Alzheimer's Disease Pathogenesis-Core Concepts, Shifting Paradigms and Therapeutic Targets 2011
DOI: 10.5772/17682
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Insulin Resistance, Cognitive Impairment and Neurodegeneration: Roles of Nitrosamine Exposure, Diet and Lifestyles

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Cited by 3 publications
(4 citation statements)
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References 183 publications
(216 reference statements)
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“…Besides the direct consequences of brain metabolic dysfunction, insulin resistance reinforces the neurodegeneration cascade in exacerbating amyloid accumulation, neuronal loss, and synaptic disconnection 7 . Altogether, the aggregate data support the hypothesis that Alzheimer's is a metabolic disorder in which brain insulin deficiency and resistance are at the core, and therefore shares molecular, biochemical, and pathophysiological features with diseases such as Type I and Type II diabetes mellitus 4, 6, 33, 44, 45 . Consequently a role for insulin therapy is justified in correcting the metabolic dysfunction.…”
Section: Introductionsupporting
confidence: 70%
See 1 more Smart Citation
“…Besides the direct consequences of brain metabolic dysfunction, insulin resistance reinforces the neurodegeneration cascade in exacerbating amyloid accumulation, neuronal loss, and synaptic disconnection 7 . Altogether, the aggregate data support the hypothesis that Alzheimer's is a metabolic disorder in which brain insulin deficiency and resistance are at the core, and therefore shares molecular, biochemical, and pathophysiological features with diseases such as Type I and Type II diabetes mellitus 4, 6, 33, 44, 45 . Consequently a role for insulin therapy is justified in correcting the metabolic dysfunction.…”
Section: Introductionsupporting
confidence: 70%
“…The consistent findings were that, among individuals who had brain insulin resistance associated with MCI, early AD, or Type 2 diabetes mellitus, significant improvements in cognition, memory, attention and metabolic function occurred within a few months of treatment in the clinical trials 26, 41, 62, 63 . Mechanistically, in addition to the stimulatory effects on energy metabolism, insulin increases amyloid clearance from the brain 64 and it supports neuronal cytoskeletal and cholinergic functions 6, 9, 11 . Furthermore, enhanced insulin signaling inhibits the activity of kinases that promote tau hyperphosphorylation, and activates pathways that mediate synapse formation and neuronal plasticity 65 .…”
Section: Intranasal Insulin Therapymentioning
confidence: 99%
“…12,[30][31][32][33][34] The molecular and biochemical consequences of insulin resistance in the brain are caused due to impairments in the insulin signalling pathway that compromises neuronal survival, energy production, gene expression, plasticity and white matter integrity. 33,35,36 The brain undergoes a starvation state due to deficit in glucose uptake and utilization, thus causing oxidative stress, impairments in homeostasis and increased cell death. Impairments in insulin signalling results in neurodegeneration due to increased activity of kinases that aberrantly phosphorylates tau, generation of reactive oxygen species that damages proteins, nucleic acids and lipids, leads to accumulation of amyloid beta monomers and plaques, causes mitochondrial dysfunction and increase signalling through pro-inflammatory and pro-apoptosis cascades.…”
Section: Discussionmentioning
confidence: 99%
“…Impairments in insulin signalling results in neurodegeneration due to increased activity of kinases that aberrantly phosphorylates tau, generation of reactive oxygen species that damages proteins, nucleic acids and lipids, leads to accumulation of amyloid beta monomers and plaques, causes mitochondrial dysfunction and increase signalling through pro-inflammatory and pro-apoptosis cascades. [35][36][37][38] Also insulin resistance is associated with down-regulation of genes needed for cholinergic function, thereby further compromising neuronal plasticity, memory and cognition. 36,38 The basis of the neuroprotective effects of the test formulation is corroborated by several studies in animals and humans.…”
Section: Discussionmentioning
confidence: 99%