Neuroprotective effects of nobiletin and tangeretin against amyloid β1-42-induced toxicity in cultured primary rat neurons

被引:5
|
作者
Hung, Wei-Lun [1 ]
Chiu, Tsao-Hsiang [2 ]
Wei, Guor-Jien [3 ,4 ]
Pan, Min-Hsiung [2 ]
Ho, Chi-Tang [5 ]
Hwang, Lucy Sun [2 ]
Hsu, Bo-Yang [6 ,7 ]
机构
[1] Taipei Med Univ, Sch Food & Safety, Taipei 110, Taiwan
[2] Natl Taiwan Univ, Grad Inst Food Sci & Technol, Taipei 106, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Inst Food Safety & Hlth Risk Assessment, Taipei 112, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Metab Prote Res Ctr, Taipei 112, Taiwan
[5] Rutgers State Univ, Dept Food Sci, New Brunswick, NJ 08901 USA
[6] Natl Ilan Univ, Dept Food Sci, Yilan 260, Yilan, Taiwan
[7] Lee Ming Inst Technol, Dept Food & Beverage Management, New Taipei City 243, Taiwan
关键词
Alzheimer's disease; Neuroprotective effects; Nobiletin; Tangeretin; BETA; AGGREGATION; NEUROTOXICITY; IMPAIRMENT; MODEL;
D O I
10.1186/s41110-023-00241-8
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Background Amyloid beta (A beta)-induced oxidative stress and neurotoxicity play an important role in the pathogenesis of Alzheimer's disease (AD). In this study, we evaluated the neuroprotective effects of nobiletin and tangeretin against A beta-induced neurotoxicity in primary rat neurons. Methods The protection of nobiletin and tangeretin against A beta(1-42) toxicity on primary cortical neurons was determined by the MTT assay. The free radical scavenging ability of nobiletin and tangeretin was evaluated by measuring the intensity of dichlorodihydrofluorescein (DCF) fluorescence. The protective effects of nobiletin and tangeretin against A beta(1-42)-induced neurotoxicity were further evaluated by the western blot and thioflavin T binding assay. Results Nobiletin (1, 5, 12.5, 25, 50 mu M) and tangeretin (1, 5, 12.5, 25 mu M) significantly decreased A beta-induced neurotoxicity in a concentration-dependent manner (P < 0.05 or P < 0.01). The cell viability of neuronal cells decreased to 68.5% by treatment of A beta(1-42) (1 mu M). The highest cell viability (81.4%) of nobiletin treatment group was found at the concentration of 50 mu M. Meanwhile, tangeretin possessed the highest neuroprotective effect at the concentration of 25 mu M in which the cell viability was 88.9%. In addition, nobiletin and tangeretin effectively suppressed A beta-induced intracellular oxidative stress (P < 0.05). Tangeretin also significantly reduced the aggregation of A beta(1-42) monomer (P < 0.01), while aggregation of A beta(1-42) was not significantly inhibited by treatment with nobiletin. Conclusion Both nobiletin and tangeretin significantly decreased A beta(1-42)-induced neurotoxicity. Tangeretin significantly reduced the aggregation of A beta(1-42), while the neuroprotective effect of nobiletin was due to the reduction of oxidative damage. The results suggested that tangeretin and nobiletin might be a potential neuroprotective food ingredient.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] Neuroprotective effects of INT-777 against Aβ1-42-induced cognitive impairment, neuroinflammation, apoptosis, and synaptic dysfunction in mice
    Wu, Xian
    Lv, Yang-Ge
    Du, Yi-Feng
    Chen, Fang
    Reed, Miranda N.
    Hu, Mei
    Suppiramaniam, Vishnu
    Tang, Su-Su
    Hong, Hao
    BRAIN BEHAVIOR AND IMMUNITY, 2018, 73 : 533 - 545
  • [32] Neuroprotective effect of ropinirole against Aβ1-42-induced neurochemical perturbations and cognitive impairments in a rodent model
    Akram, Mohd.
