Herbal Treatments for ECS-Induced Memory Deficits: A Review of Research and a Discussion on Animal Models

2000 ◽  
Vol 16 (2) ◽  
pp. 144-156 ◽  
Author(s):  
Chittaranjan Andrade ◽  
S. Sudha ◽  
B. V. Venkataraman
Author(s):  
Angela K. Hochhalter ◽  
Whitney A. Sweeney ◽  
Lisa M. Savage ◽  
Bruce L. Bakke ◽  
J. Bruce Overmier

2004 ◽  
Vol 6 (4) ◽  
pp. 369-377 ◽  

Mild cognitive impairment (MCI) is an aspect of cognitive aging that is considered to be a transitional state between normal aging and the dementia into which it may convert. Appropriate animal models are necessary in order to understand the pathogenic mechanisms of MCI and develop drugs for its treatment. In this review, we identify the features that should characterize an animal model of MCI, namely old age, subtle memory impairment, mild neuropathological changes, and changes in the cholinergic system, and the age at which these features can be detected in laboratory animals. These features should occur in aging animals with normal motor activity and feeding behavior. The animal models may be middle-aged rats and mice, rats with brain ischemia, transgenic mice overexpressing amyloid precursor protein and presenilin 1 (tested at an early stage), or aging monkeys. Memory deficits can be detected by selecting appropriately difficult behavioral tasks, and the deficits can be associated with neuropathological alterations. The reviewed literature demonstrates that, under certain conditions, these animal species can be considered to be MCI models, and that cognitive impairment in these models responds to drug treatment.


2018 ◽  
Vol 45 (5) ◽  
pp. 237-246 ◽  
Author(s):  
Weiwei Ma ◽  
Mengnan Wu ◽  
Siyan Zhou ◽  
Ye Tao ◽  
Zuolei Xie ◽  
...  

2005 ◽  
Vol 5 (4) ◽  
pp. 122-126 ◽  
Author(s):  
Tetsu NAGATA ◽  
Satoshi YAMAMOTO ◽  
Takahiro YAGUCHI ◽  
Hiroyuki ISO ◽  
Akito TANAKA ◽  
...  

2020 ◽  
Vol 26 (15) ◽  
pp. 1693-1711 ◽  
Author(s):  
Alaa Alachkar ◽  
Shreesh K. Ojha ◽  
Adel Sadeq ◽  
Abdu Adem ◽  
Annika Frank ◽  
...  

: Epilepsy is a chronic neurological disorder characterized by irregular, excessive neuronal excitability, and recurrent seizures that affect millions of patients worldwide. Currently, accessible antiepileptic drugs (AEDs) do not adequately support all epilepsy patients, with around 30% patients not responding to the existing therapies. As lifelong epilepsy treatment is essential, the search for new and more effective AEDs with an enhanced safety profile is a significant therapeutic goal. Seizures are a combination of electrical and behavioral events that can induce biochemical, molecular, and anatomic changes. Therefore, appropriate animal models are required to evaluate novel potential AEDs. Among the large number of available animal models of seizures, the acute pentylenetetrazole (PTZ)-induced myoclonic seizure model is the most widely used model assessing the anticonvulsant effect of prospective AEDs, whereas chronic PTZ-kindled seizure models represent chronic models in which the repeated administration of PTZ at subconvulsive doses leads to the intensification of seizure activity or enhanced seizure susceptibility similar to that in human epilepsy. In this review, we summarized the memory deficits accompanying acute or chronic PTZ seizure models and how these deficits were evaluated applying several behavioral animal models. Furthermore, major advantages and limitations of the PTZ seizure models in the discovery of new AEDs were highlighted. With a focus on PTZ seizures, the major biochemicals, as well as morphological alterations and the modulated brain neurotransmitter levels associated with memory deficits have been illustrated. Moreover, numerous medicinal compounds with concurrent anticonvulsant, procognitive, antioxidant effects, modulating effects on several brain neurotransmitters in rodents, and several newly developed classes of compounds applying computer-aided drug design (CADD) have been under development as potential AEDs. The article details the in-silico approach following CADD, which can be utilized for generating libraries of novel compounds for AED discovery. Additionally, in vivo studies could be useful in demonstrating efficacy, safety, and novel mode of action of AEDs for further clinical development.


Nutrients ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1942 ◽  
Author(s):  
Wei Wang ◽  
Daisuke Tanokashira ◽  
Yusuke Fukui ◽  
Megumi Maruyama ◽  
Chiemi Kuroiwa ◽  
...  

The biological effects of insulin signaling are regulated by the phosphorylation of insulin receptor substrate 1 (IRS1) at serine (Ser) residues. In the brain, phosphorylation of IRS1 at specific Ser sites increases in patients with Alzheimer’s disease (AD) and its animal models. However, whether the activation of Ser sites on neural IRS1 is related to any type of memory decline remains unclear. Here, we show the modifications of IRS1 through its phosphorylation at etiology-specific Ser sites in various animal models of memory decline, such as diabetic, aged, and amyloid precursor protein (APP) knock-in NL-G-F (APPKINL-G-F) mice. Substantial phosphorylation of IRS1 at specific Ser sites occurs in type 2 diabetes- or age-related memory deficits independently of amyloid-β (Aβ). Furthermore, we present the first evidence that, in APPKINL-G-F mice showing Aβ42 elevation, the increased phosphorylation of IRS1 at multiple Ser sites occurs without memory impairment. Our findings suggest that the phosphorylation of IRS1 at specific Ser sites is a potential marker of Aβ-unrelated memory deficits caused by type 2 diabetes and aging; however, in Aβ-related memory decline, the modifications of IRS1 may be a marker of early detection of Aβ42 elevation prior to the onset of memory decline in AD.


2019 ◽  
Vol 10 (10) ◽  
pp. 745-759 ◽  
Author(s):  
Wenjuan Wu ◽  
Shuwen Du ◽  
Wei Shi ◽  
Yunlong Liu ◽  
Ying Hu ◽  
...  

2019 ◽  
Vol 42 ◽  
Author(s):  
Nicole M. Baran

AbstractReductionist thinking in neuroscience is manifest in the widespread use of animal models of neuropsychiatric disorders. Broader investigations of diverse behaviors in non-model organisms and longer-term study of the mechanisms of plasticity will yield fundamental insights into the neurobiological, developmental, genetic, and environmental factors contributing to the “massively multifactorial system networks” which go awry in mental disorders.


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