DOI QR코드

DOI QR Code

Neuroprotective Effects of Kaempferol, Quercetin, and Its Glycosides by Regulation of Apoptosis

Kaempferol, quercetin 및 그 배당체들의 apoptosis 조절을 통한 신경세포 보호 효과

  • Kim, Ji Hyun (Department of Food Science and Nutrition, Pusan National University) ;
  • Lee, Sanghyun (Department of Integrative Plant Science, Chung-Ang University) ;
  • Cho, Eun Ju (Department of Food Science and Nutrition, Pusan National University) ;
  • Kim, Hyun Young (Department of Food Science, Gyeongnam National University of Science and Technology)
  • 김지현 (부산대학교 식품영양학과) ;
  • 이상현 (중앙대학교 식물시스템과학과) ;
  • 조은주 (부산대학교 식품영양학과) ;
  • 김현영 (경남과학기술대학교 식품과학부)
  • Received : 2018.11.06
  • Accepted : 2019.02.01
  • Published : 2019.02.28

Abstract

Alzheimer's disease (AD) is a neurodegenerative disease caused by accumulation of amyloid beta ($A{\beta}$) in the brain. In the present study, we investigated the neuroprotective effects of four flavonoids such as kaempferol, kaempferol-3-O-glucoside, quercetin, and quercetin-3-${\beta}$-D-glucoside against neuronal apoptosis induced by $A{\beta}$ in SH-SY5Y neuronal cells. Treatment with $A{\beta}$ decreased cell viability compared to the non-treated normal group. However, treatment with the four flavonoids increased cell viability in SH-SY5Y cells treated with $A{\beta}$. In addition, we measured the expression of apoptosis-related proteins such as Bcl-2-associated X protein (Bax) and cleaved caspase-9. Treatment with the four flavonoids down-regulated Bax and cleaved caspase-9 in $A{\beta}$-treated SH-SY5Y neuronal cells. Overall, the results of the present study demonstrated the neuroprotective effect of flavonoids by anti-apoptotic activity in $A{\beta}$-induced SH-SY5Y neuronal cells. These results suggest that these four flavonoids would be useful therapeutic and prevention agents for AD.

알츠하이머 질환은 대표적인 신경퇴행성 질환으로, 뇌 내에서 $A{\beta}$ 단백질 축적은 알츠하이머 질환의 원인으로 알려져 있다. 본 연구에서는 amyloid beta ($A{\beta}$)로 손상을 유도한 SH-SY5Y 신경세포에서 kaempferol, kaempferol-3-O-glucoside, quercetin, quercetin-3-${\beta}$-D-glucoside의 신경세포 보호 효과에 대해 검토하였다. SH-SY5Y 신경세포에 $A{\beta}_{25-35}$ ($25{\mu}M$)를 처리하였을 때, 처리하지 않은 normal군에 비해 세포생존율이 유의적으로 감소하였다. 반면, kaempferol, quercetin 및 그 배당체들을 각각 처리하였을 때 $A{\beta}_{25-35}$만을 처리한 control군에 비해 유의적으로 세포생존율의 증가를 나타내었다. 또한, apoptosis에 관여하는 cleaved caspase9, Bcl-2-associated X protein (Bax) 단백질 발현을 측정한 결과, normal군에 비해 control군에서 유의적으로 cleaved caspase9 및 Bax 단백질 발현의 증가를 나타내어 $A{\beta}$ 유도 신경세포 손상으로 인한 apoptosis가 유발됨을 확인 하였으며, kaempferol, quercetin 및 그 배당체들의 처리 시 apoptosis 관련 단백질 발현이 감소함으로써 신경세포 보호 효능이 나타냄을 확인하였다. 이러한 결과는 kaempferol, quercetin 및 그 배당체들이 apoptosis 조절을 통해 신경세포 보호 효과를 나타내며, 신경세포 손상으로 인한 알츠하이머 질환을 예방하는 유용한 소재로써 사용 가능성이 있음을 보여준다.

