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Evidence-Based Complementary and Alternative Medicine
Volume 2011 (2011), Article ID 109809, 8 pages
http://dx.doi.org/10.1093/ecam/nep115
Original Article

Paeoniae alba Radix Promotes Peripheral Nerve Regeneration

1Graduate Institute of Chinese Medical Science, China Medical University, Taiwan
2Division of Neurosurgery, China Medical University Hospital, Taiwan
3Department of Health and Nutrition Biotechnology, Asia University, Taiwan
4Department Biomedical Imaging and Radiological Science, China Medical University, Taichung, Taiwan

Received 25 March 2009; Accepted 21 July 2009

Copyright © 2011 Kun-Shan Huang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. E. G. Fine, I. Decosterd, M. Papaloïzos, A. D. Zurn, and P. Aebischer, “GDNF and NGF released by synthetic guidance channels support sciatic nerve regeneration across a long gap,” European Journal of Neuroscience, vol. 15, no. 4, pp. 589–601, 2002. View at Publisher · View at Google Scholar · View at Scopus
  2. J. G. Boyd and T. Gordon, “A dose-dependent facilitation and inhibition of peripheral nerve regeneration by brain-derived neurotrophic factor,” European Journal of Neuroscience, vol. 15, no. 4, pp. 613–626, 2002. View at Publisher · View at Google Scholar · View at Scopus
  3. S. Yoshii, M. Oka, M. Shima, A. Taniguchi, and M. Akagi, “30 mm regeneration of rat sciatic nerve along collagen filaments,” Brain Research, vol. 949, no. 1-2, pp. 202–208, 2002. View at Publisher · View at Google Scholar · View at Scopus
  4. E. Verdú, R. O. Labrador, F. J. Rodríguez, D. Ceballos, J. Forés, and X. Navarro, “Alignment of collagen and laminin-containing gels improve nerve regeneration within silicone tubes,” Restorative Neurology and Neuroscience, vol. 20, no. 5, pp. 169–179, 2002. View at Google Scholar · View at Scopus
  5. P. Liu, L. Zhao, S.-L. Zhang, and J.-Z. Xiang, “Modified Wendan decoction can attenuate neurotoxic action associated with Alzheimer's disease,” Evidence-Based Complementary and Alternative Medicine, vol. 6, no. 3, pp. 325–330, 2009. View at Publisher · View at Google Scholar · View at Scopus
  6. K. G. Mohandas Rao, S. Muddanna Rao, and S. Gurumadhva Rao, “Centella asiatica (L.) leaf extract treatment during the growth spurt period enhances hippocampal CA3 neuronal dendritic arborization in rats,” Evidence-Based Complementary and Alternative Medicine, vol. 3, no. 3, pp. 349–357, 2006. View at Publisher · View at Google Scholar · View at Scopus
  7. Y.-S. Chen, C.-J. Liu, C.-Y. Cheng, and C.-H. Yao, “Effect of bilobalide on peripheral nerve regeneration,” Biomaterials, vol. 25, no. 3, pp. 509–514, 2004. View at Publisher · View at Google Scholar · View at Scopus
  8. Y.-S. Chen, C.-H. Wu, C.-H. Yao, and C.-T. Chen, “Ginsenoside Rb1 enhances peripheral nerve regeneration across wide gaps in silicone rubber chambers,” International Journal of Artificial Organs, vol. 25, no. 11, pp. 1103–1108, 2002. View at Google Scholar · View at Scopus
  9. D.-Z. Liu, K.-Q. Xie, X.-Q. Ji, Y. Ye, C.-L. Jiang, and X.-Z. Zhu, “Neuroprotective effect of paeoniflorin on cerebral ischemic rat by activating adenosine A1 receptor in a manner different from its classical agonists,” British Journal of Pharmacology, vol. 146, no. 4, pp. 604–611, 2005. View at Publisher · View at Google Scholar · View at Scopus
  10. C. Y. Wu, Outline of New China Herbals, Shanghai Science and Technology Press, Shanghai, China, 1990.
