Central oxytocin enhances antinociception in the rat.

No abstract is available for this paper.

• Publication year

  2007

• Venue

  Peptides

• Publication date

  2007-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/J.PEPTIDES.2007.03.003PMID 17420069
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Arginine vasopressin in periaqueductal gray, which relates to antinociception, comes from hypothalamic paraventricular nucleus in the rat.

  2007cited by this paper
• Periaqueductal gray knockdown of V2, not V1a and V1b receptor influences nociception in the rat. yj6676@yahoo.com.

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• RETRACTED: Periaqueductal gray knockdown of V2, not V1a and V1b receptor influences nociception in the rat

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• Arginine vasopressin enhances periaqueductal gray synthesis and secretion of enkephalin and endorphin in the rat.

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• Through V2, not V1 receptor relating to endogenous opiate peptides, arginine vasopressin in periaqueductal gray regulates antinociception in the rat.

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• Through central arginine vasopressin, not oxytocin and endogenous opiate peptides, glutamate sodium induces hypothalamic paraventricular nucleus enhancing acupuncture analgesia in the rat.

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• Only through the brain nuclei, arginine vasopressin regulates antinociception in the rat.

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• Arginine vasopressin in the caudate nucleus plays an antinociceptive role in the rat.

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• Effect of arginine vasopressin in the nucleus raphe magnus on antinociception in the rat.

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• Only arginine vasopressin, not oxytocin and endogenous opiate peptides, in hypothalamic paraventricular nucleus play a role in acupuncture analgesia in the rat.

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• Through the central V2, not V1 receptors influencing the endogenous opiate peptide system, arginine vasopressin, not oxytocin in the hypothalamic paraventricular nucleus involves in the antinociception in the rat.

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