Rescue of cognitive-aging by administration of a neurogenic and/or neurotrophic compound.
Bolognin. Silvia S; Buffelli. Mario M; Puoliväli. Jukka J; Iqbal. Khalid K
Key Findings
- Oral P021 reduced age‑related decline in learning and memory in 22‑24‑month‑old rats.
- P021 restored neurogenesis and increased brain‑derived neurotrophic factor (BDNF) levels.
- Synaptic deficits in the cortex and hippocampus were repaired, and myoinositol levels in the hippocampus dropped.
Practical Outcomes
- P021 shows that a orally delivered neurotrophic peptide can counteract cognitive aging in animal models, suggesting a potential supplement route for humans. However, the study is limited to rats, with no human dosing or safety data, so biohackers should view it as promising but experimental and await further research before trying it.
Summary
Giving rats a small peptide called P021 by mouth for a long time helped older rats keep their memory and learning abilities. The peptide boosted brain growth factors, improved the creation of new brain cells, fixed synapse problems, and lowered a brain chemical (myoinositol) that usually goes up with age.
Abstract
Aging is characterized by a progressive decline of cognitive performance, which has been partially attributed to structural and functional alterations of hippocampus. Importantly, aging is the major risk factor for the development of neurodegenerative diseases, especially Alzheimer's disease. An important therapeutic approach to counteract the age-associated memory dysfunctions is to maintain an appropriate microenvironment for successful neurogenesis and synaptic plasticity. In this study, we show that chronic oral administration of peptide 021 (P021), a small peptidergic neurotrophic compound derived from the ciliary neurotrophic factor, significantly reduced the age-dependent decline in learning and memory in 22 to 24-month-old Fisher rats. Treatment with P021 inhibited the deficit in neurogenesis in the aged rats and increased the expression of brain derived neurotrophic factor. Furthermore, P021 restored synaptic deficits both in the cortex and the hippocampus. In vivo magnetic resonance spectroscopy revealed age-dependent alterations in hippocampal content of several metabolites. Remarkably, P021 was effective in significantly reducing myoinositol (INS) concentration, which was increased in aged compared with young rats. These findings suggest that stimulating endogenous neuroprotective mechanisms is a potential therapeutic approach to cognitive aging, Alzheimer's disease, and associated neurodegenerative disorders and P021 is a promising compound for this purpose.
Study Information
pubmed
2014
2014-03-02T00:00:00.000Z
10.1016/j.neurobiolaging.2014.02.017
50
95