Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*
Back to article page
Acupuncture Research|Updated:2021-09-01
|
Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*
Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*
Chinese Journal of Integrative Medicine2021年27卷第6期 页码:446-454
Affiliations:
1.Key Laboratory of Acupuncture Instrument, Fujian Academy of Chinese Medical Sciences, Fuzhou (350003), China
2.Fujian Key Laboratory of Propagated Sensation along Meridian, Institute of Meridians and Collaterals Medicine, Fujian Academy of Chinese Medical Sciences, Fuzhou (350003), China
Author bio:
Associate Prof. CHEN Xuan, E-mail:chenxuanfz@aliyun.com
Funds:
the National Natural Science Foundation of China(81503657;81373733);the Basic Research Project of Public Welfare Research Institutes in Fujian Province(2016R1033-6)
Xiao-qing HUANG, Jin-sen XU, Xiao-ran YE, 等. Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*[J]. Chinese Journal of Integrative Medicine, 2021,27(6):446-454.
Xiao-qing HUANG, Jin-sen XU, Xiao-ran YE, et al. Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*[J]. Chinese Journal of Integrative Medicine, 2021,27(6):446-454.
Xiao-qing HUANG, Jin-sen XU, Xiao-ran YE, 等. Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*[J]. Chinese Journal of Integrative Medicine, 2021,27(6):446-454. DOI: 10.1007/s11655-021-2865-0.
Xiao-qing HUANG, Jin-sen XU, Xiao-ran YE, et al. Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*[J]. Chinese Journal of Integrative Medicine, 2021,27(6):446-454. DOI: 10.1007/s11655-021-2865-0.
Wide Pulse Width Electroacupuncture Ameliorates Denervation-Induced Skeletal Muscle Atrophy in Rats via IGF-1/PI3K/Akt Pathway*
摘要
Abstract
Objective:
2
To evaluate the effect of the pulse width of electroacupuncture (EA) in the treatment of denervation-induced skeletal muscle atrophy in rats and examine the role of insulin-like growth factor 1 (IGF-1)/phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathway during EA.
Methods:
2
Sciatic nerve functional index (SFI)
muscle wet weight and the cross-sectional area (CSA) of the gastrocnemius muscle were analyzed after treatment in model rats with EA of various pulse widths (0.5
50
100 and 200 ms). The apoptosis index (AI) and paired box (PAX) 3 and PAX7 protein expression were also determined. Further
the mRNA and protein expressions of components of IGF-1/PI3K/Akt pathway and their downstream targets were determined
along with the inhibiting effect of the pathway with a PI3-specific inhibitor.
Results:
2
EA with a pulse width of 200 ms was found to have the best effect with regard to increasing SFI
CSA and muscle weight
decreasing AI
and increasing the expression of PAX3 and PAX7. The IGF-1/PI3K/Akt pathway was found to be activated by denervation
although the downstream forkhead box O (FoxO) pathway was not suppressed by its activation. The PI3K/Akt pathway and its downstream molecule mammalian target of rapamycin (mTOR) were up-regulated further by EA to promote muscle protein synthesis. Meanwhile
the expressions of downstream FoxO and F-box protein 32 (ATROGIN-1) were down-regulated to reduce protein degradation.
Conclusions:
2
EA with 200-ms pulse width was found to have a more significant effect than 0.5-ms EA. The positive effects of EA disappeared after inhibition of the PI3K/Akt pathway.
JS Petrofsky. The training effects of wide pulse width electrical stimulation on denervated muscle. J Neurol Rehabil 1991;5:161-167.
H Kern, C Hofer, M Modlin, C Forstner, D Raschka-Hogler, W Mayr, et al. Denervated muscles in humans: limitations and problems of currently used functional electrical stimulation training protocols. Artif Organs 2002;26:216-218.
TE Salazar, MR Richardson, E Beli, MS Ripsch, J George, Y Kim, et al. Electroacupuncture promotes central nervous system-dependent release of mesenchymal stem cells.Stem Cells 2017;35:1303-1315.
M Modlin, C Forstner, C Hofer, W Mayr, W Richter, U Carraro, et al. Electrical stimulation of denervated muscles: first results of a clinical study. Artif Organs 2005;29:203-206.
H Kern, C Hofer, S Loefler. Atrophy, ultra-structural disorders, severe atrophy and degeneration of denervated human muscle in SCI and aging. Implications for their recovery by functional electrical stimulation, updated 2017.Neurol Res 2017;39:660-666.
ES Koh, HC Kim, JY Lim. The effects of electromyostimulation application timing on denervated skeletal muscle atrophy. Muscle Nerve 2017;56:e154-161.
BS Guo, KK Cheung, SS Yeung, BT Zhang, EW Yeung.Electrical stimulation influences satellite cell proliferation and apoptosis in unloading-induced muscle atrophy in mice.PloS One 2012;7:e30348.
AS Gorgey, RE Khalil, RM Lester, GA Dudley, DR Gater.Paradigms of lower extremity electrical stimulation training after spinal cord injury. J Vis Exp 2018;132:57000.
