СУЧАСНІ ПОГЛЯДИ НА ВЗАЄМОЗВ'ЯЗКИ МОРФОФУНКЦІОНАЛЬНОГО СТАНУ ПЕЧІНКИ, СЕЛЕЗІНКИ ТА ГОЛОВНОГО МОЗКУ ЗА УМОВ ІШЕМІЇ-РЕПЕРФУЗІЇ ОСТАННЬОГО
DOI:
https://doi.org/10.24061/1727-4338.XVIII.4.70.2019.20Ключові слова:
церебральна ішемія-реперфузія, печінка, селезінкаАнотація
Мета роботи - проаналізувати дані літератури стосовно взаємозв'язків міжішемічно-реперфузійними пошкодженнями головного мозку та морфофункціональним станом печінки і селезінки.
Висновок. Аналіз наявних у літературі наукових фактів переконливо доводить
наявність двобічних взаємозв'язків між ішемічно-реперфузійним ушкодженням
головного мозку та морфофункціональним станом печінки і селезінки.
Посилання
1.Niu WM, Liu ZB, Yang XH, Wang Y, Shi HL. Effect on
CATmRNA expression in cerebral ischemia reperfusion rat with
hepatic injury treated by protecting liver to nourish brain therapy.
Liaoning J Tradit Chin Med. 2013;40:342-4.
2.Zhao W, Li FJ, Wang S. Protective effects of chrysophanol
on liver injury induced by cerebral ischemia-reperfusion in mice.
Acta Neuropharmacol. 2014;4:1-9.
3.Zhong WH, Qian KJ, Xiong JB, Ma K, Wang AZ, Zou Y.
Curcumin alleviates lipopolysaccharide induced sepsis and liver
failure by suppression of oxidative stress-related inflammation via
PI3K/AKT and NF-?B related signaling. Biomed Pharmacother.
2016;83:302-13. doi: 10.1016/j.biopha.2016.06.036
4.Lin MS, Miao HL, Gong XG, Bao ST. Effect of L-arginine
on calcium in hepatic mitochondrion in rats with obstructive
jaundice. Hepatobiliary Pancreat Dis Int. 2006;5(3):432-5.
5.Yang XF, He W, Lu WH, Zeng FD. Effects of scutellarin on
liver function after brain ischemia/reperfusion in rats. Acta
Pharmacol Sin. 2003;24(11):1118-24.
6.Chen J, Li Z, Hatcher JT, Chen QH, Chen L, Wurster RD, et
al. Deletion of TRPC6 Attenuates NMDA Receptor-Mediated Ca2+
Entry and Ca2+-Induced Neurotoxicity Following Cerebral Ischemia and Oxygen-Glucose Deprivation. Front Neurosci [Internet].
2017[cited 2019 Jan 19];11:138. Available from: https://www.
ncbi.nlm.nih.gov/pmc/articles/PMC5368256/pdf/fnins-11-00138.
pdf doi: 10.3389/fnins.2017.00138
7.You J, Feng L, Xin M, Ma D, Feng J. Cerebral Ischemic
Postconditioning Plays a Neuroprotective Role through Regulation
of Central and Peripheral Glutamate. Biomed Res Int [Internet].
2018[cited 2019 Feb 11];2018:6316059. Available from: https://
www.hindawi.com/journals/bmri/2018/6316059/ doi: 10.1155/
2018/6316059
8.Campos F, Rodríguez-Yáñez M, Castellanos M, Arias S,
Pérez-Mato M, Sobrino T, et al. Blood levels of glutamate oxaloacetate transaminase are more strongly associated with good
outcome in acute ischaemic stroke than glutamate pyruvate transaminase levels. Clin Sci (Lond). 2011;121(1):11-7. doi: 10.1042/
CS20100427
9.Campos F, Sobrino T, Ramos-Cabrer P, Castellanos M,
Blanco M, Rodríguez-Yáñez M, et al. High blood glutamate oxaloacetate transaminase levels are associated with good functional
outcome in acute ischemic stroke. J Cereb Blood Flow Metab.
2011;31(6):1387-93. doi: 10.1038/jcbfm.2011.4
10.Riehle KJ, Dan YY, Campbell JS, Fausto N. New concepts in
liver regeneration. J Gastroenterol Hepatol. 2011;26(Suppl 1):203-
12. doi: 10.1111/j.1440-1746.2010.06539.x
11.Zhou W, Chen X, Zhao G, Xu D, Jiang Z, Zhang L, et al.
Psoralen Induced Liver Injury by Attenuating Liver Regenerative
Capability. Front Pharmacol [Internet]. 2018[cited 2019 Feb 11];9:
1179. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/
PMC6232894/pdf/fphar-09-01179.pdf doi: 10.3389/fphar. 2018.
