Skip to main content
Top
Published in: Chinese Medicine 1/2021

Open Access 01-12-2021 | Alkaloids | Research

Corydalis saxicola Bunting total alkaloids attenuate paclitaxel-induced peripheral neuropathy through PKCε/p38 MAPK/TRPV1 signaling pathway

Authors: Chu Xue, Si-Xue Liu, Jie Hu, Jin Huang, Hong-Min Liu, Zhi-Xia Qiu, Fang Huang

Published in: Chinese Medicine | Issue 1/2021

Login to get access

Abstract

Background

Corydalis saxicola Bunting, affiliated with the Papaveraceae Juss., has been proven to work well in anti-inflammation, hemostasis, and analgesia. This study was designed to observe the effect and potential mechanism of Corydalis saxicola Bunting total alkaloids (CSBTA) on paclitaxel-induced peripheral neuropathy (PIPN).

Materials and methods

Rats were injected 2 mg/kg paclitaxel 4 times and administrated with 30 or 120 mg/kg CSBTA. Mechanical and thermal allodynia and hyperalgesia were tested. After 40 days, serum was collected to detect PGE2, TNF-α, and IL-1β by ELISA. The L4-L6 segment spinal cord, DRG, and plantar skin were harvested, and Western-blot or RT-qPCR analyzed protein and gene levels of pro-inflammatory cytokines, p38 MAPK, PKCε, and TRPV1. The PIPN cell model was established with paclitaxel (300 nM, 5 d) in primary DRG neurons. We examined the effect of CSBTA (25 μg/ml or 50 μg/ml) by measuring the mRNA levels in PGE2, TNF-α and CGRP, and the protein expression on the PKCε/p38 MAPK/TRPV1 signaling pathway in the PIPN cell model.

Results

The results showed that CSBTA effectively ameliorated allodynia and hyperalgesia, and regulated cytokines' contents (PGE2, TNF-α, and IL-1β) and neuropeptides (CGRP and SP) in different tissues in vivo. In addition, CSBTA significantly decreased cytokine gene levels of DRG neurons (PGE2, TNF-α, and CGRP) and the protein expressions of PKCε/p38 MAPK/TRPV1 signaling pathway in vivo and in vitro.

