<?xml version='1.0' encoding='utf-8'?>
<?xml-stylesheet type="text/xsl" href="/v2/static/oai2.xsl"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-10-14T01:46:46Z</responseDate>
  <request identifier="oai:figshare.com:article/34009200" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/34009200</identifier>
        <datestamp>2026-09-28T05:36:11Z</datestamp>
        <setSpec>category_15</setSpec>
        <setSpec>portal_316</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_09_2026</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Data Sheet 1_Evaluation of peripheral and intranigral AAV-mediated Irisin delivery in a chronic AAV-A53T α-Synuclein overexpression mouse model of Parkinson’s disease.docx</dc:title>
          <dc:creator>Chunyan Shu (20999738)</dc:creator>
          <dc:creator>Jiehong Huang (23961144)</dc:creator>
          <dc:creator>Wandi Pu (25119807)</dc:creator>
          <dc:creator>Haoyuan Liang (25119810)</dc:creator>
          <dc:creator>Zucai Xu (9227159)</dc:creator>
          <dc:creator>Xijin Wang (5337419)</dc:creator>
          <dc:creator>Lixi Li (3170661)</dc:creator>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>AAV9-A53T</dc:subject>
          <dc:subject>Irisin</dc:subject>
          <dc:subject>neuroprotection</dc:subject>
          <dc:subject>Parkinson’s disease</dc:subject>
          <dc:subject>α-Synuclein</dc:subject>
          <dc:description>Background&lt;p&gt;Parkinson’s disease (PD) is characterized by progressive loss of dopaminergic neurons in the substantia nigra and pathological aggregation of α-Synuclein (α-Syn). Although Irisin has shown neuroprotective effects in acute MPTP-induced and α-Syn preformed fibrils (PFFs) propagation models, its therapeutic effects in a chronic α-Syn overexpression model remain incompletely defined.&lt;/p&gt;Methods&lt;p&gt;In the present study, we evaluated the effects of AAV8-Irisin delivered either peripherally via tail vein injection or centrally via direct intranigral co-administration in the AAV9-A53T mouse model.&lt;/p&gt;Results&lt;p&gt;Under the tested doses, routes, and intervention schedule, neither peripheral nor intranigral AAV8-Irisin delivery produced statistically significant improvements in behavioral performance, dopaminergic neuron survival, α-Synuclein pathology, glial activation, or AQP4 polarization; however, numerical trends were observed in select measures, including motor coordination and TH-positive neuron counts.&lt;/p&gt;Conclusion&lt;p&gt;These findings suggest that, under the current experimental conditions, a clear neuroprotective benefit of Irisin was not readily detectable in this model. Whether modest effects might emerge under different exposure levels, intervention windows, or adequately powered designs remains unknown.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T05:36:11Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fnagi.2026.1918326.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Data_Sheet_1_Evaluation_of_peripheral_and_intranigral_AAV-mediated_Irisin_delivery_in_a_chronic_AAV-A53T_-Synuclein_overexpression_mouse_model_of_Parkinson_s_disease_docx/34009200</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
