4.7 Article

Osthole inhibits histamine-dependent itch via modulating TRPV1 activity

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SCIENTIFIC REPORTS
卷 6, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep25657

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资金

  1. Natural Science Foundation of China (NSFC) [31271181, 31471007, 31400950]
  2. Overseas and Hong Kong, Macau Scholars Collaborative Research Fund [31328012]
  3. Natural Science Foundation of Jiangsu Province [BK20130953]
  4. traditional Chinese Medicine of Jiangsu Province [Lz13020]
  5. Natural Science Foundation of Guangxi Province [2015GXNSFBA139138]
  6. Science and Technology Development Program of Hunan Province [2013FJ2012]
  7. Guangxi University of Chinese Medicine [QN14001]
  8. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  9. Qing Lan Project in Jiangsu Province
  10. Jiangsu Collaborative Innovation Center of Traditional Chinese Medicine (TCM) Prevention and Treatment of Tumor
  11. Hunan cooperative Innovation Center for Molecular Target New Drug Study

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Osthole, an active coumarin isolated from Cnidium monnieri (L.) Cusson, has long been used in China as an antipruritic herbal medicine; however, the antipruitic mechanism of osthole is unknown. We studied the molecular mechanism of osthole in histamine-dependent itch by behavioral test, Ca2+ imaging, and electrophysiological experiments. First, osthole clearly remitted the scratching behaviors of mice induced with histamine, HTMT, and VUF8430. Second, in cultured dorsal root ganglion (DRG) neurons, osthole showed a dose-dependent inhibitory effect to histamine. On the same neurons, osthole also decreased the response to capsaicin and histamine. In further tests, the capsaicin-induced inward currents were inhibited by osthole. These results revealed that osthole inhibited histamine-dependent itch by modulating TRPV1 activity. This study will be helpful in understanding how osthole exerts anti-pruritus effects and suggests that osthole may be a useful treatment medicine for histamine-dependent itch.

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