@2024 Afarand., IRAN
ISSN: 2252-0805 The Horizon of Medical Sciences 2014;20(3):151-156
ISSN: 2252-0805 The Horizon of Medical Sciences 2014;20(3):151-156
Neuroprotective Effect of Alcoholic Extract of Salvia chloroleuca Against Neuronal Degeneration of Alpha Motoneurons of Anterior Horn Spinal Cord after Sciatic Nerve Injury in Rats
ARTICLE INFO
Article Type
Original ResearchAuthors
Razavi M. (1 )Tehranipour M. (* )
Khayatzadeh J. (1 )
(* ) Biology Department, Basic Sciences Faculty, Mashhad Branch, Islamic Azad University, Mashhad, Iran
(1 ) Biology Department, Basic Sciences Faculty, Mashhad Branch, Islamic Azad University, Mashhad, Iran
Correspondence
Address: Biology Department, Basic Sciences Faculty, Islamic Azad University of Mashhad, Rahnama’ei Street, Mashhad, IranPhone: +985138435050
Fax: +985138435050
maryam_tehranipour@mshdiau.ac.ir
Article History
Received: October 18, 2012Accepted: July 16, 2014
ePublished: September 23, 2014
ABSTRACT
Aims
Any damages to the nerve fiber blocking connection with the neurons cell body (vital
cell substances synthesis part), can lead to degenerative changes in proximal and distal parts
of the damaged neuron. Some plants due to the antioxidant substances are effective in the
survival and division of the neurons. This study aimed to investigate the effect of alcoholic
extract of Salvia chloroleuca leaves on destruction of spinal cord anterior horn alpha
motoneurons after sciatic nerve injury in rats.
Materials & Methods In this experimental study 24 male Wistar rats aged 12weeks and weighting 200-250gr were provided. The animals were divided into 4 (each=6) control, damaged, damaged + treatment with 50mg/kg alcoholic extract and damaged+treatment with 75mg/kg alcohol extract groups. To calculate the alpha motoneurons in the anterior horn of the spinal cord in the right side the dissector method was used. Data were analyzed using Minitab 13 software by independent T and ANOVA tests.
Findings The mean density of alpha motoneurons in spinal anterior horn in control group was 1711.5±47.4, in damaged was 730.7±33.4, in damaged+treatment with 50mg/ kg alcoholic extract was 1211.2±34.8 and in damaged+treatment with 75mg/kg alcoholic extract was 987.4±36.8. Mean difference between both treatment groups and damaged group was significant (p=0.001).
Conclusion Salvia chloroleuca leaf extract increases the density of alpha motor neurons in the anterior horn of the spinal cord in rats with sciatic nerve injury, and this increase in neuronal density is associated with the intake of the extract.
Materials & Methods In this experimental study 24 male Wistar rats aged 12weeks and weighting 200-250gr were provided. The animals were divided into 4 (each=6) control, damaged, damaged + treatment with 50mg/kg alcoholic extract and damaged+treatment with 75mg/kg alcohol extract groups. To calculate the alpha motoneurons in the anterior horn of the spinal cord in the right side the dissector method was used. Data were analyzed using Minitab 13 software by independent T and ANOVA tests.
Findings The mean density of alpha motoneurons in spinal anterior horn in control group was 1711.5±47.4, in damaged was 730.7±33.4, in damaged+treatment with 50mg/ kg alcoholic extract was 1211.2±34.8 and in damaged+treatment with 75mg/kg alcoholic extract was 987.4±36.8. Mean difference between both treatment groups and damaged group was significant (p=0.001).
Conclusion Salvia chloroleuca leaf extract increases the density of alpha motor neurons in the anterior horn of the spinal cord in rats with sciatic nerve injury, and this increase in neuronal density is associated with the intake of the extract.
CITATION LINKS
[1]Sunderland S. Nerve Injuries and their repair: A critical appraisal. London: Churchill Livingstone. 1991.
[2]Kerschensteiner M, Schwab ME, Lichtman JW, Misgeld T. In vivo imaging of axonal degeneration and regeneration in the injured spinal cord. Nat Med. 2005;11(5):572-7.
[3]Dahlin LB. Techniques of peripheral nerve repair. Scand J Surg. 2008;97(4):310-6.