  11. S.-H. Wu, S.-M. Yang, D.-G. Wu, Y.-W. Cheng, and Q. Peng, “Three novel 24,30-dinortriterpenoids, paeonenoides A-C, from Paeonia veitchii,” Helvetica Chimica Acta, vol. 88, no. 2, pp. 259–265, 2005. View at Publisher · View at Google Scholar · View at Scopus
  12. L. A. Greene and A. S. Tischler, “Establishment of a noradrenergic clonal line of rat adrenal pheochromocytoma cells which respond to nerve growth factor,” Proceedings of the National Academy of Sciences of the United States of America, vol. 73, no. 7, pp. 2424–2428, 1976. View at Google Scholar · View at Scopus
  13. P. Hu, Q.-L. Liang, G.-A. Luo, Z.-Z. Zhao, and Z.-H. Jiang, “Multi-component HPLC fingerprinting of Radix Salviae Miltiorrhizae and its LC-MS-MS identification,” Chemical and Pharmaceutical Bulletin, vol. 53, no. 6, pp. 677–683, 2005. View at Publisher · View at Google Scholar · View at Scopus
  14. S. F. Swaim, “Peripheral nerve surgery,” in Veterinary Neurology, J. E. Oliver, B. F. Hoerlein, and I. G. Mayhew, Eds., pp. 493–512, WB Saunders, Pennsylvania, Pa, USA, 1987. View at Google Scholar
  15. V. I. Shubayev and R. R. Myers, “Matrix metalloproteinase-9 promotes nerve growth factor-induced neurite elongation but not new sprout formation in vitro,” Journal of Neuroscience Research, vol. 77, no. 2, pp. 229–239, 2004. View at Publisher · View at Google Scholar · View at Scopus
  16. C. Romano, R. A. Nichols, P. Greengard, and L. A. Greene, “Synapsin I in PC12 cells. I. Characterization of the phosphoprotein and effect of chronic NGF treatment,” Journal of Neuroscience, vol. 7, no. 5, pp. 1294–1299, 1987. View at Google Scholar · View at Scopus
  17. C. Romano, R. A. Nichols, and P. Greengard, “Synapsin I in PC12 cells. II. Evidence for regulation by NGF of phosphorylation at a novel site,” Journal of Neuroscience, vol. 7, no. 5, pp. 1300–1306, 1987. View at Google Scholar · View at Scopus
  18. G. Lundborg, B. Rosen, S. O. Abrahamson, L. Dahlin, and N. Danielsen, “Tubular repair of the median nerve in the human forearm: preliminary findings,” Journal of Hand Surgery, vol. 19, no. 3, pp. 273–276, 1994. View at Publisher · View at Google Scholar · View at Scopus
  19. J. B. Johnston, C. Silva, J. Holden, K. G. Warren, A. W. Clark, and C. Power, “Monocyte activation and differentiation augment human endogenous retrovirus expression: implications for inflammatory brain diseases,” Annals of Neurology, vol. 50, no. 4, pp. 434–442, 2001. View at Publisher · View at Google Scholar · View at Scopus
  20. S. Tsutsui, J. Schnermann, F. Noorbakhsh et al., “A1 adenosine receptor upregulation and activation attenuates neuroinflammation and demyelination in a model of multiple sclerosis,” Journal of Neuroscience, vol. 24, no. 6, pp. 1521–1529, 2004. View at Publisher · View at Google Scholar · View at Scopus
  21. H.-Q. Liu, W.-Y. Zhang, X.-T. Luo, Y. Ye, and X.-Z. Zhu, “Paeoniflorin attenuates neuroinflammation and dopaminergic neurodegeneration in the MPTP model of Parkinson's disease by activation of adenosine A1 receptor,” British Journal of Pharmacology, vol. 148, no. 3, pp. 314–325, 2006. View at Publisher · View at Google Scholar · View at Scopus
  22. Z. Hou and J. Zhu, “An experimental study about the incorrect electrophysiological evaluation following peripheral nerve injury and repair,” Electromyography and Clinical Neurophysiology, vol. 38, no. 5, pp. 301–304, 1998. View at Google Scholar · View at Scopus