{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T15:59:28Z","timestamp":1791561568892,"version":"4.3.4"},"reference-count":42,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T00:00:00Z","timestamp":1767139200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T00:00:00Z","timestamp":1767139200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Brain and Behavior"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>This study systematically investigated the effects and molecular mechanisms of Baishaoluoshi Decoction (BD) on synaptic plasticity in rats with post\u2010stroke spasticity (PSS).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>A rat model of PSS was established using middle cerebral artery occlusion. Behavioral assessments, including modified neurological severity scores, rotarod tests, and the Modified Ashworth Scale, were employed. Synaptic ultrastructure was analyzed using transmission electron microscopy (TEM). The molecular mechanisms were explored using immunofluorescence and western blot analyses to evaluate protein expression (Nogo\u2010A, Nogo receptor (NgR), RhoA, Collapsin Response Mediator Protein 2 (CRMP2), and AGG) and NgR\/Olig2 colocalization. BD was also tested in combination with the NgR antagonist NEP1\u201040.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>BD significantly ameliorated the neurological deficits, prolonged rotarod fall latency, and reduced spasticity. TEM revealed that BD restored the synaptic ultrastructure in the peri\u2010infarct regions by increasing postsynaptic density (PSD) thickness and length, and narrowing synaptic clefts. BD downregulates synaptic\u2010plasticity\u2010related proteins (Nogo\u2010A, NgR, RhoA, AGG, and CRMP2) and attenuates oligodendrocyte\u2010mediated inhibitory signaling via reduced NgR\/Olig2 co\u2010localization. BD combined with NEP1\u201040 exhibits synergistic therapeutic efficacy.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>BD alleviates PSS by enhancing synaptic plasticity and suppressing inhibitory signaling through multitarget modulation of neuron\u2013glia interactions. These findings highlight BD as a promising therapeutic intervention for PSS, which is supported by molecular evidence of its effects on synaptic remodeling and functional recovery.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/brb3.71170","type":"journal-article","created":{"date-parts":[[2025,12,31]],"date-time":"2025-12-31T13:32:25Z","timestamp":1767187945000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Baishaoluoshi Decoction Mitigates Post\u2010Stroke Spasticity by Targeting Synaptic Plasticity Through the Nogo\u2010A\/NgR Signaling Pathway"],"prefix":"10.1002","volume":"16","author":[{"given":"Xiongxing","family":"Sun","sequence":"first","affiliation":[{"name":"Graduate School of Hunan University of Chinese Medicine  Changsha Hunan Province China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shanshan","family":"Zeng","sequence":"additional","affiliation":[{"name":"Hunan 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