Effects of Aqueous Extract of Achyranthes Japonica on Functional Recovery in Sciatic Nerve after Crushed Sciatic Nerve Injury in Rats

우슬 추출물이 흰쥐 좌골신경 손상 후 좌골신경의 기능회복에 미치는 영향

  • Lee, Ma-Seong (Dept. of Oriental Rehabilitation Medicine, College of Oriental Medicine, Kyung-Won University) ;
  • Song, Yun-Kyung (Dept. of Oriental Rehabilitation Medicine, College of Oriental Medicine, Kyung-Won University) ;
  • Lim, Hyung-Ho (Dept. of Oriental Rehabilitation Medicine, College of Oriental Medicine, Kyung-Won University)
  • 이마성 (경원대학교 한의과대학 한방재활의학과교실) ;
  • 송윤경 (경원대학교 한의과대학 한방재활의학과교실) ;
  • 임형호 (경원대학교 한의과대학 한방재활의학과교실)
  • Received : 2011.03.15
  • Accepted : 2011.04.14
  • Published : 2011.04.30

Abstract

Objectives : Peripheral nerve injuries are commonly encountered clinical problem and often result in severe functional deficits. The aim of this study is to evaluate the effects of aqueous extract of Achyranthes japonica(AJ) on functional recovery in sciatic nerve after crushed sciatic nerve injury. Methods : In the present study, the animals in the AJ-treated groups received the aqueous extract of AJ at the respective doses orally for 13 consecutive days. In order to assess the effects of the aqueous extract of AJ on function recovery in crushed sciatic nerve injury, sciatic functional index(SFI) was performed. c-Fos expression in the paraventricular nucleus(PVN) and ventrolateral periaqueductal gray(vIPAG), and neurofilament, and the expressions of brain-derived neurotrophic factor(BDNF), nerve growth factor(NGF) following crushed sciatic nerve injury in rats were investigated. For this, immunohistochemistry and western blot were performed. Results : In the present study, crushed sciatic nerve injury showed characteristic gait changes showing decrease of SFI value and treatment with the aqueous extract of AJ significantly enhanced the SFI value. Neurofilament expression in the sciatic nerve was decreased by crushed sciatic nerve injury and treatment with the AJ increased neurofilament expression. The expressions of BDNF and NGF in the sciatic nerve were increased following crushed sciatic nerve injury and treatment with the AJ significantly controlled the sciatic nerve injury-induced increment of BDNF and NGF expressions. c-Fos expressions in the PVN and vIPAG were increased following crushed sciatic nerve injury and treatment with the AJ significantly suppressed the sciatic nerve injury-induced increment of c-Fos expressions. Conclusions : These results suggest that AJ treatment after crushed sciatic nerve injury is effective in the functional recovery by enhancing axonal regeneration and suppressing of pain.

