Gender Peculiarities of Postresuscitation in the Expression of Brain-Derived Neurotrophic Factor (BDNF)
https://doi.org/10.15360/1813-9779-2017-5-44-57
Abstract
Purpose: to identify gender peculiarities of postresuscitation shifts in BDNF expression and neuronal death.
Materials and Methods. At different points of the postresuscitation period (days 1-, 4-, 7-, and 14), the condition of highly sensitive to hypoxia neuronal populations (pyramidal neurons of hippocampus and Purkinje cells of cerebellum) were studied in white mature female rats exposed to a 10-minute stop of systemic blood circulation (compression of vascular fascicle of the heart). Sham operated animals were used as the control. Immunohistochemical detection of BDNF-immunoreactive neurons followed with determination of optical density, number of cells with different levels of BDNF expression, and total count of neurons per 1 mm of the length of their layer was carried out. The work was done using the image analysis system (computer Intel, microscope Olympus BX-41, software ImadgeScopeM, ImageJ 1,48v, Excel 2007). Statistic processing of data was performed with the aid of Statistica 7.0 using Kolmogorov-Smirnov λ test, Mann-Whitney U test, and Student's t-test.
Results. The dynamics of postresuscitation shifts in BDNF-immunoreactivity of neuronal populations highly sensitive to hypoxia was studied in rats. Purkinje cells population in tissue slides from brain specimens harvested from female rats the alterations in BDNF expression became evident. This pattern was accompanied by the death of neurons. Those shifts in female animals were found to develop later than in male rats — by day 7 of the postresuscitation. Only BDNF-negative and BDNF-weakly positive neurons not survived postresuscitation. In the population of pyramidal cells of hippocampus in females, in contrast to males, there were no quantitative changes in BDNF molecules as revealed by immunohistochemistry and neuronal death process did not develop.
Conclusion. Gender peculiarities in the development of postresuscitation shifts in BDNF expression and associated therewith death of neurons were revealed. It was shown that after cardiac arrest of the same duration, the postresuscitation shifts in BDNF expression and neuronal death manifested mostly in males compared to females. At the same time, animals of both genders demonstrate common postresuscitation brain alterations evidencing connection between the level of BDNF expression in neurons and their resistance to ischemia-reperfusion. Gender-specific patterns of brain damage and their importance for understanding the mechanisms of post-hypoxic encephalopathies are discussed.
About the Authors
M. Sh. AvrushchenkoRussian Federation
25 Petrovka Str., Build. 2, Moscow 107031
I. V. Ostrova
Russian Federation
25 Petrovka Str., Build. 2, Moscow 107031
A. V. Grechko
Russian Federation
25 Petrovka Str., Build. 2, Moscow 107031
References
1. Volkov A.V., Avrushchenko M.Sh., Gorenkova N.A., Zarzhetsky Yu.V. Implication of sexual dimorphism and reproductive hormones in the pathogenesis and outcome of postresuscitative disease. Obshchaya Reanimatologiya = General Reanimatology. 2006; 2 (5-6): 70-78. DOI: 10.15360/1813-9779-2006-6-70-78. [In Russ., In Engl.]
2. Liu F., Li Z., Li J., Siegel C., Yuan R., McCullough L.D. Sex differences in caspase activation after stroke. Stroke. 2009; 40 (5): 1842–1848. DOI: 10.1161/STROKEAHA.108.538686. PMID: 19265047
3. Vagnerova K., Koerner I.P., Hurn P.D. Gender and the injured brain. Anesth. Analg. 2008; 107 (1): 201-214. DOI: 10.1213/ane.0b013e31817326a5. PMID: 18635489
4. Sakuma Y. Gonadal steroid action and brain sex differentiation in the rat. J. Neuroendocrinol. 2009; 21 (4): 410-414. DOI: 10.1111/j.1365-2826.2009.01856.x. PMID: 19226349
5. Zuo W., Zhang W., Chen N.H. Sexual dimorphism in cerebral ischemia injury. Eur. J. Pharmacol. 2013; 711 (1-3): 73-79. DOI: 10.1016/j.ejphar. 2013.04.024. PMID: 23652162
6. Herson P.S., Hurn P.D. Gender and the injured brain. Prog. Brain Res. 2010; 186: 177-187. DOI: 10.1016/B978-0-444-53630-3.00012-9. PMID: 21094893