HL Su, CY Chiang, ZH Lu, FC Cheng, CJ Chen, ML Sheu, et al. Late administration of high-frequency electrical stimulation increases nerve regeneration without aggravating neuropathic pain in a nerve crush injury. Neurol Res 2018;19:37.
YT Zhang, H Jin, JH Wang, LY Wen, Y Yang, JW Ruan, et al.Tail nerve electrical stimulation and electro-acupuncture can protect spinal motor neurons and alleviate muscle atrophy after spinal cord transection in rats. Neural Plast 2017;2017:7351238.
Z Su, L Hu, J Cheng, JD Klein, F Hassounah, H Cai, et al.Acupuncture plus low-frequency electrical stimulation (Acu-LFES) attenuates denervation-induced muscle atrophy. J Appl Physiol 2016;20:426-436.
M Zhang, Y Zhang, Y Bian, H Fu, Y Xu, Y Guo. Effect of long-term electroacupuncture stimulation on recovery of sensorimotor function after peripheral nerve anastomosis. Acupunct Med 2018;36:170-175.
J Yu, M Wang, J Liu, X Zhang, S Yang. Effect of electroacupuncture on the expression of agrin and acetylcholine receptor subtypes in rats with tibialis anterior muscular atrophy induced by sciatic nerve injection injury.Acupunct Med 2017;35:268-275.
H Kern, S Boncompagni, K Rossini, W Mayr, G Fano, ME Zanin, et al. Long-term denervation in humans causes degeneration of both contractile and excitation-contraction coupling apparatus, which is reversible by functional electrical stimulation (FES): a role for myofiber regeneration? J Neuropathol Exp Neurol 2004;63:919-931.
DJ Glass. PI3 kinase regulation of skeletal muscle hypertrophy and atrophy. Curr Top Microbiol Immunol 2010;346:267-278.
SC Bodine, TN Stitt, M Gonzalez, WO Kline, GL Stover, R Bauerlein, et al. Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo. Nat Cell Biol 2001;3:1014-1019.
LT Timmer, WMH Hoogaars, RT Jaspers. The role of IGF-1 signaling in skeletal muscle atrophy. Adv Exp Med Biol 2018;1088:109-137.
JR Bain, SE Mackinnon, DA Hunter. Functional evaluation of complete sciatic, peroneal, and posterior tibial nerve lesions in the rat. Plast Reconstr Surg 1989;83:129-138.
CRS Banerji, M Panamarova, H Hebaishi, RB White. PAX7 target genes are globally repressed in facioscapulohumeral muscular dystrophy skeletal muscle. Nat Commun 2017;8:2152.
Z Su, A Robinson, L Hu, JD Klein, F Hassounah, M Li, et al.Acupuncture plus low-frequency electrical stimulation (Acu-LFES) attenuates diabetic myopathy by enhancing muscle regeneration. PloS One 2015;10:e0134511.
M Olive, JA Martinez-Matos, P Pirretas, M Povedano, C Navarro, I Ferrer. Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders.Neuropathol Appl Neurobiol 1997;23:475-482.
M Sharma, R Kambadur, Z Li, L Naslund-Koch, C Henriquez-Olguin, JR Knudsen, et al. Chemical denervation using botulinum toxin increases Akt expression and reduces submaximal insulin-stimulated glucose transport in mouse muscle. Nat Commun 2018;53:224-233.
EM MacDonald, E Andres-Mateos, R Mejias, JL Simmers, R Mi, JS Park, et al. Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition. Dis Model Mech 2014;7:471-481.
RY Cao, J Li, Q Dai, Q Li, J Yang. Muscle atrophy: present and future. Nat Commun 2018;1088:605-624.
Electroacupuncture Promotes Functional Recovery after Facial Nerve Injury in Rats by Regulating Autophagy via GDNF and PI3K/mTOR Signaling Pathway
Electroacupuncture at Sensitized Acupoints Relieves Somatic Referred Pain in Colitis Rats by Inhibiting Sympathetic-Sensory Coupling to Interfere with 5-HT Signaling Pathway
Electroacupuncture Improves Blood-Brain Barrier and Hippocampal Neuroinflammation in SAMP8 Mice by Inhibiting HMGB1/TLR4 and RAGE/NADPH Signaling Pathways
Electroacupuncture Alleviates Functional Constipation in Mice by Activating Enteric Glial Cell Autophagy via PI3K/AKT/mTOR Signaling
Molecular Mechanism of Electroacupuncture Regulating Cerebral Arterial Contractile Protein in Rats with Cerebral Infarction Based on MLCK Pathway
相关作者
暂无数据
相关机构
Academic Affairs Office, Chengdu University of Traditional Chinese Medicine
Department of Rehabilitation Medicine, Guanghan People's Hospital
Acupuncture and Tuina School, Chengdu University of Traditional Chinese Medicine
Department of Neurology, the First Affiliated Hospital of Chengdu Medical College
Department of Rehabilitation Medicine, West China Hospital, Sichuan University/West China School of Nursing, Sichuan University