Keywords

Acknowledgement

Supported by : 경원대학교

References

  1. Hyun JK, Lee SJ, Yoo DS, Park HG, Kwon BS. The electrodiagnostic finding of sciatic nerve injury according to the locations and etiologies. J Korean Acad Rehabil Med. 2004;28:54-8.
  2. Park KC, Kim KW, Kim YH. Combined femoral and sciatic nerve palsy associated with acetabular fracture and dislocation-A case report. J. Korean Fracture Soc. 2005;18:341-4. https://doi.org/10.12671/jkfs.2005.18.3.341
  3. Dahlin LD. The biology of nerve injury and repair. J Am Soc Surg Hand. 2004;4:143-55. https://doi.org/10.1016/j.jassh.2004.06.006
  4. Rodella L, Rezzani R, Gioia M, Tredici G, Bianchi R. Expression of Fos immunoreactivity in the rat supraspinal regions following noxious visceral stimulation. Brain Res Bull.. 1998;47:357-66. https://doi.org/10.1016/S0361-9230(98)00123-3
  5. Fu SY, Gordon T. The cellular and molecular basis of peripheral nerve regeneration. Mol Neurobiol. 1997;14:67-116. https://doi.org/10.1007/BF02740621
  6. Cragg BG, Thomas PK. Change in conduction velocity and fiber size proximal to peripheral nerve lesions. J. Physiol.. 1961;157:315-27. https://doi.org/10.1113/jphysiol.1961.sp006724
  7. Schroder JM. Altered ratio between axon diameter and myelin sheath thickness in regenerated nerve fibers. Brain Res. 1972;45:49-65. https://doi.org/10.1016/0006-8993(72)90215-6
  8. 한의과대학 본초학 편찬위원회. 본초학. 서울:영림사. 2004:469-70.
  9. Marcone MF, Jahaniaval F, Aliee H, Kakuda Y. Chemical characterization of Achranthes bidentata seed. Food Chem. 2003;81:7-12. https://doi.org/10.1016/S0308-8146(02)00250-9
  10. Shimomura H, Sashida Y, Nakata H. Plant growth regulationg activities of crude drugs and medicinal plants. Shoyakugaku Zasshi. 1981;5:173-9.
  11. Hyun-Chol Cho, Yun-Kyung Song, Hyung-Ho Lim. Effects of Gentianae Macrophyllae Radix on the functional recovery and expression of BDNF and c-Fos after sciatic crushed nerve injury in rats. The Journal of Korean Oriental Medicine. 2009;30(3):28-38.
  12. Tae-Young Cho, Yun-Kyung Song, Hyung-Ho Lim. The Effects of Aqueous Extracts of Aconiti ciliare tuber on Functional Recovery after sciatic crushed nerve injury in Rats. The Journal of Korean Oriental Medicine. 2009;30(3):39-50.
  13. Moon-Kyu Lee, Yun-Kyung Song, Hyung-Ho Lim. Effects of Acupuncture at GB30, GB34, and BL40 on Functional Recovery after sciatic arushed nerve injury in Rats. The Journal of Korean Oriental Medicine. 2010;31(3):66-78.
  14. Seung-Peom Choi, Yun-Kyung Song, Hyung-Ho Lim. Effects of Bee Venom and Sweet Bee Venom Acupuncture on Functional Recovery and c-Fos Expression in the Brain after sciatic crushed nerve injury in Rats. The Journal of Korean Oriental Medicine. 2010;31(3):79-97.
  15. Ding F, Cheng Q, Gu X. The repair effects of Achyranthes bidentata extract on the crushed common peroneal nerve of rabbits. Fitoterapia. 2008;79:161-7. https://doi.org/10.1016/j.fitote.2007.10.002
  16. Shen H, Yuan Y, Ding F, Liu J, Gu X. The protective effects of Achyranthes bidentata polypeptides against NMDA-induced cell apoptosis in cultured hippocampal neurons through differential modulation of NR2A-and NR2B-containing NMDA receptors. Brain Res Bull. 2008;77:274-81. https://doi.org/10.1016/j.brainresbull.2008.08.002
  17. Bain JR, Mackinnon SE, Hunter DA. Functional evaluation of complete sciatic, peroneal, and posterior tibial nerve lesions in the rat. Plast Reconstr Surg. 1989;83:129-38. https://doi.org/10.1097/00006534-198901000-00024
  18. Kim JC, Choi GJ, Lee SW, Kim JS, Chung KY, Cho KY. Screening extracts of Achyranthes japonica and Rumex crispus for activity against vatious plant pathogenic fungi and control of powdery mildew. Pest Manag Sci. 2004;60:803-8. https://doi.org/10.1002/ps.811
  19. Son KH, Hwang JH, Lee SH, Park JH, Kang SJ, Chang SY, Lee KS. Isolation and quantitative determination of 20-hydroxyecdysone from Achyranthes radix. Korean Journal Pharmacogn. 1999;30:335-9.