[4]Yin Q, Kemp GJ, Frostick SP. Neurotrophins, neurones and peripheral nerve regeneration. J Hand Surg Br. 1998;23(4):433-7.
[5]Janicsak G, Zupko I, Nikolovac MT, Forgo P, Vasas A, Mathe I. Bioactivity-guided study of anti-proliferative activities of Salvia extracts. Nat Prod Commun.2011;6(5):575-9.
[6]Ahmed B, Al-Howiriny T, Al-Rehaily A, Mossa J. Verbenacine and salvinine: two new diterpenes from Salvia verbenaca. Z Naturforsch C. 2004;59(1-2):9-14.
[7]Asadi S, khodagholi F, Esmaeili MA, Khoramian Tusi S, Ansari N, et al. Chemical composition analysis, antioxidant, antiglycating activities and neuroprotective effect of S. chloroleuca, S. mirzayanii and S. santolinifolia from Iran. Am J chin Med. 2011;39(3):615-38.
[8]Yousefzadi M, Sonboli A, Ebrahimi SN, Hashemi SH. Antimicrobial activity of essential oil and major constituents of Salvia chloroleuca. Z Naturforsch C. 2008;63(5-6):337-40.
[9]Ali Shahi Nourani F, Sefidkon F, Yousefzadi M, Nemati S, Khajepiri M. Investigation of chemical compositions and anti-microbial effects of essential oils of Nepeta fissa. Iran J Med Aromat Plants. 2005;21(4):435-64.
[10]Khaliazadeh MA, Esmaeili A, Rustaiyan A, Eslami B, Masoudi Sh. Chemical composition of essential oils of three Salvia species growing wild in Iran. Chem Nat Comp. 2011;46(6):985-7.
[11]Haznedaroglu MZ, Karabay NU, Zeybek U. Antibacterial activity of Salvia tomentosa essential oil. Fitoterapia. 2001;72(7):829-31.
[12]Imanshahidi M, Hosseinzadeh H. The pharmacological effects of Salvia species on the central nervous system. Phytother Res. 2006;20(6):427-37.
[13]Paknejadi M, Foroohi F, Yousefzadi M. Antimicrobial activities of the essential oils of five Salvia species from Tehran province, Iran. J Param Sci. 2012;3(2):12-8.
[14]Cho JY, Chang HJ, Lee SK, Kim HJ, Hwang JK, Chun HS. Amelioration of dextran sulfate sodium-induced colitis in mice by oral administration of beta-caryophyllene, a sesquiterpene. Life Sci. 2007;80(10):932-9.
[15]Juergens UR, Dethlefsen U, Steinkamp G, Gillissen A, Repges R, Vetter H. Anti-inflammatory activity of 1.8-cineol (eucalyptol) in bronchial asthma: A double-blind placebo-controlled trial. Respir Med. 2003;97(3):250-6.
[16]Behnam-Rasouli M, Nikravesh MR, Mahdavi-Shahri N, Tehranipour M. Post-operative time effects after sciatic nerve crush on the number of alpha motoneurons, using a stereological (Disector). Iran Biomed J. 2000;4(1):45-9.
[17]Tehranipour M, Ghadamyari T. The effects of root aquatic extract of Salvia staminea on neuronal density of alpha motoneurons in spinal cord anterior horn after sciatic nerve compression in rats. J Biol Sci. 2010;10(1):48-52.
[18]Kiernan J. Histological and histochemical methods: Theory and practice. 4th ed. New York: Cold Spring Harbor Laboratory Press. 2008;214-39.
[19]Kinugasa T, Ozaki S, Hamanaka S, Kudo N. The effects of sciatic nerve axotomy on spinal motoneurons in neonatal Bax-deficient mice. Neurosci Res. 2002;44(4):439-46.
[20]Nesic O, Xu GY, McAdoo D, High KW, Hulsebosch C, Perez-Pol R. IL-1 receptor antagonist prevents apoptosis and caspase-3 activation after spinal cord injury. J Neurotrauma. 2001;18(9):947-56.
[21]Alamdary SZ, Khodagholi F, Shaerzadeh F, Ansari N, Sonboli A, Tusi SK. S. choloroleuca, S. mirzayanii and S. santolinifolia protect PC12 cells from H2O2-induced apoptosis by blocking the intrinsic pathway. Cytotechnology. 2012;64(4):403-19.