7. Herson P.S., Palmateer J., Hurn P.D. Biological sex and mechanisms of ischemic brain injury. Transl. Stroke Res. 2013; 4 (4): 413-419. DOI: 10.1007/s12975-012-0238-x. PMID: 23930140
8. Tsukahara S., Kakeyama M., Toyofuku Y. Sex differences in the level of Bcl-2 family proteins and caspase-3 activation in the sexually dimorphic nuclei of the preoptic area in postnatal rats. J. Neurobiol. 2006; 66 (13): 1411-1419. DOI: 10.1002/neu.20276. PMID: 17013925
9. Gibson C.L. Cerebral ischemic stroke: is gender important? J. Cereb. Blood Flow Metab. 2013; 33 (9): 1355-1361. DOI: 10.1038/jcbfm. 2013.102. PMID: 23756694
10. Berretta A., Tzeng Y.C., Clarkson A.N. Post-stroke recovery: the role of activity-dependent release of brain-derived neurotrophic factor. Expert Rev. Neurother. 2014; 14 (11): 1335-1344. DOI: 10.1586/14737175. 2014.969242. PMID: 25319267
11. Blondeau N., Lipsky R.H., Bourourou M., Duncan M.W., Gorelick P.B., Marini A.M. Alpha-linolenic acid: an omega-3 fatty acid with neuroprotective properties-ready for use in the stroke clinic? Biomed. Res. Int. 2015; 2015: 519830. DOI:10.1155/2015/519830. PMID: 25789320
12. Budni J., Bellettini-Santos T., Mina F., Garcez M.L., Zugno A.I. The involvement of BDNF, NGF and GDNF in aging and Alzheimer’s disease. Aging Dis. 2015; 6 (5): 331-341. DOI: 10.14336/AD.2015.0825. PMID: 26425388
13. Khalin I., Alyautdin R., Kocherga G., Bakar M.A. Targeted delivery of brain-derived neurotrophic factor for the treatment of blindness and deafness. Int. J. Nanomedicine. 2015; 10: 3245-3267. DOI: 10.2147/IJN. S77480. PMID: 25995632
14. Dincheva I., Lynch N.B., Lee F.S. The role of BDNF in the development of fear learning. Depress Anxiety. 2016; 33 (10): 907-916. DOI: 10.1002/da.22497. PMID: 27699937
15. Larpthaveesarp A., Ferriero D.M., Gonzalez F.F. Growth factors for the treatment of ischemic brain injury (growth factor treatment). Brain Sci. 2015; 5 (2): 165-177. DOI: 10.3390/brainsci5020165. PMID: 25942688
16. Kimura A., Namekata K., Guo X., Harada C., Harada T. Neuroprotection, growth factors and BDNF-TrkB signalling in retinal degeneration. Int. J. Mol. Sci. 2016; 17 (9): pii: E1584. DOI: 10.3390/ijms17091584. PMID: 27657046
17. Hempstead B.L. Brain-derived neurotrophic factor: three ligands, many actions. Trans. Am. Clin. Climatol. Assoc. 2015; 126: 9-19. PMID: 26330656
18. Avrushchenko M.Sh., Ostrova I.V. Postresuscitative changes of BrainDerived Neurotrophic Factor (BDNF) protein expression: association with neuronal death. Obshchaya Reanimatologiya = General Reanimatology. 2017; 13 (4): 6-21. DOI: 10.15360/1813-9779-2017-4-6-21. [In Russ., In Engl.]
19. Korpachev V.G., Lysenkov S.P., Tel L.Z. Modeling clinical death and postresuscitation disease in rats. Patologicheskaya Fiziologiya i Eksperimentalnaya Terapiya. 1982; 3: 78-80. PMID: 7122145. [In Russ.]
20. Avrushchenko M.Sh., Ostrova I.V., Volkov A.V. Postresuscitation changes in the expression of Glial-Derived Neurotrophic Factor (GDNF): association with cerebellar Purkinje cell damage (an experimental study). Obshchaya Reanimatologiya = General Reanimatology. 2014; 10 (5): 59-68. DOI: 10.15360/1813-9779-2014-5-59-68. [In Russ., In Engl.]
21. Avruschenko M.Sh., Ostrova I.V. Association of glial cell line-derived neurotrophic factor (GDNF) protein expression with the neuronal death in post-resuscitation period. Resuscitation. 2014; 85: S108. DOI: 10.1016/j.resuscitation.2014.03.268
22. Ostrova I.V., Avrushchenko M.Sh., Volkov A.V. Association of GRP78 protein expression with the degree of postischemic hippocampal damage in rats of both sexes. Obshchaya Reanimatologiya = General Reanimatology. 2011; 7 (6): 28-33. DOI: 10.15360/1813-9779-2011-6-28. [In Russ., In Engl.]
23. Ostrova I.V., Avrushchenko M.Sh. Expression of Brain-Derived Neurotrophic Factor (BDNF) increases the resistance of neurons to death in the postresuscitation period. Obshchaya Reanimatologiya = General Reanimatology. 2015; 11 (3): 45-53. DOI: 10.15360/1813-9779-2015-3-45-53. [In Russ., In Engl.]
