Vol 78, No 1 (2019)
Original article
Published online: 2018-05-28

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Neuroprotective effects of Potentilla fulgens on spinal cord injury in rats: an immunohistochemical analysis

M. Baloğlu1, A. Çetin2, M. C. Tuncer3
Pubmed: 30402877
Folia Morphol 2019;78(1):17-23.

Abstract

Background: This examination was performed to research the advantage of the antioxidant impact of Potentilla fulgens on spinal cord injury (SCI) in rats. 

Materials and methods: In the SCI model of this examination, the tolerably serious lesion was performed at the L1–L2 spinal segmental level. SCI animals were given P. fulgens 400 mg/kg/day, intraperitoneally. At 7 days post-lesion, exploratory rats were executed after intraperitoneal administration 7 ketamine HCL (0.15 mL/100 g body weight). Spinal cord specimens were taken for histological examination or assurance of malondialdehyde (MDA) and glutathione (GSH) levels and myelope- roxidase (MPO) action. SCI caused a remarkable decline in spinal cord GSH content, trailed by noteworthy increments in MDA levels and MPO action. 

Results: Degenerative changes in some multipolar and bipolar nerve cells and pyknotic changes in the nuclei of glial cells were likewise noticed. Remarkable development was seen in cells and vascular structures of P. fulgens treated groups when contrasted with untreated groups. 

Conclusions: Potentilla fulgens application may influence angiogenetic impro- vement in vein endothelial cells, reduce inflammatory cell aggregation by influ- encing cytokine system and may make apoptotic nerve cells and neuroprotective component in glial cells 