[22]Redshaw JD, Bisby MA. Comparison of the effects of sciatic nerve crush or resection on the proteins of fast axonal transport in rat dorsal root ganglion cell axons. Exp Neurol. 1985;88(2):437-46.
[23]Ghelardini C, Galeotti N, Di Cesare Mannelli L, Mazzanti G, Bartolini A. Local anaesthetic activity of beta-caryophyllene. Farmaco. 2001;56(5-7):387-9.
[24]Santos FA, Rao VS. 1,8-cineol, a food flavoring agent, prevents ethanol-induced gastric injury in rats. Dig Dis Sci. 2001;46(2):331-7.
[25]Landa P, Kokoska L, Pribylova M, Vanek T, Marsik P. In vitro anti-inflammatory activity of carvacrol: Inhibitory effect on COX-2 catalyzed prostaglandin E(2) biosynthesis. Arch Pharm Res. 2009;32(1):75-8.
[26]Cavalcante Melo FH, Rios ER, Rocha NF, Citó Mdo C, Fernandes ML, de Sousa DP, de Vasconcelos SM, de Sousa FC. Antinociceptive activity of carvacrol (5-isopropyl-2-methylphenol) in mice. J Pharm Pharmacol. 2012;64(12):1722-9.
[27]Melo FH, Moura BA, de Sousa DP, de Vasconcelos SM, Macedo DS, Fonteles MM, Viana GS, de Sousa FC. Antidepressant-like effect of carvacrol (5-Isopropyl-2-methylphenol) in mice: involvement of dopaminergic system. Fundam Clin Pharmacol. 2011;25(3):362-7.
[28]Ferrer I, Planas AM. Signaling of cell death and cell survival following focal cerebral ischemia: Life and death struggle in the penumbra. J Neuropathol Exp Neurol. 2003;62(4):329-39.
[29]Baser KH. Biological and pharmacological activities of carvacrol and carvacrol bearing essential oils. Curr Pharm Des. 2008;14(29):3106-19.
[2]Kerschensteiner M, Schwab ME, Lichtman JW, Misgeld T. In vivo imaging of axonal degeneration and regeneration in the injured spinal cord. Nat Med. 2005;11(5):572-7.
[3]Dahlin LB. Techniques of peripheral nerve repair. Scand J Surg. 2008;97(4):310-6.
[4]Yin Q, Kemp GJ, Frostick SP. Neurotrophins, neurones and peripheral nerve regeneration. J Hand Surg Br. 1998;23(4):433-7.
[5]Janicsak G, Zupko I, Nikolovac MT, Forgo P, Vasas A, Mathe I. Bioactivity-guided study of anti-proliferative activities of Salvia extracts. Nat Prod Commun.2011;6(5):575-9.
[6]Ahmed B, Al-Howiriny T, Al-Rehaily A, Mossa J. Verbenacine and salvinine: two new diterpenes from Salvia verbenaca. Z Naturforsch C. 2004;59(1-2):9-14.
[7]Asadi S, khodagholi F, Esmaeili MA, Khoramian Tusi S, Ansari N, et al. Chemical composition analysis, antioxidant, antiglycating activities and neuroprotective effect of S. chloroleuca, S. mirzayanii and S. santolinifolia from Iran. Am J chin Med. 2011;39(3):615-38.
[8]Yousefzadi M, Sonboli A, Ebrahimi SN, Hashemi SH. Antimicrobial activity of essential oil and major constituents of Salvia chloroleuca. Z Naturforsch C. 2008;63(5-6):337-40.
[9]Ali Shahi Nourani F, Sefidkon F, Yousefzadi M, Nemati S, Khajepiri M. Investigation of chemical compositions and anti-microbial effects of essential oils of Nepeta fissa. Iran J Med Aromat Plants. 2005;21(4):435-64.
[10]Khaliazadeh MA, Esmaeili A, Rustaiyan A, Eslami B, Masoudi Sh. Chemical composition of essential oils of three Salvia species growing wild in Iran. Chem Nat Comp. 2011;46(6):985-7.
[11]Haznedaroglu MZ, Karabay NU, Zeybek U. Antibacterial activity of Salvia tomentosa essential oil. Fitoterapia. 2001;72(7):829-31.
[12]Imanshahidi M, Hosseinzadeh H. The pharmacological effects of Salvia species on the central nervous system. Phytother Res. 2006;20(6):427-37.
