Dihexa
N-(1-Oxohexyl)-L-tyrosyl-N-(6-amino-6-oxohexyl)-L-isoleucinamide, N-hexanoic-Tyr-Ile-(6) aminohexanoic amide, PNB-0408
Stem cell, Granulocyte-Colony Stimulating Factor and/or Dihexa to promote limb function recovery in a rat sciatic nerve damage-repair model: Experimental animal studies.
Weiss. Jessica B JB; Phillips. Cody J CJ; Malin. Edward W EW; Gorantla. Vijay S VS; Harding. Joseph W JW; Salgar. Shashikumar K SK
Key Findings
- Sensory function in the injured leg returned to near‑normal levels by 8 weeks in all rats.
- Motor function (walking ability) was significantly better at 8‑16 weeks when mesenchymal stem cells were combined with Dihexa or G‑CSF, compared to control groups.
- Dihexa was administered at 2‑4 mg per kg body weight in rats and was delivered locally via hydrogel or systemically.
Practical Outcomes
- The study suggests Dihexa might boost nerve‑repair outcomes when used with stem cells, but the work is still in rats and the doses are not directly transferable to humans. For biohackers, it’s an interesting hint that Dihexa could have regenerative potential, yet more safety and human‑trial data are needed before any real‑world protocol can be designed.
Summary
In rats with a cut sciatic nerve, giving a mix of stem cells, a growth factor (G‑CSF), or the peptide Dihexa helped the leg muscles work better after surgery. All the rats got their feeling back in about 8 weeks, but the groups that got stem cells plus Dihexa (or G‑CSF) showed noticeably better walking ability than the others.
Abstract
Optimizing nerve regeneration and re-innervation of target muscle/s is the key for improved functional recovery following peripheral nerve damage. We investigated whether administration of mesenchymal stem cell (MSC), Granulocyte-Colony Stimulating Factor (G-CSF) and/or Dihexa can improve recovery of limb function following peripheral nerve damage in rat sciatic nerve transection-repair model. There were 10 experimental groups (n = 6-8 rats/group). Bone marrow derived syngeneic MSCs (2 × 10<sup>6</sup>; passage≤6), G-CSF (200-400 μg/kg b.wt.), Dihexa (2-4 mg/kg b.wt.) and/or Vehicle were administered to male Lewis rats locally via hydrogel at the site of nerve repair, systemically (i.v./i.p), and/or to gastrocnemius muscle. The limb sensory and motor functions were assessed at 1-2 week intervals post nerve repair until the study endpoint (16 weeks). The sensory function in all nerve boundaries (peroneal, tibial, sural) returned to nearly normal by 8 weeks (Grade 2.7 on a scale of Grade 0-3 [0 = No function; 3 = Normal function]) in all groups combined. The peroneal nerve function recovered quickly with return of function at one week (∼2.0) while sural nerve function recovered rather slowly at four weeks (∼1.0). Motor function at 8-16 weeks post-nerve repair as determined by walking foot print grades significantly (P < 0.05) improved with MSC + G-CSF or MSC + Dihexa administrations into gastrocnemius muscle and mitigated foot flexion contractures. These findings demonstrate MSC, G-CSF and Dihexa are promising candidates for adjunct therapies to promote limb functional recovery after surgical nerve repair, and have implications in peripheral nerve injury and limb transplantation. IACUC No.215064.
Study Information
pubmed
2021
2021-10-08T00:00:00.000Z
10.1016/j.amsu.2021.102917
2
88