Intracerebroventricular injection of propranolol blocked analgesic and neuroprotective effects of resveratrol following L


Journal

Journal of complementary & integrative medicine
ISSN: 1553-3840
Titre abrégé: J Complement Integr Med
Pays: Germany
ID NLM: 101313855

Informations de publication

Date de publication:
10 May 2021
Historique:
received: 25 09 2020
accepted: 02 01 2021
pubmed: 8 5 2021
medline: 29 12 2021
entrez: 7 5 2021
Statut: epublish

Résumé

Resveratrol as a natural polyphenolic agent can alleviate neuropathic pain symptoms. The mechanism of analgesic activity of resveratrol is far from clear. The current study examine whether analgesic activity of resveratrol is mediated by its neuroprotective and anti-oxidant activity in the neuropathic pain. We further examine whether analgesic activity of resveratrol is mediated by β-adrenoceptors in the brain. Neuropathic pain induced by L Resveratrol significantly decreased thermal allodynia (and not anxiety) in all experimental days. Additionally, resveratrol significantly increased NCV, and also normalized the disrupted Cat and SOD activities following neuropathic pain. Furthermore, propranolol significantly blocked the analgesic and neuroprotective effects of resveratrol. It is suggested that the analgesic effects of resveratrol is mediated by its neuroprotective and antioxidant activities in the neuropathic rats. Furthermore, propranolol blocked the analgesic and neuroprotective effects of resveratrol.

Identifiants

pubmed: 33962501
pii: jcim-2020-0393
doi: 10.1515/jcim-2020-0393
doi:

Substances chimiques

Analgesics 0
Neuroprotective Agents 0
Propranolol 9Y8NXQ24VQ
Resveratrol Q369O8926L

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

701-710

Informations de copyright

© 2021 Walter de Gruyter GmbH, Berlin/Boston.