24. Chen G., Fan Z., Wang X., Ma C., Bower K.A., Shi X., Ke Z.J., Luo J. Brain-derived neurotrophic factor suppresses tunicamycin-induced upregulation of CHOP in neurons. J. Neurosci. Res. 2007; 85 (8): 1674-1684. DOI: 10.1002/jnr.21292. PMID: 17455323
25. Wei H.J., Xu J.H., Li M.H., Tang J.P., Zou W., Zhang P., Wang L., Wang C.Y., Tang X.Q. Hydrogen sulfide inhibits homocysteine-induced endoplasmic reticulum stress and neuronal apoptosis in rat hippocampus via upregulation of the BDNF-TrkB pathway. Acta Pharmacol. Sin. 2014; 35 (6): 707-715. DOI: 10.1038/aps.2013.197. PMID: 24747165
26. Kang J.S. Exercise copes with prolonged stress-induced impairment of spatial memory performance by endoplasmic reticulum stress. J. Exerc. Nutrition Biochem. 2015; 19 (3): 191-197. DOI: 10.5717/jenb.2015. 15080705. PMID: 26527209
27. Avrushchenko M.Sh., Ostrova I.V., Zarzhetsky Yu.V., Moroz V.V., Gudasheva T.A., Seredenin S.B. Effect of the nerve growth factor mimetic GK-2 on post-resuscitation expression of neurotrophic factors. Patologicheskaya Fiziologiya i Eksperimentalnaya Terapiya. 2015; 59 (2): 12-18. PMID: 26571801. [In Russ.]
28. Volkov A.V., Avrushchenko M.Sh., Barannik A.P., Ziganshin R.Kh., Gorenkova N.A., Zarzhetsky Yu.V. Sexual dimorphism of cerebral structural and functional changes in the early postresuscitative period after cardiac arrest. Obshchaya Reanimatologiya = General Reanimatology. 2006; 2 (2): 9-13. DOI: 10.15360/1813-9779-2006-2-9-13. [In Russ., In Engl.]
29. Volkov A.V., Avrushchenko M.Sh., Gorenkova N.A., Shcherbakova L.N., Zarzhetsky Yu.V. Sexual differences in delayed postresuscitative brain changes (experimental study). Obshchaya Reanimatologiya = General Reanimatology. 2007; 3 (5-6): 97-102. DOI: 10.15360/1813-9779-2007-6-97-102. [In Russ., In Engl.]
30. Ostrova I.V., Avrushchenko M.Sh., Volkov A.V., Zarzhetsky Yu.V. Gender differences in postresuscitative brain structural changes. Obshchaya Reanimatologiya = General Reanimatology. 2009; 5 (6): 60-65. DOI: 10.15360/1813-9779-2009-6-60. [In Russ., In Engl.]
31. Ostrova I.V., Avrushchenko M.Sh., Zarzhetsky Yu.V., Afanasyev A.V., Volkov A.V. Gender differences in postresuscitative brain injury and in the efficacy of the immunomodulator panavir. Obshchaya Reanimatologiya = General Reanimatology. 2010; 6 (6): 25-28. DOI: 10.15360/1813-9779-2010-6-25. [In Russ., In Engl.]
32. Alkayed N.J., Harukuni I., Kimes A.S., London E.D., Traystman R.J., Hurn P.D. Gender-linked brain injury in experimental stroke. Stroke. 1998; 29 (1): 159–166. DOI: 10.1161/01.STR.29.1.159. PMID: 9445346
33. Lieb K., Andrae J., Reisert I., Pilgrim C. Neurotoxicity of dopamine and protective effects of the NMDA receptor antagonist AP-5 differ between male and female dopaminergic neurons. Exp. Neurol. 1995; 134 (2): 222–229. DOI: 10.1006/exnr.1995.1052. PMID: 7556542
34. Du L., Bayir H., Lai Y., Zhang X., Kochanek P.M., Watkins S.C., Graham S.H., Clark R.S. Innate gender-based proclivity in response to cytotoxicity and programmed cell death pathway. J. Biol. Chem. 2004; 279 (37): 38563–38570. DOI: 10.1074/jbc.M405461200. PMID: 15234982
35. Arnold A.P., Rissman E.F., De Vries G.J. Two perspectives on the origin of sex differences in the brain. Ann. N Y Acad. Sci. 2003; 1007: 176–188. DOI: 10.1196/annals.1286.018. PMID: 14993052
36. McCullough L.D., Zeng Z., Blizzard K.K., Debchoudhury I., Hurn P.D. Ischemic nitric oxide and poly (ADPribose) polymerase-1 in cerebral ischemia: male toxicity, female protection. J. Cereb. Blood Flow Metab. 2005; 25 (4): 502–512. DOI: 10.1038/sj.jcbfm.9600059. PMID: 15689952