Conclusion

Therefore, CSBTA has a perspective therapeutic effect on the treatment of paclitaxel-induced peripheral neuropathy.
Literature
1.
go back to reference Duggett NA, Griffiths LA, Flatters SJL. Paclitaxel-induced painful neuropathy is associated with changes in mitochondrial bioenergetics, glycolysis and an energy deficit in dorsal root ganglia neurons. Pain. 2017;158(8):1499–508.PubMedPubMedCentralCrossRef Duggett NA, Griffiths LA, Flatters SJL. Paclitaxel-induced painful neuropathy is associated with changes in mitochondrial bioenergetics, glycolysis and an energy deficit in dorsal root ganglia neurons. Pain. 2017;158(8):1499–508.PubMedPubMedCentralCrossRef
2.
go back to reference Zhang H, Boyette-Davis JA, Kosturakis AK, Li Y, Yoon SY, Walters ET. Induction of monocyte chemoattractant protein-1 (MCP-1) and its receptor CCR2 in primary sensory neurons contributes to paclitaxel-induced peripheral neuropathy. J PAIN. 2013;14(10):1031–44.PubMedPubMedCentralCrossRef Zhang H, Boyette-Davis JA, Kosturakis AK, Li Y, Yoon SY, Walters ET. Induction of monocyte chemoattractant protein-1 (MCP-1) and its receptor CCR2 in primary sensory neurons contributes to paclitaxel-induced peripheral neuropathy. J PAIN. 2013;14(10):1031–44.PubMedPubMedCentralCrossRef
3.
go back to reference Xie JD, Chen SR, Pan HL. Presynaptic N-Methyl-d-aspartate (NMDA) receptor activity is increased through protein kinase C in paclitaxel-induced neuropathic pain. J Biol Chem. 2016;291(37):19364–73.PubMedCrossRef Xie JD, Chen SR, Pan HL. Presynaptic N-Methyl-d-aspartate (NMDA) receptor activity is increased through protein kinase C in paclitaxel-induced neuropathic pain. J Biol Chem. 2016;291(37):19364–73.PubMedCrossRef
4.
go back to reference Sisignano M, Baron R, Scholich K, Geisslinger G. Mechanism-based treatment for chemotherapy-induced peripheral neuropathic pain. Nat Rev Neurol. 2014;10(12):694–707.PubMedCrossRef Sisignano M, Baron R, Scholich K, Geisslinger G. Mechanism-based treatment for chemotherapy-induced peripheral neuropathic pain. Nat Rev Neurol. 2014;10(12):694–707.PubMedCrossRef
5.
go back to reference Ba XY, Wang JL, Zhou SY, Luo XX, Peng Y, Yang SM, Hao Y, Jin GY. Cinobufacini protects against paclitaxel-induced peripheral neuropathic pain and suppresses TRPV1 up-regulation and spinal astrocyte activation in rats. Biomed Pharmacother. 2018;108:76–84.PubMedCrossRef Ba XY, Wang JL, Zhou SY, Luo XX, Peng Y, Yang SM, Hao Y, Jin GY. Cinobufacini protects against paclitaxel-induced peripheral neuropathic pain and suppresses TRPV1 up-regulation and spinal astrocyte activation in rats. Biomed Pharmacother. 2018;108:76–84.PubMedCrossRef
6.
go back to reference Chen Y, Yang C, Wang ZJ. Proteinase-activated receptor 2 sensitizes transient receptor potential vanilloid 1, transient receptor potential vanilloid 4, and transient receptor potential ankyrin 1 in paclitaxel-induced neuropathic pain. Neuroscience. 2011;193:440–51.PubMedCrossRef Chen Y, Yang C, Wang ZJ. Proteinase-activated receptor 2 sensitizes transient receptor potential vanilloid 1, transient receptor potential vanilloid 4, and transient receptor potential ankyrin 1 in paclitaxel-induced neuropathic pain. Neuroscience. 2011;193:440–51.PubMedCrossRef
7.
go back to reference Hara T, Chiba T, Abe K, Makabe A, Ikeno S, Kawakam K. Effect of paclitaxel on transient receptor potential vanilloid 1 in rat dorsal root ganglion. Pain. 2013;154(6):882–9.PubMedCrossRef Hara T, Chiba T, Abe K, Makabe A, Ikeno S, Kawakam K. Effect of paclitaxel on transient receptor potential vanilloid 1 in rat dorsal root ganglion. Pain. 2013;154(6):882–9.PubMedCrossRef
8.
go back to reference Li Y, Adamek P, Zhang H, Tatsui CE, Rhines LD, Mrozkova P, Dougherty PM. The cancer chemotherapeutic paclitaxel increases human and rodent sensory neuron responses to TRPV1 by activation of TLR4. J Neurosci. 2015;35(39):13487–500.PubMedPubMedCentralCrossRef Li Y, Adamek P, Zhang H, Tatsui CE, Rhines LD, Mrozkova P, Dougherty PM. The cancer chemotherapeutic paclitaxel increases human and rodent sensory neuron responses to TRPV1 by activation of TLR4. J Neurosci. 2015;35(39):13487–500.PubMedPubMedCentralCrossRef
10.