Références

Garg, G, Adams, JD. Treatment of neuropathic pain with plant medicines. Chin J Integr Med 2012;18:565–70. https://doi.org/10.1007/s11655-012-1188-6.
Ferreira-Chamorro, P, Redondo, A, Riego, G, Leánez, S, Pol, O. Sulforaphane inhibited the nociceptive responses, anxiety- and depressive-like behaviors associated with neuropathic pain and improved the anti-allodynic effects of morphine in mice. Front Pharmacol 2018;9:1332. https://doi.org/10.3389/fphar.2018.01332.
Chen, H, Hu, Y, Xie, K, Chen, Y, Wang, H, Bian, Y, et al.. Effect of autophagy on allodynia, hyperalgesia and astrocyte activation in a rat model of neuropathic pain. Int J Mol Med 2018;42:2009–19. https://doi.org/10.3892/ijmm.2018.3763.
Shahid, M, Subhan, F, Ahmad, N, Ullah, I. A bacosides containing Bacopa monnieri extract alleviates allodynia and hyperalgesia in the chronic constriction injury model of neuropathic pain in rats. BMC Compl Alternative Med 2017;17:293. https://doi.org/10.1186/s12906-017-1807-z.
Kline, RH, Exposto, FG, O’Buckley, SC, Westlund, KN, Nackley, AG. Catechol-O-methlytransferase inhibition alters pain and anxiety-related volitional behaviors through activation of β-adrenergic receptors in the rat. Neuroscience 2015;290:561–69. https://doi.org/10.1016/j.neuroscience.2015.01.064.
Ciszek, BP, O’Buckley, SC, Nackley, AG. Persistent COMT-dependent pain is initiated by peripheral, but not spinal or central, β2- and β3- adrenergic receptors. Anesthesiology 2016;124:1122–35. https://doi.org/10.1097/aln.0000000000001070.
Choucair-Jaafar, N, Yalcin, I, Rodeau, JL, Waltisperger, E, Freund-Mercier, MJ, Barrot, M. Beta2-adrenoceptor agonists alleviate neuropathic allodynia in mice after chronic treatment. Br J Pharmacol 2009;158:1683–94. https://doi.org/10.1111/j.1476-5381.2009.00510.x.
Khasar, SG, McCarter, G, Levine, JD. Epinephrine produces a beta-adrenergic receptor-mediated mechanical hyperalgesia and in vitro sensitization of rat nociceptors. J Neurophysiol 1999;81:1104–12. https://doi.org/10.1152/jn.1999.81.3.1104.
Pertovaara, A. The noradrenergic pain regulation system: a potential target for pain therapy. Eur J Pharmacol 2013;716:1–7. https://doi.org/10.1016/j.ejphar.2013.01.067.
Zhang, TT, Xue, R, Zhu, L, Li, J, Fan, QY, Zhong, BH, et al.. Evaluation of the analgesic effects of ammoxetine, a novel potent serotonin and norepinephrine reuptake inhibitor. Acta Pharmacol Sin 2016;37:1154–65. https://doi.org/10.1038/aps.2016.45.
Caraci, F, Merlo, S, Drago, F, Caruso, G, Parenti, C, Sortino, MA. Rescue of noradrenergic system as a novel pharmacological strategy in the treatment of chronic pain: focus on microglia activation. Front Pharmacol 2019;10:1024. https://doi.org/10.3389/fphar.2019.01024.
Safakhah, HA, Taghavi, T, Rashidy-Pour, A, Vafaei, AA, Sokhanvar, M, Mohebbi, N, et al.. Effects of saffron (Crocus sativus L.) stigma extract and its active constituent crocin on neuropathic pain responses in a rat model of chronic constriction injury. Iran J Pharm Res 2016;15:253–61.
Chien, MY, Ku, YH, Chang, JM, Yang, CM, Chen, CH. Effects of herbal mixture extracts on obesity in rats fed a high-fat diet. J Food Drug Anal 2016;24:594–601. https://doi.org/10.1016/j.jfda.2016.01.012.
Park, JP, Kim, JH, Park, MK, Yu, JW. Potential agents for cancer and obesity treatment with herbal medicines from the green garden. Biotechnol Bioproc Eng 2011;16:1065–76. https://doi.org/10.1007/s12257-011-0215-3.
Wang, G, Hu, Z, Song, X, Cui, Q, Fu, Q, Jia, R, et al.. Analgesic and anti-inflammatory activities of resveratrol through classic models in mice and rats. Evid Based Complement Alternat Med 2017;2017:5197567. https://doi.org/10.1155/2017/5197567.
Feng, Y, Cui, Y, Gao, JL, Li, R, Jiang, XH, Tian, YX, et al.. Neuroprotective effects of resveratrol against traumatic brain injury in rats: involvement of synaptic proteins and neuronal autophagy. Mol Med Rep 2016;13:5248–54. https://doi.org/10.3892/mmr.2016.5201.
AlBasher, G, Abdel-Daim, MM, Almeer, R, Ibrahim, KA, Hamza, RZ, Bungau, S, et al.. Synergistic antioxidant effects of resveratrol and curcumin against fipronil-triggered oxidative damage in male albino rats. Environ Sci Pollut Res Int 2020;27:6505–14. https://doi.org/10.1007/s11356-019-07344-8.
