4-Aminopyridine Induces Nerve Growth Factor to Improve Skin Wound Healing and Tissue Regeneration.
Mashanipalya G JagadeeshaprasadPrem Kumar GovindappaAmanda M NelsonMark D NobleJohn C ElfarPublished in: Biomedicines (2022)
The discovery of ways to enhance skin wound healing is of great importance due to the frequency of skin lesions. We discovered that 4-aminopyridine (4-AP), a potassium channel blocker approved by the FDA for improving walking ability in multiple sclerosis, greatly enhances skin wound healing. Benefits included faster wound closure, restoration of normal-appearing skin architecture, and reinnervation. Hair follicle neogenesis within the healed wounds was increased, both histologically and by analysis of K15 and K17 expression. 4-AP increased levels of vimentin (fibroblasts) and alpha-smooth muscle actin (α-SMA, collagen-producing myofibroblasts) in the healed dermis. 4-AP also increased neuronal regeneration with increased numbers of axons and S100 + Schwann cells (SCs), and increased expression of SRY-Box Transcription Factor 10 (SOX10). Treatment also increased levels of transforming growth factor-β (TGF-β), substance P, and nerve growth factor (NGF), important promoters of wound healing. In vitro studies demonstrated that 4-AP induced nerve growth factor and enhanced proliferation and migration of human keratinocytes. Thus, 4-AP enhanced many of the key attributes of successful wound healing and offers a promising new approach to enhance skin wound healing and tissue regeneration.
Keyphrases
- wound healing
- growth factor
- transcription factor
- transforming growth factor
- multiple sclerosis
- smooth muscle
- poor prognosis
- stem cells
- epithelial mesenchymal transition
- peripheral nerve
- dna binding
- induced apoptosis
- small molecule
- binding protein
- oxidative stress
- genome wide identification
- brain injury
- drug induced
- high glucose
- cell cycle arrest
- induced pluripotent stem cells
- angiotensin converting enzyme
- cerebral ischemia
- long non coding rna