Protective effect of rutin on myelin sheath injury in the sciatic nerve of rats induced by acrylamide

BAI Yanxian JIA Hui ZHANG Tong LUO Yu-you ZHANG Chun-mei LUO Li MA Yu-xin LIU Jing

Acta Anatomica Sinica ›› 2022, Vol. 53 ›› Issue (2) : 166-172.

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Acta Anatomica Sinica ›› 2022, Vol. 53 ›› Issue (2) : 166-172. DOI: 10.16098/j.issn.0529-1356.2022.02.005

Protective effect of rutin on myelin sheath injury in the sciatic nerve of rats induced by acrylamide

  • BAI Yanxian  JIA Hui  ZHANG Tong  LUO Yu-you  ZHANG Chun-mei  LUO Li MA Yu-xin LIU Jing*#br# #br#
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Abstract

Objective To investigate the effect of rutin (Rut) on sciatic nerve myelin injury induced by acrylamide(ACR), and to observe the changes of myelin structure, myelin basic protein (MBP) and myelin associated glycoprotein (MAG) in rats exposed to ACR.
Methods Thirty-six adult male SD rats were randomly divided into 4 groups: control group (ddH2O), 20 mg/kg ACR exposure group (ACR), 100 mg/kg Rut pre-protection ACR exposure group (R1+ACR), 200 mg/kg Rut pre-protection ACR exposure group (R2+ACR), 9 rats in each group, and were given gastric gavage for 21 days. HE staining and transmission electron microscopy were used to observe the changes of the sciatic nerve myelin sheath structure, immunohistochemistry and Western blotting were used to detect the changes in the expression of MBP and MAG in each group of rats.   Results Hind limb distance measurement showed that compared with the control group, the hind limb distance of rats in the ACR group increased with the prolonged exposure time (P<0.05). After pre-protection with Rut, the hind limb distance of the R1+ACR and R2+ACR groups was significantly lower than that in the ACR group. HE staining showed that after ACR was infected, nerve fibers were disordered and myelin swelling appeared, while in R2+ACR group, nerve fibers were orderly and myelin swelling was reduced. Transmission electron microscopy showed that the myelin in ACR group was swollen and loosened, vacuoles were found in the interlamellar area, and some axons had vacuolar degeneration. Compared with the ACR group, the laxity of myelin in the R2+ACR group was improved and vacuolar degeneration was not obvious, and only a few vacuoles were found in the myelin lamina and axons. Immunohistochemistry and Western blotting results showed that the expression levels of MBP and MAG in the ACR group decreased significantly compared with the control group (P<0.01), compared with ACR group, the expression levels of MBP and MAG in R1+ACR group and R2+ACR group increased (P<0.05).   Conclusion Rut has a protective effect on myelin sheath in the sciatic nerve of rats induced by acrylamide, which may be related to the inhibition of Rut on the decreased expression of MBP and MAG in the sciatic nerve induced by ACR.

Key words

Acrylamide / Rutin / Sciatic nerve / Myelin basic protein / Myelin associated glycoprotein / Immunohistochemistry / Western blotting / Rat

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BAI Yanxian JIA Hui ZHANG Tong LUO Yu-you ZHANG Chun-mei LUO Li MA Yu-xin LIU Jing. Protective effect of rutin on myelin sheath injury in the sciatic nerve of rats induced by acrylamide[J]. Acta Anatomica Sinica. 2022, 53(2): 166-172 https://doi.org/10.16098/j.issn.0529-1356.2022.02.005