Guo, J, Wang, C, Niu, X, Zhou, F, Li, H, Gao, W. Effects of resveratrol in the signaling of neuropathic pain involving P2X3 in the dorsal root ganglion of rats. Acta Neurol Belg 2019;2019.
de Sá Coutinho, D, Pacheco, MT, Frozza, RL, Bernardi, A. Anti-inflammatory effects of resveratrol: mechanistic insights. Int J Mol Sci 2018;19:1812. https://doi.org/10.3390/ijms19061812.
Yuan, Y, Zhen, L, Li, Z, Xu, W, Leng, H, Xu, W, et al.. Trans-resveratrol ameliorates anxiety-like behaviors and neuropathic pain in mouse model of post-traumatic stress disorder. J Psychopharmacol 2020;34:726–36. https://doi.org/10.1177/0269881120914221.
Kumar, A, Naidu, PS, Seghal, N, Padi, SSV. Neuroprotective effects of resveratrol against intracerebroventricular colchicine-induced cognitive impairment and oxidative stress in rats. Pharmacology 2007;79:17–26. https://doi.org/10.1159/000097511.
Qi, Y, Shang, L, Liao, Z, Su, H, Jing, H, Wu, B, et al.. Intracerebroventricular injection of resveratrol ameliorated Aβ-induced learning and cognitive decline in mice. Metab Brain Dis 2019;34:257–66. https://doi.org/10.1007/s11011-018-0348-6.
Kim, SH, Chung, JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain 1992;50:355–63.
Mirasheh, MH, Zohrehvand, MR, Kazemi, R, Bahari, Z, Bahrami, F, Jangravi, Z, et al.. The analgesic and anxiolytic activity of resveratrol mediated by different sub-types of α-adrenoceptors of anterior cingulate cortex following neuropathic pain in male rats. J Adv Med Biomed Res 2020;28:183–90. https://doi.org/10.30699/jambs.28.129.183.
Wang, YX, Mao, XF, Li, TF, Gong, N, Zhang, MZ. Dezocine exhibits antihypersensitivity activities in neuropathy through spinal μ-opioid receptor activation and norepinephrine reuptake inhibition. Sci Rep 2017;7:43137. https://doi.org/10.1038/srep43137.
Liu, Y, Dong, R, Zhang, C, Yang, Y, Xu, Y, Wang, H, et al.. Therapeutic effects of nerve leachate-treated adipose-derived mesenchymal stem cells on rat sciatic nerve injury. Exp Ther Med 2020;19:223–31.
Bradford, MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248–54. https://doi.org/10.1016/0003-2697(76)90527-3.
Aebi, H. Catalase in vitro. Methods Enzymol 1984;105:121–6. https://doi.org/10.1016/s0076-6879(84)05016-3.
Namadr, F, Bahrami, F, Bahari, Z, Ghanbari, B, Elahi, SA, Mohammadi, MT. Evaluation of the effects of fullerene C60 nanoparticles on oxidative stress parameters in normal rats liver and brain. J Adv Med Biomed Res 2019;27:8–15.
Parent, AJ, Beaudet, N, Beaudry, H, Bergeron, J, Bérubé, P, Drolet, G, et al.. Increased anxiety-like behaviors in rats experiencing chronic inflammatory pain. Behav Brain Res 2012;229:160–7. https://doi.org/10.1016/j.bbr.2012.01.001.
Cui, Y, Li, Y, Ning, J, Mi, Y, Wang, X, Qiu, Z, et al.. Resveratrol alleviates diabetic mechanical allodynia in rats by downregulating P2X3R. Mol Med Rep 2020;22:957–63. https://doi.org/10.3892/mmr.2020.11157.
Yin, Q, Lu, FF, Zhao, Y, Cheng, MY, Fan, Q, Cui, J, et al.. Resveratrol facilitates pain attenuation in a rat model of neuropathic pain through the activation of spinal Sirt1. Reg Anesth Pain Med 2013;38:93–9. https://doi.org/10.1097/aap.0b013e3182795b23.
Zeinali, H, Manaheji, H, Zaringhalam, J, Bahari, Z, Nazemi, S, Sadeghi, M. Age-related differences in neuropathic pain behavior and spinal microglial activity after L5 spinal nerve ligation in male rats. BCN 2016;7:203–12. https://doi.org/10.15412/j.bcn.03070305.
Singh, H, Bhushan, S, Arora, R, Buttar, HS, Arora, S, Singh, B. Alternative treatment strategies for neuropathic pain: role of Indian medicinal plants and compounds of plant origin-A review. Biomed Pharmacother 2017;92:634–50. https://doi.org/10.1016/j.biopha.2017.05.079.
Garg, G, Adams, JD. Treatment of neuropathic pain with plant medicines. Chin J Integr Med 2012;18:565–70. https://doi.org/10.1007/s11655-012-1188-6.
Lin, YL, Chang, HC, Chen, TL, Chang, JH, Chiu, WT, Lin, JW, et al.. Resveratrol protects against oxidized LDL-induced breakage of the blood-brain barrier by lessening disruption of tight junctions and apoptotic insults to mouse cerebrovascular endothelial cells. J Nutr 2010;140:2187–92. https://doi.org/10.3945/jn.110.123505.
