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Benzodiazepines in Alzheimer's disease: beneficial or detrimental effects
被引:22
作者:
Al-Kuraishy, Hayder M.
[1
]
Al-Gareeb, Ali, I
[1
]
Saad, Hebatallah M.
[2
]
Batiha, Gaber El-Saber
[3
]
机构:
[1] Al Mustansiriyah Univ, Coll Med, Med Fac, Dept Pharmacol Toxicol & Med, POB 14132, Baghdad, Iraq
[2] Matrouh Univ, Fac Vet Med, Dept Pathol, Marsa Matruh 51744, Egypt
[3] Damanhour Univ, Fac Vet Med, Dept Pharmacol & Therapeut, Damanhour 22511, Egypt
关键词:
Alzheimer's disease;
Gamma-aminobutyric acid;
Benzodiazepines;
Cognitive dysfunction;
GABA-A RECEPTORS;
INDUCED IMPAIRMENT;
AMYLOID-BETA;
PLASTICITY;
PROTEIN;
RISK;
DYSFUNCTION;
ASSOCIATION;
LORAZEPAM;
TOXICITY;
D O I:
10.1007/s10787-022-01099-4
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Dementia is considered a clinical syndrome characterized by cognitive dysfunction and memory loss. Alzheimer's disease (AD) is the most common type of dementia. AD is linked with the turbulence of diverse neurotransmitters including gamma-aminobutyric acid (GABA). Notably, GABA in the brain and cerebrospinal fluid was reduced in AD. Thus, allosteric modulation of the GABA effect by benzodiazepines (BDZs) may improve the clinical outcomes of AD patients. Therefore, the objective of the present review was to reveal the possible role of BDZs on the pathogenesis and clinical outcomes in AD patients. Though BDZs may adversely affect cognitive functions mainly in elderly patients, herein it was postulated that BDZs may have beneficial, neutral, or detrimental effects in AD. Taken together, there is strong controversy regarding the use of BDZs and the risk for the development of AD. Therefore, experimental, preclinical and clinical studies are critical to determine the potential protective or detrimental effects of BDZs on AD neuropathology.
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页码:221 / 230
页数:10
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