References

[1] Friedman M. Chemistry, biochemistry, and safety of acrylamide. A review [J]. J Agric Food Chem, 2003, 51(16):4504-4526.
[2] Erkekoglu P, Baydar T. Acrylamide neurotoxicity [J]. Nutr Neurosci, 2014, 17(2):49-57. 
[3] Kjuus H, Goffeng LO, Heier MS, et al. Effects on the peripheral nervous system of tunnel workers exposed to acrylamide and N-methylolacrylamide [J]. Scand J Work Environ Health, 2004, 30(1):21-29. 
[4] Poutoglidou F, Piagkou M, Totlis T, et al. Sciatic nerve variants and the piriformis muscle: a systematic review and meta-analysis [J]. Cureus, 2020, 12(11):e11531.
[5] Gu ZT, Jia H, Liu J, et al. Effects of acrylamide on the expression of MBP and MAG in sciatic nerve of rats [J]. Chinese Journal of Neuroanatomy, 2019, 35(1):29-34. (in Chinese)
古梓婷,贾会,刘靖,等,丙烯酰胺染毒对大鼠坐骨神经MBP和MAG表达的影响 [J]. 神经解剖学杂志,2019,35(1):29-34.
[6] Tabeshpour J, Mehri S, Abnous K, et al. Role of oxidative stress, MAPKinase and apoptosis pathways in the protective effects of thymoquinone against acrylamideinduced central nervous system toxicity in rat [J]. Neurochem Res, 2020, 45(2):254-267.
[7] Budzynska B, Faggio C, Kruk-Slomka M, et al. Rutin as neuroprotective agent: from bench to bedside [J]. Curr Med Chem, 2019, 26(27):5152-5164. 
[8] Ya?ar H, Ersoy A, Cimen FK, et al. Peripheral neurotoxic effects of cisplatin on rats and treatment with rutin [J]. Adv Clin Exp Med, 2019, 28(11):1537-1543. 
[9] Motamedshariaty VS, Amel Farzad S, Nassiri-Asl M, et al. Effects of rutin on acrylamide-induced neurotoxicity [J]. Daru,2014, 22(1):27.
[10] Bishnoi M, Chopra K, Kulkarni SK. Protective effect of rutin, a polyphenolic flavonoid against haloperidol-induced orofacial dyskinesia and associated behavioural, biochemical and neurochemical changes [J]. Fundam Clin Pharmacol, 2007, 21(5):521-529. 
[11] Koszucka A, Nowak A. Thermal processing food-related toxicants: a review [J]. Crit Rev Food Sci Nutr, 2019, 59(22):3579-3596. 
[12] Bin-Jumah M, Abdel-Fattah AM, Saied EM, et al. Acrylamide-induced peripheral neuropathy: manifestations, mechanisms, and potential treatment modalities [J]. Environ Sci Pollut Res Int, 2021, 28(11):13031-13046.
[13] Ahmad Bainmahfouz FR, Ali SS, Al-Shali RA, et al. Vitamin E and 5-amino salicylic acid ameliorates acrylamide-induced peripheral neuropathy by inhibiting caspase-3 and inducible nitric oxide synthase immunoexpression [J]. J Chem Neuroanat,2021, 113:101935. 
[14] Lopachin RM, Gavin T. Acrylamide-induced nerve terminal damage: relevance to neurotoxic and neurodegenerative mechanisms [J]. J Agric Food Chem, 2008, 56(15):5994-6003.
[15] Kjuus H, Goffeng LO, Heier MS, et al. Effects on the peripheral nervous system of tunnel workers exposed to acrylamide and N-methylolacrylamide [J]. Scand J Work Environ Health, 2004, 30(1):21-29.
[16] Ronzano R, Thetiot M, Lubetzki C, et al. Myelin plasticity and repair: neuro-glial choir sets the tuning. front cell neurosci [J]. Front Cell Neurosci,2020, 14:42.
[17] Gould RM, Oakley T, Goldstone JV, et al. Myelin sheaths are formed with proteins that originated in vertebrate lineages [J]. Neuron Glia Biol, 2008, 4(2):137-152.
[18] Shen D, Zhang Q, Gao X, et al. Age-related changes in myelin morphology, electrophysiological property and myelin-associated protein expression of mouse sciatic nerves [J]. Neurosci Lett, 2011, 502(3):162-167.
[19] Zhang Q, Song W, Zhao B, et al. Quercetin attenuates diabetic peripheral neuropathy by correcting mitochondrial abnormality via activation of AMPK/PGC-1α pathway in vivo and in vitro [J]. Front Neurosci, 2021, 15:636172.
[20] Pronker MF, Lemstra S, Snijder J, et al. Structural basis of myelin-associated glycoprotein adhesion and signalling [J]. Nat Commun, 2016, 7:13584.
[21] Tomita K, Kubo T, Matsuda K, et al. Myelin-associated glycoprotein reduces axonal branching and enhances functional recovery after sciatic nerve transection in rats [J]. Glia, 2007, 55(14):1498-1507.
[22] Zhu X, Li K, Guo X, et al. Schwann cell proliferation and differentiation that is induced by ferulic acid through MEK1/ERK1/2 signalling promotes peripheral nerve remyelination following crush injury in rats [J]. Exp Ther Med, 2016, 12(3):1915-1921.
[23] Tabeshpour J, Mehri S, Abnous K, et al. Neuroprotective effects of thymoquinone in acrylamide-induced peripheral nervous system toxicity through MAPKinase and apoptosis pathways in rat [J]. Neurochem Res, 2019, 44(5):1101-1112.
[24] Hichor M, Sampathkumar NK, Montanaro J, et al. Paraquat induces peripheral myelin disruption and locomotor defects: crosstalk with LXR and Wnt pathways [J]. Antioxid Redox Signal, 2017, 27(3):168-183.
[25] Ahmed MM, Hussein MMA. Neurotoxic effects of silver nanoparticles and the protective role of rutin [J]. Biomed Pharmacother, 2017, 90:731-739.
[26] Mittal R, Kumar A, Singh DP, et al. Ameliorative potential of rutin in combination with nimesulide in STZ model of diabetic neuropathy: targeting Nrf2/HO-1/NF-kB and COX signalling pathway [J]. Inflammopharmacology, 2018, 26(3):755-768.
[27] Thabet NM, Moustafa EM. Protective effect of rutin against brain injury induced by acrylamide or gamma radiation: role of PI3K/AKT/GSK-3β/NRF-2 signalling pathway [J]. Arch Physiol Biochem, 2018, 124(2):185-193.
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