
    [7]朱鹏飞,李冬华.肾主骨理论的现代理解与补肾法的研究[J].上海中医药杂志,2003;37(6):9.
    [8]安海燕,任 可.补骨汤治疗肾性骨病的临床观察[J].中国中西医结合肾病杂志,2004;5(12):718-719.
    [9]张 宁,刘世巍,任 可,等.补肾活血法对肾性骨病患者全段甲状旁腺素与骨特异性碱性磷酸酶的影响[J].北京中医药大学学报,2005;12(4):1-3.
    [10]张 宁,刘世巍,任 可,等.补肾活血法对肾性骨病患者全段甲状旁腺素与骨特异性碱性磷酸酶的影响[J].北京中医药大学学报(中医临床版),2005;12(4):1-3.
    [11]李 良,刘南梅.补肾健骨汤治疗肾性骨病疗效观察[J].中国中医急症,2008;17(8):1068-1069.
    [12]李 勇.淫羊藿黄酮对体外培养成骨细胞的影响[J].中国药科大学 学报,2002;33(1):48.
    [13]马慧萍,贾正平.淫羊藿总黄酮含药血清促进骨髓间充质干细胞增殖和成骨分化[J].中国骨质疏松杂志,2004;10(4):420-422.
    [14]许春姣,郭 峰,高清平,等.骨髓基质干细胞与黄芪-壳聚糖/聚乳酸支架对犬牙周骨缺损再生的影响[J].中南大学学报(医学版),2006;31(4):312-317.
    [15]王小琴,邵朝弟,谭大琦,等.肾安颗粒治疗慢性肾衰竭的临床研究[J].中国中西医结合肾病杂志,2003;4(7):393-395.
    [16]王小琴,谭大琦,李卫星,等.复方黄芪甲苷、淫羊霍苷、大黄蒽醌提取物对残余肾模型PCNA表达及肾功能的影响[J].临床医药杂志,2005;18(2):1-13.
    [17]王小琴,邵朝弟,金劲松,等.肾安提取液对5/6肾切除模型肾组织学的影响[J].临床肾脏病杂志,2004;4(2):76-79.
    [18]王小琴,邵朝弟,金劲松,等.肾安提取液对5/6肾切除大鼠肾功能的影响[J].临床肾脏病杂志,2006;6(4):179-181.
    [19]王小琴,邵朝弟,金劲松. 肾安提取液对大鼠残余肾的病理学影响[J].中国中西医结合肾病杂,2007;8(12):716-717,I0009.
    [20]卢祖礼,徐大龙,王小琴,等.肾安Ⅰ号对大鼠GMC增殖及TGF—β1、HGF表达的影响[J].中国中西医结合肾病杂志,2006;7(12): 721-723.
    [21]何太文,王小琴,张利.肾安Ⅱ号对体外培养大鼠GMC增殖及NF—κB表达的影响[J].河南中医,2009;29(2):136-138.
    [22]王小琴.肾安提取液对3T3细胞增殖α-肌动蛋白表达影响的实验研究[J].中医药导报,2006;12(10):10-12.
    [23]翟建梅.肾性骨病的防治进展[J].中外医疗,2008;25:142-143.
    [24]赵 丽.肾性骨病治疗研究进展[J].河北医药,2009;31(13):1642-1644.
    [25]Pittenger MF, Mackay AM, Jaiswal SC, et al. Multilineage potential of adult human mesenchymal stem cells[J]. Science,1999; 284(5411): 143-147.
    [26]Makino S, Fukuda K, Miyoshi s, et al. Cardiomyocytes can be generated from marrow stromal cells in vitro[J]. J Clin Invest,1999; 103(5):697-705.
    [27]Woodbury D, Schwarz EJ, Prockop DJ, et al. Adult rat and human bone marrow stromal cells differentiate into neurons [J]. J Neursci Res, 2000; 61(4):364-370.
    [28]孙晓春,许文荣.胎儿骨髓间质干细胞体外诱导为神经细胞的初步实验研究[J].中国生物医学工程学报,2003;23(1):40-43.
    [29]Poulsom R, Forbes SJ, Hodivala-Dilke K, et al. Bone marrow contributes to renal parenchymal turnover and regeneration[J]. J Pathol, 2001; 195:229-235.
    [30]Imasawa T, Utsunomiya, Kawamura T, et al. The potential of bone marrow-derived cells to differentiate to glornerular mesangial cells[J]. J Am Soc Nephrol,2001; 12:1401-1409.
    [31]Jiang Y, Jahagirdar BN, Reinhardt RL, et al. Pluripotency of mesenchymal stem cells derived from adult marrow[J]. Nature,2002; 418(6893); 41-49.
    [32]孙晓春,许文荣,朱 伟,等。大鼠骨髓间质干细胞体外分化为成骨细胞的实验研究[J].江苏大学学报(医学版),2004;14(5):369-370,374.
    [33]陈主初主编.病理生理学[M],北京:人民卫生出版社,2008,第一版:90-91.
    [34]金慰芳,于志锋,高建军,等.PTH对骨髓细胞骨代谢相关基因表达的影响[J].中国骨质疏松杂志,2005;11(3):286-288.
    [35]李恩主编.中国肾藏象理论传承与现代研究[M],北京:人民卫生出版社,2007;第一版:159.
    [36]Fedde K. Human osteosarcoma cells spontaneously release matrix-vessi-cle-like structures with the capacity to mineralize[J]. Bone Miner,1992; 17(2):145.
    [37]Dziedziejko V, Safranow K, Slowik-Zylka D, et al. Comparison of rat and human alkaline phosphatase isoenzymes and isoforms using HPLC and electrophoresis[J]. Biochim Biophys Acta,2005; 1752(1): 26.
    [38]Urena P, Prieur P, Petrover M, et al. Alkaline phosphatase of bone origin in hemodialyzed patients[J]. Presse Med,1996; 25(29):1320.
    [39]Urena P, Hruby M, Ferreira A, et al. Plasma total versus bone alkaline phosphatase as markers of bone turnover in hemodialysis patients[J]. Jam Soc Nephrol,1996; 7(3):506.
    [40]Urena P, Prieur P, Petrover M, et al. Calcitriol may directly suppress bone turnover[J]. Nephron,1997; 75(1):116.
    [41]Baskin E, Besbas N, Saatci U, et al. Biochemical markers of bone turnover in the diagnosis of renal osteodystrophy in dialyzed children[J]. Turk J Pediatr,2004; 46(1):28.

© 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