go back to reference Szallasi A, Sheta M. Targeting TRPV1 for pain relief: limits, losers and laurels. Expert Opin Investig Drugs. 2012;21(9):1351–69.PubMedCrossRef Szallasi A, Sheta M. Targeting TRPV1 for pain relief: limits, losers and laurels. Expert Opin Investig Drugs. 2012;21(9):1351–69.PubMedCrossRef
11.
go back to reference Szolcsányi J, Pintér E. Transient receptor potential vanilloid 1 as a therapeutic target in analgesia. Expert Opin Ther Targets. 2013;17(6):641–57.PubMedCrossRef Szolcsányi J, Pintér E. Transient receptor potential vanilloid 1 as a therapeutic target in analgesia. Expert Opin Ther Targets. 2013;17(6):641–57.PubMedCrossRef
12.
go back to reference Quartu M, Carozzi VA, Dorsey SG, Serra MP, Marmiroli P. Bortezomib treatment produces nocifensive behavior and changes in the expression of TRPV1, CGRP, and substance P in the Rat DRG, spinal cord, and sciatic nerve. Biomed Res Int. 2014;14:180428. Quartu M, Carozzi VA, Dorsey SG, Serra MP, Marmiroli P. Bortezomib treatment produces nocifensive behavior and changes in the expression of TRPV1, CGRP, and substance P in the Rat DRG, spinal cord, and sciatic nerve. Biomed Res Int. 2014;14:180428.
13.
go back to reference Kee KH, Seon-Hee H, Salahadin A. Tempol ameliorates and prevents mechanical hyperalgesia in a rat model of chemotherapy-induced neuropathic pain. Front Pharmacol. 2017;7:532. Kee KH, Seon-Hee H, Salahadin A. Tempol ameliorates and prevents mechanical hyperalgesia in a rat model of chemotherapy-induced neuropathic pain. Front Pharmacol. 2017;7:532.
14.
15.
go back to reference Schönwasser DC, Marais RM, Marshall CJ, et al. Activation of p38 MAPK in primary afferent neurons kinase/extracellular signal-regulated kinase pathway by conventional, novel, and atypical protein kinase C isotypes. Mol Cell Biol. 1998;18(2):790–801.PubMedPubMedCentralCrossRef Schönwasser DC, Marais RM, Marshall CJ, et al. Activation of p38 MAPK in primary afferent neurons kinase/extracellular signal-regulated kinase pathway by conventional, novel, and atypical protein kinase C isotypes. Mol Cell Biol. 1998;18(2):790–801.PubMedPubMedCentralCrossRef
16.
go back to reference Ji RR, Samad TA, Jin SX, Schmoll R, Wool CJ. p38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia. Neuron. 2002;36(1):57–68.PubMedCrossRef Ji RR, Samad TA, Jin SX, Schmoll R, Wool CJ. p38 MAPK activation by NGF in primary sensory neurons after inflammation increases TRPV1 levels and maintains heat hyperalgesia. Neuron. 2002;36(1):57–68.PubMedCrossRef
17.
go back to reference Asih PR, Prikas E, Stefanoska K, et al. Functions of p38 MAP kinases in the central nervous system. Front Mol Neurosci. 2020;8(13):570586.CrossRef Asih PR, Prikas E, Stefanoska K, et al. Functions of p38 MAP kinases in the central nervous system. Front Mol Neurosci. 2020;8(13):570586.CrossRef
18.
19.
go back to reference Itoh Y, Sendo T, Hirakawa T, et al. Pemirolast potently attenuates paclitaxel hypersensitivity reactions through inhibition of the release of sensory neuropeptides in rats. Neuropharmacology. 2004;46(6):888–94.PubMedCrossRef Itoh Y, Sendo T, Hirakawa T, et al. Pemirolast potently attenuates paclitaxel hypersensitivity reactions through inhibition of the release of sensory neuropeptides in rats. Neuropharmacology. 2004;46(6):888–94.PubMedCrossRef
20.
go back to reference Li Y, Zhang HM, et al. MAPK signaling downstream to TLR4 contributes to paclitaxel-induced peripheral neuropathy. Brain Behav Immun. 2015;49:S0889159115001543.CrossRef Li Y, Zhang HM, et al. MAPK signaling downstream to TLR4 contributes to paclitaxel-induced peripheral neuropathy. Brain Behav Immun. 2015;49:S0889159115001543.CrossRef
21.
go back to reference Numazaki M, Tominaga T, Toyooka H, Tominaga M. Direct phosphorylation of capsaicin receptor VR1 by protein kinase Cε and identification of two target serine residues. J Biol Chem. 2002;277(16):13375–8.PubMedCrossRef Numazaki M, Tominaga T, Toyooka H, Tominaga M. Direct phosphorylation of capsaicin receptor VR1 by protein kinase Cε and identification of two target serine residues. J Biol Chem. 2002;277(16):13375–8.PubMedCrossRef
22.
