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dynorphin a การใช้

ประโยคมือถือ
  • Forced swim stress increases the levels of dynorphin A in the hippocampus.
  • It also inhibits the degradation of met-enkephalin, dynorphin A, and other endogenous peptides.
  • Neurokinin b is expressed along with the peptides kisspeptin and dynorphin A in the neuronal cells of the arcuate nucleus.
  • It is a high conditioned place " aversion ", an effect which is dynorphin A-dependent.
  • Lai et al . studied the effects of dynorphin A 2-13 that did not contain the N-terminal tyrosine.
  • Likewise, classical opioid receptors possess little affinity towards NOP s endogenous ligand nociceptin, which is structurally related to dynorphin A.
  • Big dynorphin is more potent at KORs than is dynorphin A . Both big dynorphin and dynorphin A are more potent and more selective than dynorphin B.
  • Big dynorphin is more potent at KORs than is dynorphin A . Both big dynorphin and dynorphin A are more potent and more selective than dynorphin B.
  • The KOR is a type of opioid receptor that binds the opioid peptide dynorphin as the primary endogenous ligand ( substrate naturally occurring in the body ).
  • Based on the results of dynorphin A 2-13, the authors proposed a mechanism in which dynorphin A activates bradykinin receptors and thus stimulates pain response.
  • Based on the results of dynorphin A 2-13, the authors proposed a mechanism in which dynorphin A activates bradykinin receptors and thus stimulates pain response.
  • Big dynorphin and dynorphin A have the same selectivity for human KOR, but dynorphin A is more selective for KOR over MOR and DOR than is big dynorphin.
  • Big dynorphin and dynorphin A have the same selectivity for human KOR, but dynorphin A is more selective for KOR over MOR and DOR than is big dynorphin.
  • "' Zyklophin "'is a semisynthetic peptide derived from dynorphin A and a highly selective stress-induced reinstatement of cocaine-seeking in animals.
  • However, when dynorphin A 1-13 was injected into the intracerebroventriulcar ( ICV ) region of the brain, it had an antagonist effect on morphine-induced analgesia.
  • When prodynorphin is cleaved during processing by proprotein convertase 2 ( PC2 ), multiple active peptides are released : dynorphin A, dynorphin B, and vesicles in the presynaptic terminal.
  • Occasionally, prodynorphin is not fully processed, leading to the release of  big dynorphin .  This 32-amino acid molecule consists of both dynorphin A and dynorphin B.
  • The group found that while food did not alter the expression of dynorphin B, it increases dynorphin A levels in several rat brain regions ( hypothalamus, nucleus accumbens, and bed nucleus of the stria terminalis ).
  • The authors found that combining subanalgesic levels of morphine and dynorphin A 1-13, a version of dynorphin A containing only the first 13 amino acids of the peptide, in the rat spinal cord had additive effects.
  • The authors found that combining subanalgesic levels of morphine and dynorphin A 1-13, a version of dynorphin A containing only the first 13 amino acids of the peptide, in the rat spinal cord had additive effects.
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