  20. Li J, Qi H, Qi LW, Yi L, Li P. Simultaneous determination of main phytoecdysones and triterpenoids in radix achyranthis bidentatae by high-performance liquid chromatography with diode array-evaporative light scattering detectors and mass spectrometry. Anal Chim Acta. 2007;596:264-72. https://doi.org/10.1016/j.aca.2007.05.016
  21. Chen XM, Tian GY. Structural elucidation and antitumor activity of a fructaan from Cyathula officinalis Kuan. Carbohydr Res. 2003;338:1235-41. https://doi.org/10.1016/S0008-6215(03)00073-9
  22. 김주호, 기지예, 안지영, 박혜정, 김현주, 곽한복, 오재만, 김윤경. 우슬의 파골세포 분화 억제와 골 흡수 억제효과. 대한본초학회지. 2010;25(1):66-74.
  23. 김영옥, 이상원, 이승은. Carrageenan으로 유발한 관절염 쥐에서의 우슬추출물 효과. 한국약용작물학회지. 2009;17(6):470-4.
  24. 박재상, 성낙술, 이영종. 우슬, 회우슬 및 천우슬의 산화억제 효과 비교 연구. 대한본초학회지. 2007;22(4):155-67.
  25. 김성진, 박준봉, 권영혁, 박건구, 정세영. 우슬추출물의 경조직 재생 촉진효과. 한국응용약물학회지. 2002;10:253-7.
  26. de Medinaceli L, Freed WJ, Wyatt RJ. An index of the functional condition of rat sciatic nerve based on measurements made from walking tracks. Exp Neurol. 1982;77:634-43. https://doi.org/10.1016/0014-4886(82)90234-5
  27. Rahul K, Tessa AH. Quantification of functional recovery following rat sciatic nerve transection. Exp Neurol. 2000;168:192-5.
  28. Fawcett JW, Keynes RJ. Peripheral nerve regeneration. Annu Rev Neurosci. 1990;13:43-60. https://doi.org/10.1146/annurev.ne.13.030190.000355
  29. Lefcort F, Venstrom K, McDonald JA, Reichardt LF. Regulation of expression of fibronectin and its receptor, 51, during development and generation of peripheral nerve. Development. 1992;116:767-82.
  30. Nieke J, Schachner M. Expression of the neural cell adhesion molecules L1 and N-CAM and their common carbohydrate epitope L2/HNK-1 during development and after transection of the mouse sciatic nerve. Differentitation. 1985;30:141-51. https://doi.org/10.1111/j.1432-0436.1985.tb00525.x
  31. Barde YA, Edgar D, Thoenen H. Purification of a new neurotrophic factor from mammalian brain. EMBO J. 1982:549-53.
  32. Klintsova AY, Greenough WT. Synaptic plasticity in cortical systems. Curr Opin Neurobiol. 1999;9:203-8. https://doi.org/10.1016/S0959-4388(99)80028-2
  33. Zhang JY, Luo XG, Xian CJ, Liu ZH, Zhou XF. Endogenous BDNF is required for myelination and regeneration of injured sciatic nerve in rodents. Eur J Neurosci. 2000;12:4171-80.
  34. Kanaya F, Firrell JC, Bbreidenbach WC. Sciatic function index, nerve conduction tests, muscle contraction, and axon morphometry as indicators of regeneration. Plast Reconstr Surg. 1996;98:1264-71. https://doi.org/10.1097/00006534-199612000-00023
  35. Meyer M, Matsuoka I, Wetmore C, Olson L, Thoenen H. Enhanced synthesis of brain-derived neurotrophic factor in the lesioned peripheral nerve: different mechanisms are responsible for the regulation of BDNF and NGF mRNA. J Cell Biol. 1992;119:45-54 https://doi.org/10.1083/jcb.119.1.45
  36. Heumann R, Korsching S, Bandtlow C, Thoenen H. Changes of nerve growth factor synthesis in nonneuronal cells in response to sciatic nerve transection. J Cell Biol. 1987;104:1623-31. https://doi.org/10.1083/jcb.104.6.1623
  37. Barres BA, Raff MC, Gaese F, Bartke I, Dechant G, Barde YA. A crucial role for neurotrophin-3 in oligodendrocyte development. Nature. 1994;367:371-5. https://doi.org/10.1038/367371a0
  38. Johnson EM, Barde YA, Schwwab M, Thoenen H. Brain-derived neurotrophic factor supports the survival of cultures rat retinal ganglion cells. J Neurosci. 1986;6:3031-8. https://doi.org/10.1523/JNEUROSCI.06-10-03031.1986
  39. Stockel K, Solomon F, Paravicini U, Thoenen H. Dissociation between effects of nerve growth factor on tyrosine hydroxylase and tubulin synthesis in sympathetic ganglia. Nature. 1974;250:150-1. https://doi.org/10.1038/250150a0
  40. Stockel K, Schwab M, Thoenen H. Comparison between the retrograde axonal transport of nerve growth factor and tetanus toxin in motor, sensory and adrenergic neurons. Brain Res. 1975;99:1-16. https://doi.org/10.1016/0006-8993(75)90604-6
  41. Sobue G, Yamamoto M, Doyu M, Li M, Yasuda T, Mitsuma T. Expression of mRNAs for neurotrophins(NGF, BDNF, and NT-3) and their receptors(p75NGFR, trk, trkB, and trkC) in human peripheral neuropathies. Neurochem Res. 1998;23:821-9. https://doi.org/10.1023/A:1022434209787