go back to reference Yu JJ, Liu QY, Lu XY, Li XN, Li N, Liu BL, Huang F, Qiu ZX. Inhibitory and inductive effects of Corydalis saxicola Bunting total alkaloids (CSBTA) on cytochrome P450s in rats. Phytother Res. 2018;32(9):1818–27.PubMedCrossRef Yu JJ, Liu QY, Lu XY, Li XN, Li N, Liu BL, Huang F, Qiu ZX. Inhibitory and inductive effects of Corydalis saxicola Bunting total alkaloids (CSBTA) on cytochrome P450s in rats. Phytother Res. 2018;32(9):1818–27.PubMedCrossRef
23.
go back to reference Wu Y, Lu TL, Ji D, Zhou Y, Mao CQ. Isolation and structural identification of alkaloids from Corydalis saxicola. J Nanjing Univ TCM. 2015;1:81–3. Wu Y, Lu TL, Ji D, Zhou Y, Mao CQ. Isolation and structural identification of alkaloids from Corydalis saxicola. J Nanjing Univ TCM. 2015;1:81–3.
24.
go back to reference Cheng XX, Wang DM, Jiang L, Yang D. Simultaneous determination of eight bioactive alkaloids in Corydalis saxicola by high-performance liquid chromatography coupled with diode array detection. Phytochem Anal. 2008;19(5):420–8.PubMedCrossRef Cheng XX, Wang DM, Jiang L, Yang D. Simultaneous determination of eight bioactive alkaloids in Corydalis saxicola by high-performance liquid chromatography coupled with diode array detection. Phytochem Anal. 2008;19(5):420–8.PubMedCrossRef
25.
go back to reference Kuai CP, JuL J, Hu PP, Huang F. Corydalis saxicola alkaloids attenuate cisplatin-induced neuropathic pain by reducing loss of IENF and blocking TRPV1 activation. Am J Chin Med. 2020;48(2):407–28.PubMedCrossRef Kuai CP, JuL J, Hu PP, Huang F. Corydalis saxicola alkaloids attenuate cisplatin-induced neuropathic pain by reducing loss of IENF and blocking TRPV1 activation. Am J Chin Med. 2020;48(2):407–28.PubMedCrossRef
26.
go back to reference Ju LJ, Hu PP, Chen P, Wu JJ, Li ZQ, Qiu ZX, Cheng J, Huang F. Corydalis saxicola Bunting total alkaloids attenuate Walker 256-induced bone pain and osteoclastogenesis by suppressing RANKL-induced NF-κB and c-Fos/NFATc1 pathways in rats. Front Pharmacol. 2021;26(11):609119.CrossRef Ju LJ, Hu PP, Chen P, Wu JJ, Li ZQ, Qiu ZX, Cheng J, Huang F. Corydalis saxicola Bunting total alkaloids attenuate Walker 256-induced bone pain and osteoclastogenesis by suppressing RANKL-induced NF-κB and c-Fos/NFATc1 pathways in rats. Front Pharmacol. 2021;26(11):609119.CrossRef
27.
go back to reference Gao W, Zan Y, Wang ZJ, Hu XY, Huang F. Quercetin ameliorates paclitaxel-induced neuropathic pain by stabilizing mast cells, and subsequently blocking PKCε-dependent activation of TRPV1. Acta Pharmacol Sin. 2016;37(9):1166–77.PubMedPubMedCentralCrossRef Gao W, Zan Y, Wang ZJ, Hu XY, Huang F. Quercetin ameliorates paclitaxel-induced neuropathic pain by stabilizing mast cells, and subsequently blocking PKCε-dependent activation of TRPV1. Acta Pharmacol Sin. 2016;37(9):1166–77.PubMedPubMedCentralCrossRef
28.
go back to reference Li YY, Yin CY, Li XJ. Electroacupuncture alleviates paclitaxel-induced peripheral neuropathic pain in rats via suppressing TLR4 signaling and TRPV1 upregulation in sensory neurons. Int J Mol Sci. 2019;20(23):5917.PubMedCentralCrossRef Li YY, Yin CY, Li XJ. Electroacupuncture alleviates paclitaxel-induced peripheral neuropathic pain in rats via suppressing TLR4 signaling and TRPV1 upregulation in sensory neurons. Int J Mol Sci. 2019;20(23):5917.PubMedCentralCrossRef
29.
go back to reference Nataliia K, Mickael D, Dita S-K. Losartan attenuates neuroinflammation and neuropathic pain in paclitaxel-induced peripheral neuropathy. J Cell Mol Med. 2020;24(14):7949–58.CrossRef Nataliia K, Mickael D, Dita S-K. Losartan attenuates neuroinflammation and neuropathic pain in paclitaxel-induced peripheral neuropathy. J Cell Mol Med. 2020;24(14):7949–58.CrossRef
30.
go back to reference Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods. 1994;53(1):55–63.PubMedCrossRef Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods. 1994;53(1):55–63.PubMedCrossRef
31.
go back to reference Brenner DS, Golden JP, Vogt SK. A simple and inexpensive method for determining cold sensitivity and adaptation in mice. J Vis Exp. 2015;17(97):52640. Brenner DS, Golden JP, Vogt SK. A simple and inexpensive method for determining cold sensitivity and adaptation in mice. J Vis Exp. 2015;17(97):52640.
32.
