<?xml version='1.0' encoding='UTF-8'?>
<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>2026-03-10T18:44:10Z</responseDate>
  <request verb="GetRecord" metadataPrefix="oai_dc" identifier="oai:kumadai.repo.nii.ac.jp:00022407">https://kumadai.repo.nii.ac.jp/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:kumadai.repo.nii.ac.jp:00022407</identifier>
        <datestamp>2023-08-24T02:45:38Z</datestamp>
        <setSpec>413:443</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns="http://www.w3.org/2001/XMLSchema" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Nerve growth factor, interoception, and sympathetic neuron: Lesson from congenital insensitivity to pain with anhidrosis</dc:title>
          <dc:creator>Indo, Yasuhiro</dc:creator>
          <dc:creator>97413</dc:creator>
          <dc:creator>Indo, Yasuhiro</dc:creator>
          <dc:creator>93163</dc:creator>
          <dc:creator>犬童, 康弘</dc:creator>
          <dc:creator>インドウ, ヤスヒロ</dc:creator>
          <dc:subject>493</dc:subject>
          <dc:subject>Nerve growth factor (NGF)</dc:subject>
          <dc:subject>神経成長因子</dc:subject>
          <dc:subject>Receptor tyrosine kinase for NGF</dc:subject>
          <dc:subject>チロシンキナーゼ型神経成長因子受容体</dc:subject>
          <dc:subject>TrkA protein</dc:subject>
          <dc:subject>TrkA タンパク質</dc:subject>
          <dc:subject>NTRK1 gene</dc:subject>
          <dc:subject>NTRK1 遺伝子</dc:subject>
          <dc:subject>TRKA gene</dc:subject>
          <dc:subject>TRKA 遺伝子</dc:subject>
          <dc:subject>Congenital insensitivity to pain with anhidrosis</dc:subject>
          <dc:subject>先天性無痛無汗症</dc:subject>
          <dc:subject>Interoception</dc:subject>
          <dc:subject>内感覚</dc:subject>
          <dc:subject>Polymodal receptor</dc:subject>
          <dc:subject>ポリモーダル受容器</dc:subject>
          <dc:subject>Sympathetic neuron</dc:subject>
          <dc:subject>交感神経ニューロン</dc:subject>
          <dc:subject>Basal forebrain cholinergic neuron</dc:subject>
          <dc:subject>前脳基底野コリン作動性ニューロン</dc:subject>
          <dc:subject>Emotion</dc:subject>
          <dc:subject>情動</dc:subject>
          <dc:subject>Pain</dc:subject>
          <dc:subject>痛み</dc:subject>
          <dc:subject>疼痛</dc:subject>
          <dc:subject>Homeostasis</dc:subject>
          <dc:subject>恒常性</dc:subject>
          <dc:subject>Hereditary sensory and autonomic neuropathy type IV</dc:subject>
          <dc:subject>遺伝性感覚自律神経性ニュー ロパシー IV 型</dc:subject>
          <dc:description>application/pdf</dc:description>
          <dc:description>論文(Article)</dc:description>
          <dc:description>Nerve growth factor (NGF) is a well-known neurotrophic factor essential for the survival and maintenance of sensory and sympathetic neurons. Congenital insensitivity to pain with anhidrosis (CIPA) is a genetic disorder due to loss-of-function mutations in the NTRK1 (also known as TRKA) gene encoding TrkA, a receptor tyrosine kinase for NGF. Patients with CIPA provide us a rare opportunity to explore the developmental and physiological function of the NGF-dependent neurons in behavior, cognitive, and mental activities that are not available in animal studies. Here, I discuss the significance of findings that patients with CIPA lack NGF-dependent neurons, including interoceptive polymodal receptors, sympathetic postganglionic neurons, and probably several types of neurons in the brain. They also exhibit characteristic emotional behavior or problems. Together, the NGF-TrkA system is essential for the establishment of a neural network for interoception and homeostasis that may underlie 'gut feelings'. Thus, NGF-dependent neurons play a crucial role in emotional experiences and decision-making processes. Prospective studies focused on these neurons might provide further insights into the neural basis of human emotion and feeling.</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>Elsevier B.V.</dc:publisher>
          <dc:date>2009-05</dc:date>
          <dc:type>AM</dc:type>
          <dc:format>application/pdf</dc:format>
          <dc:identifier>Autonomic neuroscience: basic &amp; clinical</dc:identifier>
          <dc:identifier>1-2</dc:identifier>
          <dc:identifier>147</dc:identifier>
          <dc:identifier>3</dc:identifier>
          <dc:identifier>8</dc:identifier>
          <dc:identifier>AA11470577</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/record/22407/files/AN-09YI.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/2298/11429</dc:identifier>
          <dc:identifier>https://kumadai.repo.nii.ac.jp/records/22407</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>15660702</dc:relation>
          <dc:rights>Elsevier B.V.</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
