# 5-HT1B receptor agonists promote Schwann cell myelination

**Authors:** Yuka Kobayashi-Ujiie, Keiko Hiraki-Kamon, Shuji Wakatsuki, Toshiyuki Araki

PMC · DOI: 10.1371/journal.pone.0345946 · PLOS One · 2026-03-27

## TL;DR

This paper shows that a drug called zolmitriptan can help Schwann cells form myelin, which may help treat a type of nerve disease that affects movement.

## Contribution

The study identifies 5-HT1B/1D receptor agonists as potential therapeutics for peripheral hypomyelinating neuropathy.

## Key findings

- Zolmitriptan promotes myelination in cultured dorsal root ganglia explants from Tr-Ncnp mice.
- Chronic administration of zolmitriptan improves sensorimotor function in Tr-Ncnp mice.
- Zolmitriptan up-regulates myelin-related genes and increases Schwann cell proliferation.

## Abstract

Congenital demyelinating peripheral neuropathy causes severe sensorimotor defects, affecting patient mobility. To identify therapeutic compounds for peripheral hypomyelinating neuropathy, we performed an unbiased screening of annotated compound library by in vitro myelination culture model using Trembler (Tr-Ncnp) -derived dorsal root ganglia explants. Among the compounds identified in the screening, we confirmed that zolmitriptan, a 5-hydroxytryptamine 1B/1D receptor agonist, promotes myelination in culture. Zolmitriptan up-regulated myelin-related genes in primary Schwann cells and increased proliferating Schwann cells along axons in DRG explant cultures of Tr-Ncnp mice. Furthermore, we observed that chronic administration of zolmitriptan ameliorates sensorimotor dysfunction in Tr-Ncnp mice. Collectively, these results suggest that 5-HT1B/1D receptor agonists may increase Schwann cells participating in myelination, and consequently ameliorate myelination impairment in peripheral neuropathy.

## Linked entities

- **Chemicals:** zolmitriptan (PubChem CID 60857)

## Full-text entities

- **Genes:** Egf (epidermal growth factor) [NCBI Gene 25313], Egr2 (early growth response 2) [NCBI Gene 13654] {aka Egr-2, Krox-20, Krox20, NGF1-B, Zfp-25, Zfp-6}, Pou3f1 (POU domain, class 3, transcription factor 1) [NCBI Gene 18991] {aka Oct-6, Oct6, Otf-6, Otf6, Scip, Test1}, Nefm (neurofilament, medium polypeptide) [NCBI Gene 18040] {aka NF-M, NF160, NF165, Nef3, Nfm}, Ngfr (nerve growth factor receptor (TNFR superfamily, member 16)) [NCBI Gene 18053] {aka LNGFR, Tnfrsf16, p75, p75NGFR, p75NTR}, Actb (actin, beta) [NCBI Gene 81822] {aka Actx}, Ngf (nerve growth factor) [NCBI Gene 18049] {aka Ngfb, beta-NGF}, Pmp22 (peripheral myelin protein 22) [NCBI Gene 18858] {aka Gas-3, HNPP, PMP-22, TRE002, Tr, trembler}, Mpz (myelin protein zero) [NCBI Gene 17528] {aka Mpp, P-zero, P0}, Htr1b (5-hydroxytryptamine (serotonin) receptor 1B) [NCBI Gene 15551] {aka 5-HT-1B}, Mbp (myelin basic protein) [NCBI Gene 24547] {aka Mbps}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Htr2a (5-hydroxytryptamine (serotonin) receptor 2A) [NCBI Gene 15558] {aka 5-HT-2, 5-HT-2A, E030013E04, Htr-2, Htr2}, Mbp (myelin basic protein) [NCBI Gene 17196] {aka Hmbpr, golli-mbp, jve, mld, shi}
- **Diseases:** sensorimotor (MESH:D020233), dislocation (MESH:D004204), cerebellar atrophy (MESH:D002526), tremor (MESH:D014202), CMT1E (MESH:C537986), hereditary neurologic disorder (MESH:D009386), defective myelination (MESH:D003711), death (MESH:D003643), impairment of peripheral nerve function (MESH:D010523), hereditary motor and sensory neuropathies (MESH:D015417), HNPP (MESH:C536965), CMT (MESH:D002607), instability (MESH:D043171), myelin impairment (MESH:D020279), peripheral nerve demyelination (MESH:D011129), muscle relaxant (MESH:D019042)
- **Chemicals:** PBS (MESH:D007854), DMSO (MESH:D004121), Penicillin (MESH:D010406), Sumatriptan (MESH:D018170), butorphanol (MESH:D002077), saline (MESH:D012965), N2 (MESH:D009584), cytosine arabinoside (MESH:D003561), Zol (MESH:D000077211), water (MESH:D014867), osmium (VIII) oxide (MESH:D009993), L-ascorbic acid (MESH:D001205), forskolin (MESH:D005576), SB224289 (MESH:C108518), glutaraldehyde (MESH:D005976), EdU (MESH:C022811), SYBR green (MESH:C098022), Epon 812 (MESH:C004875), Alexa fluorophores (-), Streptomycin (MESH:D013307), calcium (MESH:D002118), Zolmitriptan (MESH:C089750), Phenytoin sodium (MESH:D010672), lipid (MESH:D008055), uranyl acetate (MESH:C005460), EDTA (MESH:D004492), Glycerol (MESH:D005990), medetomidine (MESH:D020926), telotristat (MESH:C000592493), F12 (MESH:C007782), candesartan (MESH:C081643), Glutamax (MESH:C054122), midazolam (MESH:D008874), paraformaldehyde (MESH:C003043), DAPI (MESH:C007293), SDS (MESH:D012967)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** Leu16Pro, A leucine-to-proline
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), DRG — Danio rerio (Zebrafish), Spontaneously immortalized cell line (CVCL_IX16)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028473/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028473/full.md

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Source: https://tomesphere.com/paper/PMC13028473