Keywords

SHGSCZ_2019_v20n2_286_f0001.png 이미지

Fig. 1. Chemical structure of kaempferol (A), kaempferol -3-O-glucoside (B), quercetin (C), quercetin-3-β -D-glucoside (D)

SHGSCZ_2019_v20n2_286_f0002.png 이미지

Fig. 2. Effect of kaempferol (K), kaempferol-3-O-glucoside (KG), quercetin (Q), and quercetin-3-β-D-glucoside(QG) on apoptosis-related protein expression in SH-SY5Y cells treated with Aβ25-35. Values are mean ± SD. a~dMeans with the different letters are significantly different (P<0.05) by Duncan’s multiple range test. N:normal group; C:control group; K:kaempferol; KG:kaempferol-3-O-glucoside

Table 1. Effect of kaempferol, quercetin and its glycosides on cell viability of SH-SY5Y cells treated with Aβ25-35

SHGSCZ_2019_v20n2_286_t0001.png 이미지

References

  1. D. L. Bachman, P. A. wolf, R. T. Linn, J. E. Knoefel, J. L. Cobb, A. J. Belanger, L. R. White, R. B. D'Agostino. "Incidence of dementia and probable Alzheimers disease in a general population: the Framingham Study.", Neurology, Vol.43, No.3 Pt 1 pp.515-519, 1993. DOI: http://dx.doi.org/10.1212/WNL.43.3_Part_1.515
  2. D. J. Selkoe. "Alzheimer's disease: a central role for amyloid.", Journal of Neuropathology & Experimental Neurology, Vol.53, No.5 pp.437-447, 1994. DOI: https://doi.org/10.1097/00005072-199409000-00003
  3. A. Nunomura, R. J. Castellani, X. Zhu, P. I. Moreira, G. Perry, M. A. Smith. "Involvement of oxidative stress in Alzheimer disease.", Journal of Neuropathology & Experimental Neurology, Vol.65, No.7 pp.631-641, 2006. DOI: https://dx.doi.org/10.1097/01.jnen.0000228136.58062.bf
  4. M. Vila, S. Przedborski. "Targeting programmed cell death in neurodegenerative diseases.", Nature Reviews Neuroscience, Vol.4, No.5 pp.365-375, 2003. DOI: https://dx.doi.org/10.1038/nrn1100
  5. H. Badshah, T. H. Kim, M. O. Kim. "Protective effects of anthocyanins against amyloid beta-induced neurotoxicity in vivo and in vitro.", Neurochemistry International, Vol.80 pp.51-59, 2015. DOI: https://dx.doi.org/10.1016/j.neuint.2014.10.009
  6. D. Y. Choi, Y. J. Lee, J. T. Hong, H. J. Lee. "Antioxidant properties of natual polyphenols and their therapeutic potentials for Alzheimers disease." Brain Research Bulletin, Vol.87, No.2-3 pp.144-153, 2012. DOI:https://dx.doi.org/10.1016/j.brainresbull.2011.11.014
  7. G. B. Gonzales, K. Raes, S. Coelus, K. Struijs, G. Smagghe, J. Van Camp. "Ultra(high)-pressure liquid chromatography-electrospray ionization-time-of-flight-ion mobility-high definition mass spectrometry for the rapid identification and structural characterization of flavonoid glycosides from cauliflower waste.", Journal of Chromatography, Vol.1323 pp.39-48, 2014. DOI: https://dx.doi.org/10.1016/j.chroma.2013.10.077
  8. D. G. Lee, K. H. Lee, K. W. Park, C. K. Han, B. Y. Ryu, E. J. Cho, S. Lee. "Isolation and identification of flavonoids with aldose reductase inhibitory activity from Petasites japonicus.", Asian Journal of Chemisty, Vol.27, No.3 pp.991-994, 2015. DOI: https://dx.doi.org/10.14233/ajchem.2015.17845