[13]Paknejadi M, Foroohi F, Yousefzadi M. Antimicrobial activities of the essential oils of five Salvia species from Tehran province, Iran. J Param Sci. 2012;3(2):12-8.
[14]Cho JY, Chang HJ, Lee SK, Kim HJ, Hwang JK, Chun HS. Amelioration of dextran sulfate sodium-induced colitis in mice by oral administration of beta-caryophyllene, a sesquiterpene. Life Sci. 2007;80(10):932-9.
[15]Juergens UR, Dethlefsen U, Steinkamp G, Gillissen A, Repges R, Vetter H. Anti-inflammatory activity of 1.8-cineol (eucalyptol) in bronchial asthma: A double-blind placebo-controlled trial. Respir Med. 2003;97(3):250-6.
[16]Behnam-Rasouli M, Nikravesh MR, Mahdavi-Shahri N, Tehranipour M. Post-operative time effects after sciatic nerve crush on the number of alpha motoneurons, using a stereological (Disector). Iran Biomed J. 2000;4(1):45-9.
[17]Tehranipour M, Ghadamyari T. The effects of root aquatic extract of Salvia staminea on neuronal density of alpha motoneurons in spinal cord anterior horn after sciatic nerve compression in rats. J Biol Sci. 2010;10(1):48-52.
[18]Kiernan J. Histological and histochemical methods: Theory and practice. 4th ed. New York: Cold Spring Harbor Laboratory Press. 2008;214-39.
[19]Kinugasa T, Ozaki S, Hamanaka S, Kudo N. The effects of sciatic nerve axotomy on spinal motoneurons in neonatal Bax-deficient mice. Neurosci Res. 2002;44(4):439-46.
[20]Nesic O, Xu GY, McAdoo D, High KW, Hulsebosch C, Perez-Pol R. IL-1 receptor antagonist prevents apoptosis and caspase-3 activation after spinal cord injury. J Neurotrauma. 2001;18(9):947-56.
[21]Alamdary SZ, Khodagholi F, Shaerzadeh F, Ansari N, Sonboli A, Tusi SK. S. choloroleuca, S. mirzayanii and S. santolinifolia protect PC12 cells from H2O2-induced apoptosis by blocking the intrinsic pathway. Cytotechnology. 2012;64(4):403-19.
[22]Redshaw JD, Bisby MA. Comparison of the effects of sciatic nerve crush or resection on the proteins of fast axonal transport in rat dorsal root ganglion cell axons. Exp Neurol. 1985;88(2):437-46.
[23]Ghelardini C, Galeotti N, Di Cesare Mannelli L, Mazzanti G, Bartolini A. Local anaesthetic activity of beta-caryophyllene. Farmaco. 2001;56(5-7):387-9.
[24]Santos FA, Rao VS. 1,8-cineol, a food flavoring agent, prevents ethanol-induced gastric injury in rats. Dig Dis Sci. 2001;46(2):331-7.
[25]Landa P, Kokoska L, Pribylova M, Vanek T, Marsik P. In vitro anti-inflammatory activity of carvacrol: Inhibitory effect on COX-2 catalyzed prostaglandin E(2) biosynthesis. Arch Pharm Res. 2009;32(1):75-8.
[26]Cavalcante Melo FH, Rios ER, Rocha NF, Citó Mdo C, Fernandes ML, de Sousa DP, de Vasconcelos SM, de Sousa FC. Antinociceptive activity of carvacrol (5-isopropyl-2-methylphenol) in mice. J Pharm Pharmacol. 2012;64(12):1722-9.
[27]Melo FH, Moura BA, de Sousa DP, de Vasconcelos SM, Macedo DS, Fonteles MM, Viana GS, de Sousa FC. Antidepressant-like effect of carvacrol (5-Isopropyl-2-methylphenol) in mice: involvement of dopaminergic system. Fundam Clin Pharmacol. 2011;25(3):362-7.
[28]Ferrer I, Planas AM. Signaling of cell death and cell survival following focal cerebral ischemia: Life and death struggle in the penumbra. J Neuropathol Exp Neurol. 2003;62(4):329-39.
[29]Baser KH. Biological and pharmacological activities of carvacrol and carvacrol bearing essential oils. Curr Pharm Des. 2008;14(29):3106-19.