go back to reference Hu PP, Huang F. Yunnan Baiyao ameliorates MIA-induced knee osteoarthritis pain in rats through anti-inflammatory effect. Chin J Clin Pharm Therap. 2019;3:254–9. Hu PP, Huang F. Yunnan Baiyao ameliorates MIA-induced knee osteoarthritis pain in rats through anti-inflammatory effect. Chin J Clin Pharm Therap. 2019;3:254–9.
33.
34.
go back to reference Zhou FQ. Genetic study of axon regeneration with cultured adult dorsal root Ganglion Neurons. J Vis Exp. 2012;66:e4141. Zhou FQ. Genetic study of axon regeneration with cultured adult dorsal root Ganglion Neurons. J Vis Exp. 2012;66:e4141.
35.
go back to reference Zhu JC, Li Y, Liang JH, Li JX, Huang K, Li J, Liu CY. The neuroprotective effect of oxytocin on vincristine-induced neurotoxicity in mice. Toxicol Lett. 2021;340:67–76.PubMedCrossRef Zhu JC, Li Y, Liang JH, Li JX, Huang K, Li J, Liu CY. The neuroprotective effect of oxytocin on vincristine-induced neurotoxicity in mice. Toxicol Lett. 2021;340:67–76.PubMedCrossRef
36.
go back to reference Qiu ZX, Dong JJ, Xue C, Li XN, Liu K, Liu BL, Cheng J, Huang F. Liuwei Dihuang pills alleviate the polycystic ovary syndrome with improved insulin sensitivity through PI3K/Akt signaling pathway. J Ethnopharmacol. 2020;250:111965.PubMedCrossRef Qiu ZX, Dong JJ, Xue C, Li XN, Liu K, Liu BL, Cheng J, Huang F. Liuwei Dihuang pills alleviate the polycystic ovary syndrome with improved insulin sensitivity through PI3K/Akt signaling pathway. J Ethnopharmacol. 2020;250:111965.PubMedCrossRef
37.
go back to reference Myers RR, Campana WM, Shubayev VI. The role of neuroinflammation in neuropathic pain: mechanisms and therapeutic targets. Drug Discov Today. 2006;11(1–2):8–20.PubMedCrossRef Myers RR, Campana WM, Shubayev VI. The role of neuroinflammation in neuropathic pain: mechanisms and therapeutic targets. Drug Discov Today. 2006;11(1–2):8–20.PubMedCrossRef
38.
go back to reference Ma W, Eisenach JC. Intraplantar injection of a cyclooxygenase inhibitor ketorolac reduces immunoreactivities of substance p, calcitonin gene-related peptide, and dynorphin in the dorsal horn of rats with nerve injury or inflammation. Neuroscience. 2003;121(3):681–90.PubMedCrossRef Ma W, Eisenach JC. Intraplantar injection of a cyclooxygenase inhibitor ketorolac reduces immunoreactivities of substance p, calcitonin gene-related peptide, and dynorphin in the dorsal horn of rats with nerve injury or inflammation. Neuroscience. 2003;121(3):681–90.PubMedCrossRef
39.
go back to reference Chiba T, Oka Y, Kambe T, Koizumi N, Abe K, Kawakami K, Utsunomiya I, Taguchi K. Paclitaxel-induced peripheral neuropathy increases substance P release in rat spinal cord. Eur J Pharmacol. 2016;770:46–51.PubMedCrossRef Chiba T, Oka Y, Kambe T, Koizumi N, Abe K, Kawakami K, Utsunomiya I, Taguchi K. Paclitaxel-induced peripheral neuropathy increases substance P release in rat spinal cord. Eur J Pharmacol. 2016;770:46–51.PubMedCrossRef
40.
go back to reference Jia M, Wu C, Gao F. Activation of NLRP3 inflammasome in peripheral nerve contributes to paclitaxel-induced neuropathic pain. Mol Pain. 2017;13:1744806917719804.PubMedCrossRef Jia M, Wu C, Gao F. Activation of NLRP3 inflammasome in peripheral nerve contributes to paclitaxel-induced neuropathic pain. Mol Pain. 2017;13:1744806917719804.PubMedCrossRef
41.
go back to reference Sałat K, Cios A, Wyska E. Antiallodynic and antihyperalgesic activity of 3-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-dihydrofuran-2-one compared to pregabalin in chemotherapy-induced neuropathic pain in mice. Pharmacol Biochem Behav. 2014;122:173–81.PubMedCrossRef Sałat K, Cios A, Wyska E. Antiallodynic and antihyperalgesic activity of 3-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-dihydrofuran-2-one compared to pregabalin in chemotherapy-induced neuropathic pain in mice. Pharmacol Biochem Behav. 2014;122:173–81.PubMedCrossRef
42.
go back to reference Vissers K, Meert T. A behavioral and pharmacological validation of the acetone spray test in gerbils with a chronic constriction injury. Anesth Analg. 2005;101(2):457–64.PubMedCrossRef Vissers K, Meert T. A behavioral and pharmacological validation of the acetone spray test in gerbils with a chronic constriction injury. Anesth Analg. 2005;101(2):457–64.PubMedCrossRef
43.
