2021
DOI: 10.1016/j.ejphar.2021.173974
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Role of natural products for the treatment of Alzheimer's disease

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Cited by 87 publications
(56 citation statements)
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“…However, synthetic molecules are used as the supply for clinical trials. In preclinical studies, bryostatin-1 was found to improve memory and learning for prolonged periods, produce neuroprotective effects in transgenic mice with AD, inhibit phosphorylation of the tau protein by inhibiting the enzyme GSK3beta, prevent neuronal apoptosis, decrease amyloid-beta levels in the Tg 2576 mouse with AD, recover neurotrophic activity and loss of synapses, and improve synaptogenesis, recovering cognitive deficits [ 119 , 120 , 183 , 194 , 195 ].…”
Section: Remarks and Future Perspectivesmentioning
confidence: 99%
“…However, synthetic molecules are used as the supply for clinical trials. In preclinical studies, bryostatin-1 was found to improve memory and learning for prolonged periods, produce neuroprotective effects in transgenic mice with AD, inhibit phosphorylation of the tau protein by inhibiting the enzyme GSK3beta, prevent neuronal apoptosis, decrease amyloid-beta levels in the Tg 2576 mouse with AD, recover neurotrophic activity and loss of synapses, and improve synaptogenesis, recovering cognitive deficits [ 119 , 120 , 183 , 194 , 195 ].…”
Section: Remarks and Future Perspectivesmentioning
confidence: 99%
“…Compounds used for the treatment and prophylaxis of AD symptoms are mainly flavonoids and alkaloids. Galantamine, huperzine A, and curcumin are only a few of the natural compounds that have been documented and summarized as AChE inhibitors and memory-supporting elements [ 13 ]. Resveratrol, quercetin, and berberine are also considered to be protective contributors [ 14 ].…”
Section: Introductionmentioning
confidence: 99%
“…The DESI-MS image showed that the L-glutamine ( m / z = 145.06) levels in the hypothalamus and cerebellum (Cb) of the BChE KO mice were higher than that of the wild-type mice ( Figure 9 B,D; WT vs. homozygote, p = 0.0147; WT vs. heterozgote, p = 0.3721). The DESI-MS image also showed that the N-acetyl-L-aspartic acid ( m / z = 174.04) levels in the hippocampus (Hip), hypothalamus [ 39 ], cerebral cortex (CX), and cerebellum (Cb) of the BChE KO mice were higher than that of the wild-type mice ( Figure 9 C,E; WT vs. homozygote, p = 0.0047; WT vs. heterozgote, p = 0.0454). Our data suggested that BChE enzyme activity inhibition increased glutamine and N-acetyl-L-aspartic acid content in the mouse brain.…”
Section: Resultsmentioning
confidence: 99%
“…The ionization of substances in negative ion mode generally exists in the form of [M−H] − or [M+CI] − . L-glutamine and N-acetyl-L-aspartic acid play important roles in brain metabolism and function [39]. The DESI-MS image showed that the L-glutamine (m/z = 145.06) levels in the hypothalamus and cerebellum (Cb) of the BChE KO mice were higher than that of the wild-type mice (Figure 9B,D; WT vs. homozygote, p = 0.0147; WT vs. heterozgote, p = 0.3721).…”
Section: Inhibited Bche Enzyme Activity Increased Glutamine and N-acetyl-l-aspartic Acid Content In Mouse Brainmentioning
confidence: 99%