| Literature DB >> 34758720 |
Tapan Behl1, Arpita Arora1, Aayush Sehgal1, Sukhbir Singh1, Neelam Sharma1, Saurabh Bhatia2,3, Ahmed Al-Harrasi3, Simona Bungau4, Ebrahim Mostafavi5,6.
Abstract
Diabetes mellitus is a major metabolic disorder that has now emerged as an epidemic, and it affects the brain through an array of pathways. Patients with diabetes mellitus can develop pathological changes in the brain, which eventually take the shape of mild cognitive impairment, which later progresses to Alzheimer's disease. A number of preclinical and clinical studies have demonstrated this fact, and molecular pathways, such as amyloidogenesis, oxidative stress, inflammation, and impaired insulin signaling, are found to be identical in diabetes mellitus and dementia. However, the critical player involved in the vicious cycle of diabetes mellitus and dementia is insulin, whose signaling, when impaired in diabetes mellitus (both type 1 and 2), leads to a decline in cognition, although other pathways are also essential contributors. Moreover, it is not only the case that patients with diabetes mellitus indicate cognitive decline at a later stage, but many patients with Alzheimer's disease also reflect symptoms of diabetes mellitus, thus creating a vicious cycle inculcating a web of complex molecular mechanisms and hence categorizing Alzheimer's disease as 'brain diabetes.' Thus, it is practical to suggest that anti-diabetic drugs are beneficial in Alzheimer's disease. However, only smaller trials have showcased positive outcomes mainly because of the late onset of therapy. Therefore, it is extremely important to develop more of such molecules that target insulin in patients with dementia along with such methods that diagnose impaired insulin signaling and the associated cognitive decline so that early therapy may be initiated and the progression of the disease can be prevented. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Alzheimer’s disease; diabetes mellitus; forkhead box o (FOXO); glycogen synthase kinase 3 beta (GSK3β); insulin resistance; metabolic disorder
Mesh:
Substances:
Year: 2022 PMID: 34758720 DOI: 10.2174/1871527320666211110115257
Source DB: PubMed Journal: CNS Neurol Disord Drug Targets ISSN: 1871-5273 Impact factor: 4.388