TY - JOUR
T1 - Efficacy profile of noninvasive vagus nerve stimulation on cortical spreading depression susceptibility and the tissue response in a rat model
AU - Liu, Tzu-Ting
AU - Morais, Andreia
AU - Takizawa, Tsubasa
AU - Mulder, Inge
AU - Simon, Bruce J.
AU - Chen, Shih-Pin
AU - Wang, Shuu-Jiun
AU - Ayata, Cenk
AU - Yen, Jiin-Cherng
N1 - Funding Information: This work was funded by research grant from Ministry of Science and Technology of Taiwan [MOST-109-2314-B-010-040 (to JCY); MOST-107-2314-B-010-021, 108-2314-B-010-022-MY3 & 110-2326-B-A49A-501-MY3 (to SPC); MOST 108-2321-B-010-014-MY2, 108-2321-B-010-001-, 108-2314-B-010-023-MY3, 110-2321-B-010-005- & 111-2321-B-010-004 (to SJW)], Taipei Veterans General Hospital, Taiwan [VGH-106-D9-001-MY2-2 (to SJW) & V110C-102, V109D52-001-MY3-2, VGHUST110-G1-3-1 (to SPC)], and the Brain Research Center, National Yang-Ming University, from The Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education in Taiwan (to SPC); National Institute of Health [R01-2016D007667 (to CAyata)], the Massachusetts General Hospital [Claflin Distinguished Award, KEH]; This work is particularly supported by “Yin Yen-Liang Foundation Development and Construction Plan” of the College of Medicine, National Yang Ming Chiao Tung University. Publisher Copyright: © 2022, The Author(s).
PY - 2022/12/1
Y1 - 2022/12/1
N2 - Background: Noninvasive vagus nerve stimulation (nVNS) has recently emerged as a promising therapy for migraine. We previously demonstrated that vagus nerve stimulation inhibits cortical spreading depression (CSD), the electrophysiological event underlying migraine aura and triggering headache; however, the optimal nVNS paradigm has not been defined. Methods: Various intensities and doses of nVNS were tested to improve efficacy on KCl-evoked CSD frequency and electrical threshold of CSD in a validated rat model. Chronic efficacy was evaluated by daily nVNS delivery for four weeks. We also examined the effects of nVNS on neuroinflammation and trigeminovascular activation by western blot and immunohistochemistry. Results: nVNS suppressed susceptibility to CSD in an intensity-dependent manner. Two 2-minute nVNS 5 min apart afforded the highest efficacy on electrical CSD threshold and frequency of KCl-evoked CSD. Daily nVNS for four weeks did not further enhance efficacy over a single nVNS 20 min prior to CSD. The optimal nVNS also attenuated CSD-induced upregulation of cortical cyclooxygenase-2, calcitonin gene-related peptide in trigeminal ganglia, and c-Fos expression in trigeminal nucleus caudalis. Conclusions: Our study provides insight on optimal nVNS parameters to suppress CSD and suggests its benefit on CSD-induced neuroinflammation and trigeminovascular activation in migraine treatment.
AB - Background: Noninvasive vagus nerve stimulation (nVNS) has recently emerged as a promising therapy for migraine. We previously demonstrated that vagus nerve stimulation inhibits cortical spreading depression (CSD), the electrophysiological event underlying migraine aura and triggering headache; however, the optimal nVNS paradigm has not been defined. Methods: Various intensities and doses of nVNS were tested to improve efficacy on KCl-evoked CSD frequency and electrical threshold of CSD in a validated rat model. Chronic efficacy was evaluated by daily nVNS delivery for four weeks. We also examined the effects of nVNS on neuroinflammation and trigeminovascular activation by western blot and immunohistochemistry. Results: nVNS suppressed susceptibility to CSD in an intensity-dependent manner. Two 2-minute nVNS 5 min apart afforded the highest efficacy on electrical CSD threshold and frequency of KCl-evoked CSD. Daily nVNS for four weeks did not further enhance efficacy over a single nVNS 20 min prior to CSD. The optimal nVNS also attenuated CSD-induced upregulation of cortical cyclooxygenase-2, calcitonin gene-related peptide in trigeminal ganglia, and c-Fos expression in trigeminal nucleus caudalis. Conclusions: Our study provides insight on optimal nVNS parameters to suppress CSD and suggests its benefit on CSD-induced neuroinflammation and trigeminovascular activation in migraine treatment.
KW - Cortical spreading depression
KW - Neuroinflammation
KW - Trigeminal activation
KW - Vagus nerve stimulation
UR - http://www.scopus.com/inward/record.url?scp=85123444570&partnerID=8YFLogxK
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85123444570&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/35062860
U2 - https://doi.org/10.1186/s10194-022-01384-1
DO - https://doi.org/10.1186/s10194-022-01384-1
M3 - Article
C2 - 35062860
SN - 1129-2369
VL - 23
SP - 12
JO - Journal of Headache and Pain
JF - Journal of Headache and Pain
IS - 1
M1 - 12
ER -