01179
12.Böhm F, Köhler UA, Speicher T, Werner S. Regulation of
liver regeneration by growth factors and cytokines. EMBO. Mol
Med. 2010;2(8):294-305. doi: 10.1002/emmm.201000085
13. Liu SQ, Tefft BJ, Roberts DT, Zhang LQ, Ren Y, Li YC,
et al. Cardioprotective proteins upregulated in the liver in response
to experimental myocardial ischemia. Am J Physiol Heart Circ
Physiol [Internet]. 2012[cited 2019 Jan 17];303(12):H1446-58.
Available from: https://www.physiology.org/doi/pdf/10.1152/
ajpheart.00362.2012 doi: 10.1152/ajpheart.00362.2012
14. Liu SQ, Roberts D, Zhang B, Ren Y, Zhang LQ, Wu YH.
Trefoil factor 3 as an endocrine neuroprotective factor from the
liver in experimental cerebral ischemia/reperfusion injury. PLoS
One [Internet]. 2013[cited 2019 Jan 17];8(10):e77732. Available
from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799633/
pdf/pone.0077732.pdf doi: 10.1371/journal.pone.0077732
15. Aboutaleb N, Shamsaei N, Rajabi H, Khaksari M, Erfani S,
Nikbakht F, et al. Protection of Hippocampal CA1 Neurons
Against Ischemia/Reperfusion Injury by Exercise Preconditioning
via Modulation of Bax/Bcl-2 Ratio and Prevention of Caspase-3
Activation. Basic Clin Neurosci. 2016;7(1):21-9.
16.Dziodzio T, Biebl M, Pratschke J. Impact of brain death on
ischemia/reperfusion injury in liver transplantation. Curr Opin
Organ Transplant. 2014;19(2):108-14. doi: 10.1097/MOT.0000
000000000061
17.Pirnik Z, Bundzikova J, Francisty T, Cibulova E, Lackovicova L, Mravec B, et al. Effect of liver ischemia-reperfusion
injury on the activity of neurons in the rat brain. Cell Mol
Neurobiol. 2009;29(6-7):951-60. doi: 10.1007/s10571-009-9381-
7
18.Bundzikova J, Pirnik Z, Lackovicova L, Mravec B, Kiss A.
Activation of Different Neuronal Phenotypes in the Rat Brain
Induced by Liver Ischemia-Reperfusion Injury: Dual Fos/Neuropeptide Immunohistochemistry. Cell Mol Neurobiol. 2011;31 (2):
293-301. doi: 10.1007/s10571-010-9621-x
19.Ostrowski RP, Schulte RW, Nie Y, Ling T, Lee T, Manaenko
A, et al. Acute splenic irradiation reduces brain injury in the rat
focal ischemic stroke model. Transl Stroke Res. 2012;3(4):473-81.
doi: 10.1007/s12975-012-0206-5
20.Offner H, Vandenbark AA, Hurn PD. Effect of experimental stroke on peripheral immunity: CNS ischemia induces
profound immunosuppression. Neuroscience. 2009;158(3):1098-
111. doi: 10.1016/j.neuroscience.2008.05.033
21.Marcet P, Santos N, Borlongan CV. When friend turns foe:
central and peripheral neuroinflammation in central nervous
system injury. Neuroimmunol Neuroinflamm. 2017; 4:82-92. doi:
10.20517/2347-8659.2017.07
22.Ajmo CT Jr, Collier LA, Leonardo CC, Hall AA, Green SM,
Womble TA, et al. Blockade of adrenoreceptors inhibits the splenic
response to stroke. Exp Neurol. 2009;218(1):47-55. doi: 10.1016/
j.expneurol.2009.03.044
23.Rasouli J, Lekhraj R, Ozbalik M, Lalezari P, Casper D. Brainspleen inflammatory coupling: a literature review. Einstein J Biol
Med. 2011;27(2):74-7. doi: 10.23861/EJBM20112768
24.Offner H, Subramanian S, Parker SM, Afentoulis ME,
Vandenbark AA, Hurn PD. Experimental stroke induces massive,
rapid activation of the peripheral immune system. J Cereb Blood
Flow Metab. 2006;26(5):654-65. doi: 10.1038/sj.jcbfm.9600217
25.Seifert HA, Leonardo CC, Hall AA, Rowe DD, Collier LA,
Benkovic SA, et al. The spleen contributes to stroke induced
neurodegeneration through interferon gamma signaling. Metab
Brain Dis. 2012;27(2):131-41. doi: 10.1007/s11011-012-9283-0
26.Chernykh YeR, Shevela YeYa, Morozov SA, Ostanin AA.