go back to reference Wang Y, Gao Y, Tian Q, Deng Q, Wang Y, Zhou T. TRPV1 SUMOylation regulates nociceptive signaling in models of inflammatory pain. Nat Commun. 2018;9(1):1529–35.PubMedPubMedCentralCrossRef Wang Y, Gao Y, Tian Q, Deng Q, Wang Y, Zhou T. TRPV1 SUMOylation regulates nociceptive signaling in models of inflammatory pain. Nat Commun. 2018;9(1):1529–35.PubMedPubMedCentralCrossRef
44.
go back to reference Caterina MJ. Impaired nociception and pain sensation in mice lacking the Capsaicin Receptor. Science. 2000;288(5464):306–13.PubMedCrossRef Caterina MJ. Impaired nociception and pain sensation in mice lacking the Capsaicin Receptor. Science. 2000;288(5464):306–13.PubMedCrossRef
45.
go back to reference He Y, Wang ZJ. Nociceptor Beta II, Delta, and Epsilon isoforms of PKC differentially mediate paclitaxel-induced spontaneous and evoked pain. J Neurosci. 2015;35(11):4614–25.PubMedPubMedCentralCrossRef He Y, Wang ZJ. Nociceptor Beta II, Delta, and Epsilon isoforms of PKC differentially mediate paclitaxel-induced spontaneous and evoked pain. J Neurosci. 2015;35(11):4614–25.PubMedPubMedCentralCrossRef
46.
go back to reference Dougherty PM, Cata JP, Cordella JV, Burton A, Weng HR. Taxol induced sensory disturbances characterized by preferential impairment of myelinated fiber function in cancer patients. Pain. 2004;109(1–2):132–42.PubMedCrossRef Dougherty PM, Cata JP, Cordella JV, Burton A, Weng HR. Taxol induced sensory disturbances characterized by preferential impairment of myelinated fiber function in cancer patients. Pain. 2004;109(1–2):132–42.PubMedCrossRef
47.
go back to reference Blaker AL, Mitchell CM, Semple EA. Identifying the role of novel protein kinase C isoforms in mediating paclitaxel-induced peripheral neuropathy. J Neurosci. 2015;35(28):10101–12.PubMedPubMedCentralCrossRef Blaker AL, Mitchell CM, Semple EA. Identifying the role of novel protein kinase C isoforms in mediating paclitaxel-induced peripheral neuropathy. J Neurosci. 2015;35(28):10101–12.PubMedPubMedCentralCrossRef
48.
go back to reference Yamamoto H, Kawamata T, Ninomiya T, Omote K, Namiki A. Endothelin-1 enhances capsaicin-evoked intracellular Ca2+ response via activation of endothelin a receptor in a protein kinase Cε -dependent manner in dorsal root ganglion neurons. Neuroscience. 2006;137(3):949–60.PubMedCrossRef Yamamoto H, Kawamata T, Ninomiya T, Omote K, Namiki A. Endothelin-1 enhances capsaicin-evoked intracellular Ca2+ response via activation of endothelin a receptor in a protein kinase Cε -dependent manner in dorsal root ganglion neurons. Neuroscience. 2006;137(3):949–60.PubMedCrossRef
49.
go back to reference Khasar SG, Lin YH, Martin A, Dadgar J, McMahon T, Dan W. A novel nociceptor signaling pathway revealed in protein kinase C ε mutant mice. Neuron. 1999;24(1):253–60.PubMedCrossRef Khasar SG, Lin YH, Martin A, Dadgar J, McMahon T, Dan W. A novel nociceptor signaling pathway revealed in protein kinase C ε mutant mice. Neuron. 1999;24(1):253–60.PubMedCrossRef
50.
go back to reference Hucho TB, Dina OA, Kuhn J, Levine JD. Estrogen controls PKCε dependent mechanical hyperalgesia through direct action on nociceptive neurons. Eur J Neurosci. 2006;24(2):527–34.PubMedCrossRef Hucho TB, Dina OA, Kuhn J, Levine JD. Estrogen controls PKCε dependent mechanical hyperalgesia through direct action on nociceptive neurons. Eur J Neurosci. 2006;24(2):527–34.PubMedCrossRef
51.
53.
go back to reference Honda K, Shinoda M, Kondo M, et al. Sensitization of TRPV1 and TRPA1 via peripheral mGluR5 signaling contributes to thermal and mechanical hypersensitivity. Pain. 2017;1:1754–64.CrossRef Honda K, Shinoda M, Kondo M, et al. Sensitization of TRPV1 and TRPA1 via peripheral mGluR5 signaling contributes to thermal and mechanical hypersensitivity. Pain. 2017;1:1754–64.CrossRef
54.
go back to reference Sikand P, Premkumar LS. Potentiation of glutamatergic synaptic transmission by protein kinase C-mediated sensitization of TRPV1 at the first sensory synapse. J Physiol. 2007;581(2):631–47.PubMedPubMedCentralCrossRef Sikand P, Premkumar LS. Potentiation of glutamatergic synaptic transmission by protein kinase C-mediated sensitization of TRPV1 at the first sensory synapse. J Physiol. 2007;581(2):631–47.PubMedPubMedCentralCrossRef