  42. Leibrock J, Lottspeich F, Hohn A, Hengerer B, Masiakowski P, Thoenen H, Barde YA. Molecular cloning and expression of brain-derived neurotrophic factor. Nature. 1989;341:149-52. https://doi.org/10.1038/341149a0
  43. Lindsay RM, Thoenen H, Barde YA. Placode and neural crestderived sensory neurons are responsive at early developmental stages to brain-derived neurotrophic factor. Dev Biol. 1985;112:319-28. https://doi.org/10.1016/0012-1606(85)90402-6
  44. Maisonpierre PC, Belluscio L, Squito S, Ip NY, Furth ME, Lindsay RM, Yancopoulos GD. Neurotrophin-3: A neurotrophic factor related to NGF and BDNF. Science. 1990;247:1446-51. https://doi.org/10.1126/science.2321006
  45. Cho HJ, Kim JK, Zhou XF, Rush RA. Increased brain-derived neurotrophic factor immunoreactivity in rat dorsal root ganglia and spinal cord following peripheral inflammation. Brain Res. 1997;764:269-72. https://doi.org/10.1016/S0006-8993(97)00597-0
  46. Lee SL, Kim JK, Kim DS, Cho HJ. Expression of mRNAs encoding full-length and truncated TrkB receptors in rat dorsal root ganglia and spinal cord following peripheral inflammation. Neuroreport. 1999;10:2847-51. https://doi.org/10.1097/00001756-199909090-00027
  47. Weskamp G, Otten U. An enzyme-linked immunoassay for nerve growth factor(NGF): a tool for studying regulatory mechanisms involved in NGF production in brain and in peripheral tissues. J Neurochem. 1987;48:1779-86. https://doi.org/10.1111/j.1471-4159.1987.tb05736.x
  48. Wild KD, Bian D, Zhu D, Davis J, Bannon AW, Zhang TJ, Louis JC. Antibodies to nerve growth factor reverse established tactile allodynia in rodent models of neuropathic pain without tolerance. J Pharmacol Exp Ther. 2007;322:282-7. https://doi.org/10.1124/jpet.106.116236
  49. Zhou XF, Deng YS, Xian CJ, Zhong JH. Neurotrophins from dorsal root ganglia trigger allodynia after spinal nerve injury in rats. Eur Journal Neurosci. 2000;12:100-5. https://doi.org/10.1046/j.1460-9568.2000.00884.x
  50. Brooks D, Panthaki Z, Buncke HJ, Buncke GM. Neuroma transposition and intramuscular implantation using the Mitek "soft-tissue anchor": a new technique. Ann Plast Surg. 2001;47:257-62. https://doi.org/10.1097/00000637-200109000-00007
  51. Kryger GS, Kryger Z, Zhang F, Shelton DL, Lineaweaver WC, Buncke HJ. Nerve growth factor inhibition prevents traumatic neuroma formation in the rat. J Hand Surg Am. 2001;26:635-44. https://doi.org/10.1053/jhsu.2001.26035
  52. Ziff EB. Transcription factors: a new family gathers at the c AMP response site. Trends Genet. 1990;6:69-72. https://doi.org/10.1016/0168-9525(90)90081-G
  53. Bellchambers CE, Chieng B, Keay KA, Christie MJ. Swim-stress but not opioid withdrawal increases expression of c-fos immunoreactivity in rat periaqueductal gray neurons which project to the rostral ventromedial medulla. Neuroscience. 1998;83:517-24. https://doi.org/10.1016/S0306-4522(97)00399-0
  54. Lee TH, Jang MH, Shin MC, Lim BV, Kim YP, Kim H, Choi HH, Lee KS, Kim EH, Kim CJ. Dependence of rat hippocampal c-Fos expression on intensity and duration of exercise. Life Sci. 2003;72:1421-36. https://doi.org/10.1016/S0024-3205(02)02406-2
  55. Min JH, Park CM, Moon DE, Kim SN, Chung CW, Kim KH. Fos expression in the brain of neuropathic pain rats. Korean Journal Anesthesiol. 2001;41:229-37. https://doi.org/10.4097/kjae.2001.41.2.229
  56. Bullitt E. Expression of c-Fos like protein as a marker for neuronal activity following noxious stimulation in the rat. J Comp Neurol. 1990;296:517-30. https://doi.org/10.1002/cne.902960402
  57. Rodriguez FJ, Cabre AV, Navarro X. Regeneration and functional recovery following peripheral nerve injury. Drug Discov Today. 2004;1:177-85.
  58. Narita M, Ozaki S, Narita M, Ise Y, Yajima Y, Suzuki T. Change in the expression of c-Fos in the rat brain following sciatic nerve ligation. Neurosci Lett. 2003;352:231-3. https://doi.org/10.1016/j.neulet.2003.08.052