    Neha, Mohd
    Pinky, Mohd
    Saqib, Mohd
    Salman, Mohd
    Parvez, Suhel
    KAOHSIUNG JOURNAL OF MEDICAL SCIENCES, 2023, 39 (11): : 1119 - 1128
  • [33] Role of amber extract in protecting SHSY5Y cells against amyloid β1-42-induced neurotoxicity
    Luo, Yuening
    Zhou, Siqi
    Haeiwa, Haruna
    Takeda, Reiko
    Okazaki, Kazuma
    Sekita, Marie
    Yamamoto, Takuya
    Yamano, Mikio
    Sakamoto, Kazuichi
    BIOMEDICINE & PHARMACOTHERAPY, 2021, 141
  • [34] Idebenone protects mitochondrial function against amyloid beta toxicity in primary cultured cortical neurons
    Wang, Huiting
    Li, Lei
    Jia, Kun
    Wang, Qi
    Sui, Shaomei
    Lin, Yicheng
    He, Yan
    NEUROREPORT, 2020, 31 (15) : 1104 - 1110
  • [35] Chitosan oligosaccharides alleviate cognitive deficits in an amyloid-β1-42-induced rat model of Alzheimer's disease
    Jia, Shiliang
    Lu, Zheng
    Gao, Zhaolan
    An, Jun
    Wu, Xueling
    Li, Xiaoxiao
    Dai, Xueling
    Zheng, Qiusheng
    Sun, Yaxuan
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2016, 83 : 416 - 425
  • [36] 1,5-dicaffeoylquinic acid protects primary neurons from amyloid β1-42-induced apoptosis via PI3K/Akt signaling pathway
    Xiao Hai-bing
    Cao Xu
    Wang Lei
    Run Xiao-qin
    Su Ying
    Tian Cheng
    Sun Sheng-gang
    Liang Zhi-hou
    CHINESE MEDICAL JOURNAL, 2011, 124 (17) : 2628 - 2635
  • [37] The Protective Effects of Crocetin on Aβ1-42-Induced Toxicity in Ht22 Cells
    Kong, Yan
    Kong, Ling-Ping
    Luo, Tao
    Li, Guang-Wu
    Jiang, Wei
    Li, Sheng
    Zhou, Yue
    Wang, Hua-Qiao
    CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2014, 13 (09) : 1627 - 1632
  • [38] The protective effects of Chromofungin in oligomeric amyloid β42 (Aβ42)-induced toxicity in neurons in Alzheimer's disease
    Li, Qingwei
    Sun, Ji
    Ran, Qin
    Liu, Ziming
    Chen, Jinmei
    AGING-US, 2024, 16 (10): : 9216 - 9227
  • [39] Involvement of Intracellular and Mitochondrial Aβ in the Ameliorative Effects of Huperzine A against Oligomeric Aβ42-Induced Injury in Primary Rat Neurons
    Lei, Yun
    Yang, Ling
    Ye, Chun Yan
    Qin, Ming Yan
    Yang, Huai Yu
    Jiang, Hua Liang
    Tang, Xi Can
    Zhang, Hai Yan
    PLOS ONE, 2015, 10 (05):
  • [40] The Effect of Ghrelin on Apoptosis, Necroptosis and Autophagy Programmed Cell Death Pathways in the Hippocampal Neurons of Amyloid-β 1-42-Induced Rat Model of Alzheimer's Disease
    Naseri, Faezeh
    Sirati-Sabet, Majid
    Sarlaki, Fatemeh
    Keimasi, Mohammad
    Mokarram, Poneh
    Siri, Morvarid
    Ghasemi, Rasoul
    Shahsavari, Zahra
    Goshadrou, Fatemeh
    INTERNATIONAL JOURNAL OF PEPTIDE RESEARCH AND THERAPEUTICS, 2022, 28 (05)