55.
go back to reference Schäfers M, Svensson CI, Sommer C, et al. Tumor necrosis factor-alpha induces mechanical allodynia after spinal nerve ligation by activation of p38 MAPK in primary sensory neurons. J Neurosci. 2003;23(7):2517–21.PubMedPubMedCentralCrossRef Schäfers M, Svensson CI, Sommer C, et al. Tumor necrosis factor-alpha induces mechanical allodynia after spinal nerve ligation by activation of p38 MAPK in primary sensory neurons. J Neurosci. 2003;23(7):2517–21.PubMedPubMedCentralCrossRef
56.
go back to reference Svensson CI, Marsala M, Westerlund A, et al. Activation of p38 mitogen-activated protein kinase in spinal microglia is a critical link in inflammation-induced spinal pain processing. J Neurochem. 2003;86(6):1534–44.PubMedCrossRef Svensson CI, Marsala M, Westerlund A, et al. Activation of p38 mitogen-activated protein kinase in spinal microglia is a critical link in inflammation-induced spinal pain processing. J Neurochem. 2003;86(6):1534–44.PubMedCrossRef
57.
go back to reference Chaumette T, Delay L, Barbier J, et al. c-Jun/p38MAPK/ASIC3 pathways specifically activated by nerve growth factor through TrkA are crucial for mechanical allodynia development. Pain. 2020;161(5):1109–23.PubMedCrossRef Chaumette T, Delay L, Barbier J, et al. c-Jun/p38MAPK/ASIC3 pathways specifically activated by nerve growth factor through TrkA are crucial for mechanical allodynia development. Pain. 2020;161(5):1109–23.PubMedCrossRef
58.
go back to reference Facer P, Casula MA, Smith GD, et al. Differential expression of the capsaicin receptor TRPV1 and related novel receptors TRPV3, TRPV4 and TRPM8 in normal human tissues and changes in traumatic and diabetic neuropathy. BMC Neurol. 2007;23(7):11.CrossRef Facer P, Casula MA, Smith GD, et al. Differential expression of the capsaicin receptor TRPV1 and related novel receptors TRPV3, TRPV4 and TRPM8 in normal human tissues and changes in traumatic and diabetic neuropathy. BMC Neurol. 2007;23(7):11.CrossRef
59.
go back to reference Sun L, Li H, Tai LW, et al. Adiponectin regulates thermal nociception in a mouse model of neuropathic pain. Br J Anaesth. 2018;120(6):1356–67.PubMedCrossRef Sun L, Li H, Tai LW, et al. Adiponectin regulates thermal nociception in a mouse model of neuropathic pain. Br J Anaesth. 2018;120(6):1356–67.PubMedCrossRef
60.
go back to reference Amantini C, Mosca M, Nabissi M, et al. Capsaicin-induced apoptosis of glioma cells is mediated by TRPV1 vanilloid receptor and requires p38 MAPK activation. J Neurochem. 2007;102(3):977–90.PubMedCrossRef Amantini C, Mosca M, Nabissi M, et al. Capsaicin-induced apoptosis of glioma cells is mediated by TRPV1 vanilloid receptor and requires p38 MAPK activation. J Neurochem. 2007;102(3):977–90.PubMedCrossRef
61.
go back to reference Miyagawa YI, Kobayashi K, Yamanaka H, et al. Peripherally increased artemin is a key regulator of TRPA1/V1 expression in primary afferent neurons. Mol Pain. 2015;8(11):8. Miyagawa YI, Kobayashi K, Yamanaka H, et al. Peripherally increased artemin is a key regulator of TRPA1/V1 expression in primary afferent neurons. Mol Pain. 2015;8(11):8.
62.
go back to reference Nishida T, Tsubota M, Kawaishi Y, Yamanishi H, Kamitani N, Sekiguchi F, Ishikura H, Liu K, Nishibori M, Kawabata A. Involvement of high mobility group box 1 in the development and maintenance of chemotherapy-induced peripheral neuropathy in rats. Toxicology. 2016;365:48–58.PubMedCrossRef Nishida T, Tsubota M, Kawaishi Y, Yamanishi H, Kamitani N, Sekiguchi F, Ishikura H, Liu K, Nishibori M, Kawabata A. Involvement of high mobility group box 1 in the development and maintenance of chemotherapy-induced peripheral neuropathy in rats. Toxicology. 2016;365:48–58.PubMedCrossRef
63.
go back to reference Lees JG, Makker PGS, Tonkin RS. Immune-mediated processes implicated in chemotherapy-induced peripheral neuropathy. Eur J Cancer. 2017;73:22–9.PubMedCrossRef Lees JG, Makker PGS, Tonkin RS. Immune-mediated processes implicated in chemotherapy-induced peripheral neuropathy. Eur J Cancer. 2017;73:22–9.PubMedCrossRef
64.
go back to reference Hana S, Irina V. Pathophysiology of chemotherapy-induced peripheral neuropathy. Front Mol Neurosci. 2017;10:174.CrossRef Hana S, Irina V. Pathophysiology of chemotherapy-induced peripheral neuropathy. Front Mol Neurosci. 2017;10:174.CrossRef
