Metformin a Potential Pharmacological Strategy in Late Onset Alzheimer's Disease Treatment.
Saghar Rabiei PoorMiren EtchettoAmanda CanoElena Sánchez-LopezPatricia Regina ManzineJordi OlloquequiAntonio Camins EspunyMohammad JavanPublished in: Pharmaceuticals (Basel, Switzerland) (2021)
Alzheimer's disease (AD) is one of the most devastating brain disorders. Currently, there are no effective treatments to stop the disease progression and it is becoming a major public health concern. Several risk factors are involved in the progression of AD, modifying neuronal circuits and brain cognition, and eventually leading to neuronal death. Among them, obesity and type 2 diabetes mellitus (T2DM) have attracted increasing attention, since brain insulin resistance can contribute to neurodegeneration. Consequently, AD has been referred to "type 3 diabetes" and antidiabetic medications such as intranasal insulin, glitazones, metformin or liraglutide are being tested as possible alternatives. Metformin, a first line antihyperglycemic medication, is a 5'-adenosine monophosphate (AMP)-activated protein kinase (AMPK) activator hypothesized to act as a geroprotective agent. However, studies on its association with age-related cognitive decline have shown controversial results with positive and negative findings. In spite of this, metformin shows positive benefits such as anti-inflammatory effects, accelerated neurogenesis, strengthened memory, and prolonged life expectancy. Moreover, it has been recently demonstrated that metformin enhances synaptophysin, sirtuin-1, AMPK, and brain-derived neuronal factor (BDNF) immunoreactivity, which are essential markers of plasticity. The present review discusses the numerous studies which have explored (1) the neuropathological hallmarks of AD, (2) association of type 2 diabetes with AD, and (3) the potential therapeutic effects of metformin on AD and preclinical models.
Keyphrases
- cognitive decline
- type diabetes
- cerebral ischemia
- protein kinase
- insulin resistance
- white matter
- late onset
- resting state
- glycemic control
- public health
- mild cognitive impairment
- risk factors
- skeletal muscle
- functional connectivity
- subarachnoid hemorrhage
- working memory
- early onset
- blood brain barrier
- cardiovascular disease
- healthcare
- emergency department
- multiple sclerosis
- stem cells
- body mass index
- physical activity
- human health
- risk assessment
- climate change
- adverse drug
- replacement therapy
- drug induced