Evaluation of possible neuroprotective effects of virgin coconut oil on aluminum-induced neurotoxicity in an in vitro Alzheimer's disease model

被引:4
|
作者
Demirel, Goksun [1 ,2 ]
Sanajou, Sonia [3 ]
Yirun, Anil [1 ,3 ]
Cakir, Deniz Arca [3 ,4 ]
Berkkan, Aysel [5 ]
Baydar, Terken [3 ]
Erkekoglu, Pinar [3 ,4 ]
机构
[1] Cukurova Univ, Fac Pharm, Dept Toxicol, Adana, Turkiye
[2] Cukurova Univ, Inst Addict & Forens Sci, Dept Forens Sci, Adana, Turkiye
[3] Hacettepe Univ, Fac Pharm, Dept Pharmaceut Toxicol, Ankara, Turkiye
[4] Hacettepe Univ, Vaccine Inst, Dept Vaccine Technol, Ankara, Turkiye
[5] Gazi Univ, Fac Pharm, Dept Analyt Chem, Ankara, Turkiye
关键词
aluminum; Alzheimer's disease; coconut oil; neurotransmitter; AMYLOID-BETA; ANTIOXIDANT CAPACITY; CORTICAL-NEURONS; DOPAMINE; RATS; NEUROBLASTOMA; INHIBITION; INCREASES; TOXICITY; EXPOSURE;
D O I
10.1002/jat.4564
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Alzheimer's disease (AD) is a progressive neurological disorder that affects various cognitive functions, behavior, and personality. AD is thought to be caused by a combination of genetic and environmental factors, including exposure to aluminum (Al). Virgin coconut oil (VCO) may have potential as a natural neuroprotectant against AD. Aim of this study was to determine neuroprotective effects of VCO on Al-induced neurotoxicity in an in vitro AD model. SH-SY5Y cells were initially cultured in normal growth medium and then differentiated by reducing fetal bovine serum content and adding retinoic acid (RA). Later, brain-derived neurotrophic factor (BDNF) was added along with RA. The differentiation process was completed on the seventh day. Study groups (n = 3) were designed as control group, VCO group, Al group, Al-VCO group, Alzheimer model (AD) group, AD + Al-exposed group (AD+Al), AD + VCO applied group (AD + VCO) and AD + Al-exposed + VCO applied group (AD + Al + VCO). Specific markers of AD (hyperphosphorylated Tau protein, amyloid beta 1-40 peptide, and amyloid precursor protein) were measured in all groups. In addition, oxidative stress parameters (total antioxidant capacity, lipid peroxidase, protein carbonyl, and reactive oxygen species) and neurotransmitter-related parameters (dopamine, dopamine transporter acetylcholine, and synuclein alpha levels, acetylcholinesterase activity) were measured comparatively in the study groups. VCO reduced amyloid beta and hyperphosphorylated Tau protein levels in the study groups. In addition, oxidative stress levels decreased, and neurotransmitter parameters improved with VCO. Our study shows that VCO may have potential therapeutic effects in Alzheimer's disease and further experiments are needed to determine its efficacy.
引用
收藏
页码:609 / 622
页数:14
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