65.
go back to reference Wu GJ, Wang ZX, Shan PR, et al. Suppression of Netrin-1 attenuates angiotension II-induced cardiac remodeling through the PKC/MAPK signaling pathway. Biomed Pharmacother. 2020;130:110495.PubMedCrossRef Wu GJ, Wang ZX, Shan PR, et al. Suppression of Netrin-1 attenuates angiotension II-induced cardiac remodeling through the PKC/MAPK signaling pathway. Biomed Pharmacother. 2020;130:110495.PubMedCrossRef
66.
go back to reference Mamilla RC, Amrita K, Sujatha S, et al. Oral administration of eugenol oleate cures experimental visceral leishmaniasis through cytokines abundance. Cytokine. 2021;145:155301.CrossRef Mamilla RC, Amrita K, Sujatha S, et al. Oral administration of eugenol oleate cures experimental visceral leishmaniasis through cytokines abundance. Cytokine. 2021;145:155301.CrossRef
67.
go back to reference Pu YW, Liu ZJ, Tian H, et al. The immunomodulatory effect of Poria cocos polysaccharides is mediated by the Ca2+/PKC/p38/NF-κB signaling pathway in macrophages. Int Immunopharmacol. 2019;72:252–7.PubMedCrossRef Pu YW, Liu ZJ, Tian H, et al. The immunomodulatory effect of Poria cocos polysaccharides is mediated by the Ca2+/PKC/p38/NF-κB signaling pathway in macrophages. Int Immunopharmacol. 2019;72:252–7.PubMedCrossRef
68.
go back to reference Xu BY, Tang XD, Chen J, et al. Rifampicin induces clathrin-dependent endocytosis and ubiquitin–proteasome degradation of MRP2 via oxidative stress-activated PKC-ERK/JNK/p38 and PI3K signaling pathways in HepG2 cells. Acta Pharmacol Sin. 2020;41(1):56–64.PubMedCrossRef Xu BY, Tang XD, Chen J, et al. Rifampicin induces clathrin-dependent endocytosis and ubiquitin–proteasome degradation of MRP2 via oxidative stress-activated PKC-ERK/JNK/p38 and PI3K signaling pathways in HepG2 cells. Acta Pharmacol Sin. 2020;41(1):56–64.PubMedCrossRef
69.
go back to reference Sun L, Wang GD, He MF, et al. Effect and mechanism of the CACNA2D1-CGRP pathway in osteoarthritisinduced ongoing pain. Biomed Pharmacother. 2020;129:110374.PubMedCrossRef Sun L, Wang GD, He MF, et al. Effect and mechanism of the CACNA2D1-CGRP pathway in osteoarthritisinduced ongoing pain. Biomed Pharmacother. 2020;129:110374.PubMedCrossRef
70.
go back to reference Ye L, Hong F, Ze X, et al. Toxic effects of TiO2 nanoparticles in primary cultured rat sertoli cells are mediated via a dysregulated Ca2+ /PKC/p38 MAPK/NF-κB cascade. J Biomed Mater Res. 2017;105(5):1374–82.CrossRef Ye L, Hong F, Ze X, et al. Toxic effects of TiO2 nanoparticles in primary cultured rat sertoli cells are mediated via a dysregulated Ca2+ /PKC/p38 MAPK/NF-κB cascade. J Biomed Mater Res. 2017;105(5):1374–82.CrossRef
71.
go back to reference Park J, Kim SH, Cho D, Kim TS. Formononetin, a phytooestrogen, and its metabolites up-regulate interleukin-4 production in activated T cells via increased AP-1 DNA binding activity. Immunology. 2005;116(1):71–81.PubMedPubMedCentralCrossRef Park J, Kim SH, Cho D, Kim TS. Formononetin, a phytooestrogen, and its metabolites up-regulate interleukin-4 production in activated T cells via increased AP-1 DNA binding activity. Immunology. 2005;116(1):71–81.PubMedPubMedCentralCrossRef
72.
go back to reference Mizushima T, Obata K, Yamanaka H, et al. Activation of p38 MAPK in primary afferent neurons by noxious stimulation and its involvement in the development of thermal hyperalgesia. Pain. 2005;113(1–2):51–60.PubMedCrossRef Mizushima T, Obata K, Yamanaka H, et al. Activation of p38 MAPK in primary afferent neurons by noxious stimulation and its involvement in the development of thermal hyperalgesia. Pain. 2005;113(1–2):51–60.PubMedCrossRef
Metadata
Title
Corydalis saxicola Bunting total alkaloids attenuate paclitaxel-induced peripheral neuropathy through PKCε/p38 MAPK/TRPV1 signaling pathway
Authors
Chu Xue
Si-Xue Liu
Jie Hu
Jin Huang
Hong-Min Liu
Zhi-Xia Qiu
Fang Huang
Publication date
01-12-2021
Publisher
BioMed Central
Published in
Chinese Medicine / Issue 1/2021
Electronic ISSN: 1749-8546
DOI
https://doi.org/10.1186/s13020-021-00468-5

Other articles of this Issue 1/2021

Chinese Medicine 1/2021 Go to the issue