Rege, SD, Geetha, T, Griffin, GD, Broderick, TL, Babu, JR. Neuroprotective effects of resveratrol in Alzheimer disease pathology. Front Aging Neurosci 2014;6:218. https://doi.org/10.3389/fnagi.2014.00218.
Sönmez, U, Sönmez, A, Erbil, G, Tekmen, I, Baykara, B. Neuroprotective effects of resveratrol against traumatic brain injury in immature rats. Neurosci Lett 2007;420:133–7. https://doi.org/10.1016/j.neulet.2007.04.070.
Zhang, Y, Li, Y, Wang, Y, Wang, G, Mao, L, Zhang, D, et al.. Effects of resveratrol on learning and memory in rats with vascular dementia. Mol Med Rep 2019;20:4587–93. https://doi.org/10.3892/mmr.2019.10723.
Herzberg, D, Strobel, P, Chihuailaf, R, Ramirez-Reveco, A, Müller, H, Werner, M, et al.. Spinal reactive oxygen species and oxidative damage mediate chronic pain in lame dairy cows. Animals 2019;9:693. https://doi.org/10.3390/ani9090693.
Ma, XR, Sun, Z, Han, X, Li, S, Jiang, X, Chen, S, et al.. Neuroprotective effect of resveratrol via activation of Sirt1 signaling in a rat model of combined diabetes and alzheimer’s disease. Front Neurosci 2020;13:1400. https://doi.org/10.3389/fnins.2019.01400.
Carrasco, C, Naziroǧlu, M, Rodríguez, AB, Pariente, JA. Neuropathic pain: delving into the oxidative origin and the possible implication of transient receptor potential channels. Front Physiol 2018;9:95. https://doi.org/10.3389/fphys.2018.00095.
Ma, X, Sun, Z, Liu, Y, Jia, Y, Zhang, B, Zhang, J. Resveratrol improves cognition and reduces oxidative stress in rats with vascular dementia. Neural Regen Res 2013;8:2050–59. https://doi.org/10.3969/j.issn.1673-5374.2013.22.004.
Ghowsi, M, Khazali, H, Sisakhtnezhad, S. The effect of resveratrol on oxidative stress in the liver and serum of a rat model of polycystic ovary syndrome: an experimental study. IJRM 2018;16:149–58. https://doi.org/10.29252/ijrm.16.3.149.
Hertz, L, Lovatt, D, Goldman, SA, Nedergaard, M. Adrenoceptors in brain: cellular gene expression and effects on astrocytic metabolism and [Ca2+]i. Neurochem Int 2010;57:411–20. https://doi.org/10.1016/j.neuint.2010.03.019.
Kukushkin, ML, Smirnova, VS, Gorizontova, MP, Mironova, IV, Zinkevich, VA. Effect of clofelin and propranolol on the development of neurogenic pain syndrome in rats. Patol Fiziol Eksp Ter 1993:16–9.
Galgut, JM. Activation of adrenergic receptors by resveratrol elicits pigment aggregation in isolated melanophores of adult toad, Bufo melanostictus leading to skin lightening. Biosci Biotech Res Comm 2015;8:98–103.
Chaplan, SR, Bach, FW, Pogrel, JW, Chung, JM, Yaksh, TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods 1994;53:55–63. https://doi.org/10.1016/0165-0270(94)90144-9.
Xu, Y, Lin, D, Yu, X, Xie, X, Wang, L, Lian, L, et al.. The antinociceptive effects of ferulic acid on neuropathic pain: involvement of descending monoaminergic system and opioid receptors. Oncotarget 2016;7:20455–68. https://doi.org/10.18632/oncotarget.7973.
Martin, LJ, Piltonen, MH, Gauthier, J, Convertino, M, Acland, EL, Dokholyan, NV, et al.. Differences in the antinociceptive effects and binding properties of propranolol and bupranolol enantiomers. J Pain 2015;16:1321–33. https://doi.org/10.1016/j.jpain.2015.09.004.
Yücel, NT, Can, OD, Özkay, UD. Catecholaminergic and opioidergic system mediated effects of reboxetine on diabetic neuropathic pain. Psychopharmacology 2020;237:1131–45.

Auteurs

Mohammad Ali Zabihian (MA)

Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Mehdi Hosseini (M)

Student Research Committee, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Farideh Bahrami (F)

Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Maryam Iman (M)

Department of Pharmaceutics, Faculty of Pharmacy, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Maedeh Ghasemi (M)

Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Mohammad Taghi Mohammadi (MT)

Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

Zahra Bahari (Z)

Department of Physiology and Medical Physics, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.

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