37. Kassell N.F., Haley E.C.Jr., Apperson-Hansen C., Alves W.M. Randomized, doubleblind, vehicle-controlled trial of tirilazad mesylate in patients with aneurysmal subarachnoid hemorrhage: a cooperative study in Europe, Australia, and New Zealand. J. Neurosurg. 1996; 84 (2): 221– 228. DOI: 10.3171/jns.1996.84.2.0221. PMID: 8592224
38. Suzuki T., Bramlett H.M., Dietrich W.D. The importance of gender on the beneficial effects of posttraumatic hypothermia. Exp. Neurol. 2003; 184 (2): 1017–1026. DOI: 10.1016/S0014-4886(03)00389-3. PMID: 14769396
39. Chavez-Valdez R., Martin L.J., Razdan S., Gauda E.B., Northington F.J. Sexual dimorphism in BDNF signaling after neonatal hypoxia-ischemia and treatment with necrostatin-1. Neuroscience. 2014; 260: 106-119. DOI: 10.1016/j.neuroscience.2013.12.023. PMID: 24361177
40. Ostrova I.V., Avrushchenko M.Sh., Volkov A.V. Gender differences in post-ischemic brain morphology are associated with expression level of HSP70 protein. Shock Society Fifth Congress of the European Shock Society (ESS) 2013, September 12-14, Vienna, Austria. SHOCK Supplement to the ESS Congress, Austria. 2013; 40 (Suppl 1): 29. DOI: 10.1097/SHK.0b013e3182a5906f
41. Cain S.W., Chang A.M., Vlasac I., Tare A., Anderson C., Czeisler C.A., Saxena R. Circadian rhythms in plasma brain-derived neurotrophic factor differ in men and women. J. Biol. Rhythms. 2017; 32 (1): 75-82. DOI: 10.1177/0748730417693124. PMID: 28326910
42. Brague J.C., Swann J.M. Sexual dimorphic expression of TrkB, TrkBT1, and BDNF in the medial preoptic area of the Syrian hamster. Brain Res. 2017; 1669: 122-125. DOI: 10.1016/j.brainres.2017.06.008. PMID: 28606780
43. Kight K.E., McCarthy M.M. Sex differences and estrogen regulation of BDNF gene expression, but not propeptide content, in the developing hippocampus. J. Neurosci. Res. 2017; 95 (1-2): 345-354. DOI: 10.1002/jnr.23920. PMID: 27870444
44. Atwi S., McMahon D., Scharfman H., MacLusky N.J. Androgen modulation of hippocampal structure and function. Neuroscientist. 2016; 22 (1): 46-60. DOI: 10.1177/1073858414558065. PMID: 25416742
45. Franklin T.B., Perrot-Sinal T.S. Sex and ovarian steroids modulate brainderived neurotrophic factor (BDNF) protein levels in rat hippocampus under stressful and non-stressful conditions. Psychoneuroendocrinology. 2006; 31 (1): 38-48. DOI: 10.1016/j. psyneuen.2005.05.008. PMID: 15996825
46. Carbone D.L., Handa R.J. Sex and stress hormone influences on the expression and activity of brain-derived neurotrophic factor. Neuroscience. 2013; 239: 295-303. DOI: 10.1016/j.neuroscience.2012. 10.073. PMID: 23211562
47. Miñano A., Xifró X., Pérez V., Barneda-Zahonero B., Saura C.A., Rodríguez-Alvarez J. Estradiol facilitates neurite maintenance by a Src/Ras/ERK signalling pathway. Mol. Cell Neurosci. 2008; 39 (2): 143–151. DOI: 10.1016/j.mcn.2008.06.001. PMID: 18620059
48. Bender R.A., Zhou L., Wilkars W., Fester L., Lanowski J.S., Paysen D., König A., Rune G.M. Roles of 17ss-estradiol involve regulation of reelin expression and synaptogenesis in the dentate gyrus. Cereb. Cortex. 2010; 20 (12): 2985–2995. DOI: 10.1093/cercor/bhq047. PMID: 20421250
49. Chan C.B., Ye K. Sex differences in brain-derived neurotrophic factor signaling and functions. J. Neurosci. Res. 2017; 95 (1-2): 328-335. DOI: 10.1002/jnr.23863. PMID: 27870419
50. Wei Y.C., Wang S.R., Xu X.H. Sex differences in brain-derived neurotrophic factor signaling: functions and implications. J. Neurosci. Res. 2017; 95 (1-2): 336-344. DOI: 10.1002/jnr.23897. PMID: 27870405
Review
For citations:
Avrushchenko M.Sh., Ostrova I.V., Grechko A.V. Gender Peculiarities of Postresuscitation in the Expression of Brain-Derived Neurotrophic Factor (BDNF). General Reanimatology. 2017;13(5):44-57. https://doi.org/10.15360/1813-9779-2017-5-44-57