Bio-Hacking Better Health-Leveraging Metabolic Biochemistry to Maximise Healthspan.
Isabella D CooperYvoni KyriakidouLucy PetagineKurtis EdwardsBradley T ElliottPublished in: Antioxidants (Basel, Switzerland) (2023)
In the pursuit of longevity and healthspan, we are challenged with first overcoming chronic diseases of ageing: cardiovascular disease, hypertension, cancer, dementias, type 2 diabetes mellitus. These are hyperinsulinaemia diseases presented in different tissue types. Hyperinsulinaemia reduces endogenous antioxidants, via increased consumption and reduced synthesis. Hyperinsulinaemia enforces glucose fuelling, consuming 4 NAD + to produce 2 acetyl moieties; beta-oxidation, ketolysis and acetoacetate consume 2, 1 and 0, respectively. This decreases sirtuin, PARPs and oxidative management capacity, leaving reactive oxygen species to diffuse to the cytosol, upregulating aerobic glycolysis, NF-kB and cell division signalling. Also, oxidising cardiolipin, reducing oxidative phosphorylation (OXPHOS) and apoptosis ability; driving a tumourigenic phenotype. Over time, increasing senescent/pathological cell populations occurs, increasing morbidity and mortality. Beta-hydroxybutyrate, an antioxidant, metabolite and signalling molecule, increases synthesis of antioxidants via preserving NAD + availability and enhancing OXPHOS capacity. Fasting and ketogenic diets increase ketogenesis concurrently decreasing insulin secretion and demand; hyperinsulinaemia inhibits ketogenesis. Lifestyles that maintain lower insulin levels decrease antioxidant catabolism, additionally increasing their synthesis, improving oxidative stress management and mitochondrial function and, subsequently, producing healthier cells. This supports tissue and organ health, leading to a better healthspan, the first challenge that must be overcome in the pursuit of youthful longevity.
Keyphrases
- oxidative stress
- induced apoptosis
- cardiovascular disease
- cell cycle arrest
- healthcare
- public health
- reactive oxygen species
- type diabetes
- single cell
- cell therapy
- diabetic rats
- mental health
- dna damage
- blood pressure
- cell death
- blood glucose
- glycemic control
- signaling pathway
- health information
- insulin resistance
- nitric oxide
- anti inflammatory
- stem cells
- health promotion
- pi k akt
- squamous cell carcinoma
- squamous cell
- toll like receptor
- metabolic syndrome
- adipose tissue
- lps induced
- cell proliferation
- coronary artery disease
- risk assessment
- genetic diversity
- cardiovascular events