  9. J. W. Kang, J. H. Kim, K. Song, S. H. Kim, J. H. Yoon, K. S. Kim. "Kaempferol and quercetin, components of Ginkgo biloba extract (EGb 761), induced caspase-3-dependent apoptosis in oral cavity cancer cells.", Phytotherapy Research, Vol.24, No.1 pp.S77-82, 2010. DOI: https://dx.doi.org/10.1002/ptr.2913
  10. A. Roth, W. Schaffner, C. Hertel. "Phytoestrogen kampferol (3,4',5,7-tetrahydroxyflavone) protects PC12 and T47D cells from beta-amyloid-induced toxicity.", Journal of Neuroscience Research, Vol.57, No.3 pp.399-404, 1999. DOI: https://doi.org/10.1002/(SICI)1097-4547(19990801) 57:3<399::AID-JNR12>3.0.CO;2-W
  11. L. Yu, C. Chen, L. F. Wang, X. Kuang, K. Liu, H. Zhang, J. R. Du. "Neuroprotective effect of kaempferol glycosides against brain injury and neuroinflammation by inhibiting the activation of NF-${\kappa}B$ and STAT3 in transient focal stroke.", Plos One, Vol.8, No.2 pp.e55839, 2013. DOI: https://doi.org/10.1371/journal.pone.0055839
  12. A. M. Sabogal-Guaqueta, J. I. Munoz-Manco, J. R. Ramirez-Pineda, M. Lamprea-Rodriguez, E. Osorio, G. P. Cardona-Gomez. "The flavonoid quercetin ameliorates Alzheimers disease pathology and protects cogntiive and emotional function in aged triple transgenic Alzheimers disease model mice.", Neuropharmacology. Vol.93 pp.134-145, 2015. DOI: https://doi.org/10.1016/j.neuropharm.2015.01.027
  13. Y. Li, S. Zhow, J. Li, Y. Sun, H. Hasimu, R. Liu, T. Zhang. "Quercetin protects human brain microvascular endothelial cells from fibrillar ${\beta}$-amyloid1-40-induced toxocity.", Acta Pharmaceutica Sinica B, Vol.5, No.1 pp.47-54, 2015. DOI: https://doi.org/10.1016/j.apsb.2014.12.003
  14. M. A. Ansari, H. M. Abdul, G. Joshi, W. O. Opii, D. A. Butterfield. "Protective effect of quercetin in primary neurons against Abeta(1-42): relevance to Alzheimers disease.", Journal of Nutritional Biochemistry, Vol.20, No.4 pp.269-275, 2009. DOI: https://doi.org/10.1016/j.jnutbio.2008.03.002
  15. R. Soundararajan, A. D. Wishart, H. P. Rupasinghe, M Arcellana-Panlilio, C. M. Nelson, M. Mayne, G. X. Robertson. "Quercetin 3-glucoside protects neuroblastoma (SH-SY5Y) cells in vitro against oxidative damage by inducing sterol regulatory element-binding protein-2-mediated cholesterol biosynthesis.", Journal of Biological Chemistry, Vol.283, No.4 pp.2231-2245, 2008. DOI: https://doi.org/10.1074/jbc.M703583200
  16. T. Mosmann. "Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays.", Journal of Immunological Methods, Vol.65, No.1-2 pp.55-63, 1983. DOI: https://doi.org/10.1016/0022-1759(83)90303-4
  17. Y. Yamaguchi, S. Kawashima. "Effects of amyloid-beta-(25-35) on passive avoidance, radial-arm maze learning and choline acetyltransferase activity in the rat.", European Journal of Pharmacology, Vol.412, No.3 pp.265-272, 2001. DOI: https://doi.org/10.1016/S0014-2999(01)00730-0
  18. D. T. Loo, A. Copani, C. J. Pike, E. R. Whittemore, A. J. Walencewicz, C. W. Cotman. "Apoptosis is induced by beta-amyloid in cultured central nervous system neurons.", Proceedings of the National Academy of Sciences U S A, Vol.90, No.17 pp.7951-7955, 1993. DOI: https://doi.org/10.1073/pnas.90.17.7951