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References

  1. Abrams GM, Ganguly K. Management of chronic spinal cord dysfunction. Continuum (Minneap Minn). 2015; 21(1 Spinal Cord Disorders): 188–200.
  2. Abrams MB, Nilsson I, Lewandowski SA, et al. Imatinib enhances functional outcome after spinal cord injury. PLoS One. 2012; 7(6): e38760.
  3. Ahuja CS, Wilson JR, Nori S, et al. Traumatic spinal cord injury. Nat Rev Dis Primers. 2017; 3: 17018.
  4. Barua CC, Yasmin N. Potentilla fulgens: a systematic review on traditional uses, pharmacology and phytochemical study with reference to anticancer activity. J Nat Prod Resour. 2018; 4(1): 162–170.
  5. Bi F, Huang C, Tong J, et al. Reactive astrocytes secrete lcn2 to promote neuron death. Proc Natl Acad Sci U S A. 2013; 110(10): 4069–4074.
  6. Cabrera-Aldana EE, Ruelas F, Aranda C, et al. Methylprednisolone administration following spinal cord injury reduces aquaporin 4 expression and exacerbates edema. Mediators Inflamm. 2017; 2017: 4792932.
  7. Chen MH, Ren QX, Yang WF, et al. Influences of HIF-lα on Bax/Bcl-2 and VEGF expressions in rats with spinal cord injury. Int J Clin Exp Pathol. 2013; 6(11): 2312–2322.
  8. Cho M. Focus on neurodegeneration. Nat Neurosci. 2010; 13(7): 787.
  9. Christie SD, Comeau B, Myers T, et al. Duration of lipid peroxidation after acute spinal cord injury in rats and the effect of methylprednisolone. Neurosurg Focus. 2008; 25(5): E5.
  10. del Rayo Garrido M, Silva-García R, García E, et al. Therapeutic window for combination therapy of A91 peptide and glutathione allows delayed treatment after spinal cord injury. Basic Clin Pharmacol Toxicol. 2013; 112(5): 314–318.
  11. DeRuisseau LR, Recca DM, Mogle JA, et al. Metallothionein deficiency leads to soleus muscle contractile dysfunction following acute spinal cord injury in mice. Am J Physiol Regul Integr Comp Physiol. 2009; 297(6): R1795–R1802.
  12. Fernández R, González P, Lage S, et al. Influence of the cation adducts in the analysis of matrix-assisted laser desorption ionization imaging mass spectrometry data from injury models of rat spinal cord. Anal Chem. 2017; 89(16): 8565–8573.
  13. Fouad K, Tetzlaff W. Rehabilitative training and plasticity following spinal cord injury. Exp Neurol. 2012; 235(1): 91–99.
  14. Genovese T, Esposito E, Mazzon E, et al. Absence of endogenous interleukin-10 enhances secondary inflammatory process after spinal cord compression injury in mice. J Neurochem. 2009; 108(6): 1360–1372.
  15. Genovese T, Esposito E, Mazzon E, et al. Evidence for the role of mitogen-activated protein kinase signaling pathways in the development of spinal cord injury. J Pharmacol Exp Ther. 2008; 325(1): 100–114.
  16. Herrera JJ, Nesic O, Narayana PA. Reduced vascular endothelial growth factor expression in contusive spinal cord injury. J Neurotrauma. 2009; 26(7): 995–1003.
  17. Hillegass LM, Griswold DE, Brickson B, et al. Assessment of myeloperoxidase activity in whole rat kidney. J Pharmacol Methods. 1990; 24(4): 285–295.
  18. Hoschouer EL, Yin FQ, Jakeman LB. L1 cell adhesion molecule is essential for the maintenance of hyperalgesia after spinal cord injury. Exp Neurol. 2009; 216(1): 22–34.
  19. Jaitak V, Kaul VK, Kumar N, et al. New hopane triterpenes and antioxidant constituents from Potentilla fulgens. Nat Prod Commun. 2010; 5(10): 1561–1566.
  20. Jia YF, Gao HL, Ma LJ, et al. Effect of nimodipine on rat spinal cord injury. Genet Mol Res. 2015; 14(1): 1269–1276.
  21. Kanno H, Ozawa H, Sekiguchi A, et al. Spinal cord injury induces upregulation of Beclin 1 and promotes autophagic cell death. Neurobiol Dis. 2009; 33(2): 143–148.
  22. Kopach O, Medvediev V, Krotov V, et al. Opposite, bidirectional shifts in excitation and inhibition in specific types of dorsal horn interneurons are associated with spasticity and pain post-SCI. Sci Rep. 2017; 7(1): 5884.
  23. Koziel K, Smigelskaite J, Drasche A, et al. RAF and antioxidants prevent cell death induction after growth factor abrogation through regulation of Bcl-2 proteins. Exp Cell Res. 2013; 319(17): 2728–2738.
  24. Kundu A, Ghosh A, Singh NK, et al. Wound healing activity of the ethanol root extract and polyphenolic rich fraction from Potentilla fulgens. Pharm Biol. 2016; 54(11): 2383–2393.
  25. Liu Y, Figley S, Spratt SK, et al. An engineered transcription factor which activates VEGF-A enhances recovery after spinal cord injury. Neurobiol Dis. 2010; 37(2): 384–393.
  26. Ludwig PE, Patil AA, Chamczuk AJ, et al. Hormonal therapy in traumatic spinal cord injury. Am J Transl Res. 2017; 9(9): 3881–3895.
  27. Moonen G, Satkunendrarajah K, Wilcox JT, et al. A new acute impact-compression lumbar spinal cord injury model in the rodent. J Neurotrauma. 2016; 33(3): 278–289.
  28. Müller MM, Middelanis J, Meier C, et al. 17β-estradiol protects 7-day old rats from acute brain injury and reduces the number of apoptotic cells. Reprod Sci. 2013; 20(3): 253–261.
  29. Nesic O, Sundberg LM, Herrera JJ, et al. Vascular endothelial growth factor and spinal cord injury pain. J Neurotrauma. 2010; 27(10): 1793–1803.
  30. Özevren H, Irtegün S, Deveci E, et al. Neuroprotective Effects of Potentilla fulgens on traumatic brain injury in rats. Anal Quant Cytol Histol. 2017; 39: 35–44.
  31. Patel CB, Cohen DM, Ahobila-Vajjula P, et al. Effect of VEGF treatment on the blood-spinal cord barrier permeability in experimental spinal cord injury: dynamic contrast-enhanced magnetic resonance imaging. J Neurotrauma. 2009; 26(7): 1005–1016.
  32. Ray SK, Samntaray S, Banik NL. Future directions for using estrogen receptor agonists in the treatment of acute and chronic spinal cord injury. Neural Regen Res. 2016; 11(9): 1418–1419.
  33. Ren Yi, Young W. Managing inflammation after spinal cord injury through manipulation of macrophage function. Neural Plast. 2013; 2013: 945034.
  34. Savas M, Verit A, Ciftci H, et al. Oxidative Stress in BPH. JNMA J Nepal Med Assoc. 2009; 48(173): 41–45.
  35. Shen LF, Cheng H, Tsai MC, et al. PAL31 may play an important role as inflammatory modulator in the repair process of the spinal cord injury rat. J Neurochem. 2009; 108(5): 1187–1197.
  36. Silva NA, Sousa N, Reis RL, et al. From basics to clinical: a comprehensive review on spinal cord injury. Prog Neurobiol. 2014; 114: 25–57.
  37. Sinescu C, Popa F, Grigorean VT, et al. Molecular basis of vascular events following spinal cord injury. J Med Life. 2010; 3(3): 254–261.
  38. Song Z, Xu S, Song B, et al. Bcl-2-associated athanogene 2 prevents the neurotoxicity of MPP+ via interaction with DJ-1. J Mol Neurosci. 2015; 55(3): 798–802.
  39. Sun T, Liu B, Li P. Nerve protective effect of asiaticoside against ischemia-hypoxia in cultured rat cortex neurons. Med Sci Monit. 2015; 21: 3036–3041.
  40. Syiem D, Khup PZ, Syiem AB. Effects of Potentilla fulgens Linn. on carbohydrate and lipid profiles in diabetic mice. Pharmacologyonline. 2009; 2: 787–795.
  41. Tas M, Gok E, Ekinci C, et al. Investigation of Various Events Occurring in the Brain Tissue After Calvarial Defects in Rats. Int J Morphol. 2016; 34(1): 29–33.
  42. Toklu HZ, Hakan T, Celik H, et al. Neuroprotective effects of alpha-lipoic acid in experimental spinal cord injury in rats. J Spinal Cord Med. 2010; 33(4): 401–409.
  43. Tu WZ, Chen WC, Xia W, et al. The regulatory effect of electro-acupuncture on the expression of NMDA receptors in a SCI rat model. Life Sci. 2017; 177: 8–14.
  44. Wu Y, Yang L, Mei X, et al. Selective inhibition of STAT1 reduces spinal cord injury in mice. Neurosci Lett. 2014; 580: 7–11.
  45. Yu YQ, Hu NC, Duan JA, et al. Neuroprotective effects of sufentanil preconditioning on spinal cord injury in mouse models. J Tissue Eng. 2016; 20: 5966–5972.