The expression of NHE1 and apoptosis related protein in brain tissue of patients with lateral temporal lobe epilepsy

Wu Xuling, Dong Lian, Peng Shuang, Ye Lan, Xu Zucai, Feng Zhanhui

Chinese Journal of Clinical Anatomy ›› 2021, Vol. 39 ›› Issue (4) : 431-436.

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Chinese Journal of Clinical Anatomy ›› 2021, Vol. 39 ›› Issue (4) : 431-436. DOI: 10.13418/j.issn.1001-165x.2021.04.013

The expression of NHE1 and apoptosis related protein in brain tissue of patients with lateral temporal lobe epilepsy

  • Wu Xuling1,Dong Lian1,Peng Shuang1, Ye Lan2, Xu Zucai3,Feng Zhanhui1
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Abstract

Objective To detect the expression of Na+/H+ exchanger-1 (NHE1) and apoptosis related protein in brain tissue of patients with lateral temporal lobe epilepsy after operation and explore the pathogenic mechanism preliminarily. Methods Sixteen samples from patients with lateral temporal lobe epilepsy were collected as an epilepsy group, 10 samples from patients with temporal lobe tumor and cerebral hemorrhage as a control group. The pathological changes of brain tissue were observed by HE staining. The expression of NHE1 were further detected by immunohistochemistry and immunofluorescence. Western blot and other method was used to semi-quantitatively analyze the expression characteristics of NHE1, Bcl-2 and Bax. The data were collected and analyzed by SPSS 24.0 software. Results HE staining showed that neurons decreased, phagocytosis increased and microglia was hyperactive in the temporal lobe of the epilepsy  group. However, there was no similar expression in the control group. Immunofluorescence and immunohistochemical staining showed that NHE1 was located on neurons. NHE1 staining in the epilepsy group was significantly higher than that in the control group (P<0.05). The expression of NHE1 protein in the epilepsy group was significantly higher than that in the control group (P<0.05). The results of Bcl-2 and Bax showed that the expression of Bcl-2 in the epilepsy group was significantly lower than that in the control group (P<0.05), and the expression of Bax was significantly higher than that in the control group (P<0.05). Conclusions NHE1 is closely related to the formation and development of lateral temporal lobe epilepsy. The possible mechanism is closely related the increasing of NHE1 and neuron apoptosis.

Key words

Lateral temporal lobe epilepsy /  NHE1 /  Apoptosis /  Human brain tissue

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Wu Xuling, Dong Lian, Peng Shuang, Ye Lan, Xu Zucai, Feng Zhanhui. The expression of NHE1 and apoptosis related protein in brain tissue of patients with lateral temporal lobe epilepsy[J]. Chinese Journal of Clinical Anatomy. 2021, 39(4): 431-436 https://doi.org/10.13418/j.issn.1001-165x.2021.04.013

References

[1] Perucca P, Scheffer IE, Kiley M. The management of epilepsy in children and adults[J]. Med J Aust, 2018, 208(5): 226-233. DOI: 10.5694/mja17.00951.
[2]  Huberfeld G, Blauwblomme T, Miles R. Hippocampus and epilepsy: findings from human tissues[J]. Rev Neurol (Paris), 2015, 171(3): 236-251. DOI: 10.1016/j.neurol.2015.01.563.
[3]  Gataullina S, Dulac O, Bulteau C. Temporal lobe epilepsy in infants and children[J]. Rev Neurol (Paris), 2015, 171(3): 252-258. DOI: 10.1016/j.neurol.2015.01.559.
[4]  Aronica E, Mühlebner A. Neuropathology of epilepsy[J]. Handb Clin Neurol, 2017, 145(2): 193-216. DOI: 10.1016/B978-0-12-802395-2.00015-8.
[5] Fliegel L. Structural and functional changes in the Na+/H+ exchanger isoform 1, induced by Erk1/2 phosphorylation[J]. Int J Mol Sci, 2019, 20(10): 2378-2387. DOI: 10.3390/ijms20102378.
[6]  Kang TC, An SJ, Park SK, et al. Alterations in Na+/H+ exchanger and Na+ /HCO3- cotransporter immunoreactivities within the gerbil hippocampus following seizure[J]. Brain Res Mol Brain Res, 2002, 109(1-2): 226-232. DOI: 10.1016/s0169-328x(02)00559-4.
[7] Feng ZH, Hao JW, Ye L, et al. Overexpression of μ-calpain in the anterior temporal neocortex of patients with intractable epilepsy correlates with clinicopathological characteristic[J]. Seizure, 2011, 20(5): 395-401. DOI: 10.1016/j.seizure.2011.01.010.
[8]  冯占辉, 于云莉, 胡皓月, 等. m-钙蛋白酶在难治性癫痫患者脑组织的表达[J]. 癫痫与神经电生理学杂志, 2018, 27(2): 65-68.
[9] Gao H, Geng Z. Calpain I activity and its relationship with hippocampal neuronal death in pilocarpine-induced status epilepticus rat model[J]. Cell Biochem Biophys, 2013, 66(2): 371-377. DOI: 10.1007/s12013-012-9476-5.
[10]Feng ZH, Ye L, Klebe D, et al. Anti-inflammation conferred by stimulation of CD200R1 via Dok1 pathway in rat microglia after germinal matrix hemorrhage[J]. J Cereb Blood Flow Metab, 2019, 39(1): 97-107. DOI: 10.1177/0271678X17725211.
[11] Blumcke I, Spreafico R, Haaker G, et al. Histopathological findings in brain tissue obtained during epilepsy surgery[J]. N Engl J Med, 2017, 377(17): 1648-1656. DOI: 10.1056/NEJMoa1703784.
[12] Spasov AA, Gurova NA, Kharitonova MV. Structure and physiological role of NHE1 and pharmacological regulation of its activity[J]. Eksp Klin Farmakol, 2013, 76(1): 43-48. PMID: 23461016.
[13] Mendoza-Ferreira N, Coutelier M, Janzen E, et al. Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function[J]. Neurol Genet, 2018, 4(1): e209-e218. DOI: 10.1212/NXG.0000000000000209.
[14] Pelin C, Douglas BK, Chanana V, et al. Sustained Na+/H+ exchanger activation promotes gliotransmitter release from reactive hippocampal astrocytes following oxygen-glucose deprivation[J]. PLoS One, 2014, 9(1): e84294-e84302. DOI: 10.1371/journal.pone.0084294.
[15] Miyata H. [Surgical pathology of adulthood epilepsy][J]. Brain Nerve, 2017, 69(10): 1091-1104. DOI: 10.11477/mf.1416200876. 
[16] Li QR, Han Y, Du JB, et al. Alterations of apoptosis and autophagy in developing brain of rats with epilepsy: changes in LC3, P62, Beclin-1 and Bcl-2 levels[J]. Neurosci Res, 2018, 130: 47-55. DOI: 10.1016/j.neures.2017.08.004.
[17] 胡皓月, 冯占辉. 钙激活中性蛋白酶和钠氢交换体1在癫痫所致神经元损害中的研究进展[J]. 癫痫与神经电生理学杂志, 2017, 26(6): 379-382.
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