  19. A. Takahashi, A. Masuda, M. Sun, V. E. Centonze, B. Herman. "Oxidative stress-induced apoptosis is associated with alterations in mitochondrial caspase activity and Bcl-2-dependent alterations in mitochondrial pH (pHm).", Brain Research Bulletin, Vol.62, No.6 pp.497-504, 2004. DOI: https://dx.doi.org/10.1016/j.brainresbull.2003.07.009
  20. N. A. Abramova, D. S. Cassarino, S. M. Khan, T. W. Painter, J. P. Bennett Jr. "Inhibition by R(+) or S(-) pramipexole of caspase activation and cell death induced by methylpyridinium ion or beta amyloid peptide in SH-SY5Y neuroblastoma.", Journal of Neuroscience Research, Vol.67, No.4 pp.494-500, 2002. DOI: https://dx.doi.org/10.1002/jnr.10127
  21. S. Thummayot, C. Tocharus, D. Pinkaew, K. Viwatpinyo, K. Sringarm, J. Tocharus. Neuroprotective effect of purple rice extract and its constituent against amyloid beta-induced neuronal cell death in SK-N-SH cells. Neurotoxicology, Vol.45 pp.149-158, 2014. DOI: https://dx.doi.org/10.1016/j.neuro.2014.10.010
  22. C. N. Wang, C. W. Chi, Y. L. Lin, C. F. Chen, Y. J. Shiao. "The neuroprotective effects of phytoestrogens on amyloid beta protein-induced toxicity are mediated by abrogating the activation of caspase cascade in rat cortical neurons.", Journal of Biological Chemistry, Vol.276, No.7 pp.5287-5295, 2001. DOI: https://dx.doi.org/10.1074/jbc.M006406200
  23. K. M. Pate, M. Rogers, J. W. Reed, N. M. Van Der, S. Z. Vance, M. A. Moss. "Anthoxanthin polyphenols attenuate Aβ oligomer-induced neuronal responses associated with Alzheimer's disease.", CNS Neuroscience & Therapeutics, Vol.23, No.2 pp.135-144, 2017. DOI: https://dx.doi.org/10.1111/cns.12659
  24. P. Khaengkhan, Y. Nishikaze, T. Niidome, K. Kanaori, K. Tajima, M. Ichida, S. Harada, H. Sugimoto, K. Kamei. "Identification of an antiamyloidogenic substance from mulberry leaves.", NeuroReport, Vol.20, No.13 pp.1214-1218, 2009. DOI: https://dx.doi.org/10.1097/WNR.0b013e32832fa645
  25. C. Shi, L. Zhao, B. Zhu, Q. Li, D. T. Yew, Z. Yao, J. Xu. "Protective effects of Ginkgo biloba extract (EGb761) and its constituents quercetin and ginkgolide B against beta-amyloid peptide-induced toxicity in SH-SY5Y cells.", Chemistry Biological Interactions, Vol.181, No.1 pp.115-123, 2009. DOI: https://dx.doi.org/10.1016/j.cbi.2009.05.010
  26. M. A. Ansari, H. M. Abdul, G. Joshi, W. O. Opii, D. A. Butterfield. "Protective effect of quercetin in primary neurons against Abeta(1-42): relevance to Alzheimer's disease.", The Journal of Nutritional Biochemisty, Vol.20, No.4 pp.267-275, 2009. DOI: https://dx.doi.org/10.1016/j.jnutbio.2008.03.002
  27. Y. Dai, H. Zhang, J. Zhang, M. Yan. "Isoquercetin attenuates oxidative stress and neuronal apoptosis after ischemia/reperfusion injury via Nrf2-mediated inhibition of the NOX4/ROS/NF-kB pathway.". Chemico-Biological Interactions, Vol.284 pp.32-40, 2018. DOI: https://dx.doi.org/10.1016/j.cbi.2018.02.017