Immunopatogeneticheskiye aspekty ishemicheskogo insul'ta [Immunopathogenetic aspects of ischemic stroke]. Meditsinskaya
immunologiya, 2018;20(1):19-34.(in Russian)
27.Planas AM, Gomez-Choco M, Urra X, Gorina R, Caballero
M, Chamorro А. Brain-derived antigens in lymphoid tissue of patients with acute stroke. J Immunol. 2012;188(5):2156-63. doi:
10.4049/jimmunol.1102289
28.Dotson AL, Wang J, Saugstad J, Murphy SJ, Offner H.
Splenectomy reduces infarct volume and neuroinflammation in
male but not female mice in experimental stroke. J Neuroimmunol.
2015;278:289-98. doi: 10.1016/j.jneuroim.2014.11.020
29.Zhang BJ, Men XJ, Lu ZQ, Li HY, Qiu W, Hu XQ.
Splenectomy protects experimental rats from cerebral damage
after stroke due to anti-inflammatory effects. Chin Med J (Engl).
2013;126(12):2354-60.
30.Vahidy FS, Parsha KN, Rahbar MH, Lee M, Bui TT, Nguyen
C, et al. Acute splenic responses in patients with ischemic stroke
and intracerebral hemorrhage. J Cereb Blood Flow Metab. 2016;
36(6):1012-21. doi: 10.1177/0271678X15607880
31.Ran Y, Liu Z, Huang S, Shen J, Li F, Zhang W, et al. Splenectomy Fails to Provide Long-Term Protection Against Ischemic
Stroke. Aging Dis. 2018;9(3):467-9. doi: 10.14336/AD.2018.0130
32.Seifert HA, Hall AA, Chapman CB, Collier LA, Willing AE,
Pennypacker KR. A transient decrease in spleen size following
stroke corresponds to splenocyte release into systemic circulation.
J Neuroimmune Pharmacol. 2012;7(4):1017-24. doi: 10.1007/
s11481-012-9406-8
33.Offner H, Subramanian S, Parker SM, Wang C, Afentoulis
ME, Lewis A, et al. Splenic atrophy in experimental stroke is accompanied by increased regulatory T cells and circulating macrophages. J Immunol. 2006;176(11):6523-31.
34.Bao Y, Kim E, Bhosle S, Mehta H, Cho S. A role for spleen
monocytes in post-ischemic brain inflammation and injury. J
Neuroinflammation [Internet]. 2010[cited 2019 Jan 20];7:92.
Available from: https://jneuroinflammation.biomedcentral.com/
track/pdf/10.1186/1742-2094-7-92 doi: 10.1186/1742-2094-7-92
35.Grisanti LA, Perez DM, Porter JE. Modulation of immune
cell function by alpha(1)-adrenergic receptor activation. Curr Top
Membr. 2011;67:113-38. doi: 10.1016/B978-0-12-384921-2.000
06-9
36.Chiu NL, Kaiser B, Nguyen YV, Welbourne S, Lall C,
Cramer CC. The volume of the spleen and its correlates after acute
stroke. J Stroke Cerebrovasc Dis. 2016;25(12):2958-61. doi: 10.10
16/j.jstrokecerebrovasdis.2016.08.012
37.Famakin BM. The immune response to acute focal cerebral
ischemia and associated post-stroke immunodepression: a focused
review. Aging Dis. 2014;5(5):307-26. doi: 10.14336/AD.2014.050
0307
38.Chauhan A, Al Mamun A, Spiegel G, Harris N, Zhu L,
McCullough LD. Splenectomy protects aged mice from injury after
experimental stroke. Neurobiol Aging. 2018;61:102-11. doi: 10.10
16/j.neurobiolaging.2017.09.022
39.Fathali N, Ostrowski RP, Hasegawa Y, Lekic T, Tang J,
Zhang JH. Splenic immune cells in experimental neonatal hypoxiaischemia. Transl Stroke Res. 2013;4(2):208-19. doi: 10.1007/
s12975-012-0239-9
40.Pennypacker KR, Offner H. The role of the spleen in ischemic stroke. J Cereb Blood Flow Metab. 2015;35(2):186-7. doi:
10.1038/jcbfm.2014.212
##submission.downloads##
Опубліковано
Номер
Розділ
Ліцензія
Авторське право (c) 2020 O. V. Тkachuk, S. S. Тkachuk, S. S. Тkachuk, S. S. Тkachuk, S. S. Тkachuk, S. S. Тkachuk, S. S. Тkachuk, M. A. Povar, M. A. Povar, M. A. Povar, M. A. Povar, M. A. Povar, M. A. Povar, V. I. Shtefaniuk, V. I. Shtefaniuk, V. I. Shtefaniuk, V. I. Shtefaniuk, V. I. Shtefaniuk, V. I. Shtefaniuk
Ця робота ліцензується відповідно до Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Часопис користується «Типовим шаблоном положення про авторські права».
