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Beta-casomorphin-5 stimulates neurite outgrowth in a mouse neuroblastoma cell line (Neuro-2a).

机译:Beta-casomorphin-5刺激小鼠神经母细胞瘤细胞系(Neuro-2a)中的神经突生长。

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摘要

We studied the effect of beta-casomorphin-5 (mu-acting opioid peptides derived from milk protein beta-casein) on neurite outgrowth of mouse neuroblastoma cell line, Neuro-2a. Beta-casomorphin-5 stimulated neurite outgrowth of Neuro-2a cells in a naloxone-reversible manner. The stimulating effect of beta-casomorphin-5 was observed even at picomolar concentrations. The selective mu-agonist, (D-Ala2, N-Me-Phe4, Gly5-ol)-enkephalin (DAMGO) exhibited the similar stimulating effect only at micromolar concentrations. On the other hand, (D-Pen(2,5))-enkephalin (DPDPE) (a delta-agonist), U-50,488 (a kappa-agonist), and endogenous opioid peptides, such as enkephalins and dynorphin A (1-13), showed no such stimulating effect. These results suggest that the neurite outgrowth-stimulating action of beta-casomorphin-5 may be mediated via a receptor which has mu-like characteristics and high sensitivity to beta-casomorphin-5, and that beta-casomorphins may play a role as a neurite elongation factor during the suckling period.
机译:我们研究了β-casomorphin-5(源自牛奶蛋白β-酪蛋白的μ-作用阿片肽)对小鼠神经母细胞瘤细胞系Neuro-2a神经突生长的影响。 Beta-casomorphin-5以纳洛酮可逆的方式刺激Neuro-2a细胞的神经突生长。即使在皮摩尔浓度下也观察到了β-casomorphin-5的刺激作用。选择性的μ-激动剂,(D-Ala2,N-Me-Phe4,Gly5-ol)-脑啡肽(DAMGO)仅在微摩尔浓度下显示出相似的刺激作用。另一方面,(D-Pen(2,5))-脑啡肽(DPDPE)(δ激动剂),U-50488(κ激动剂)和内源性阿片肽,例如脑啡肽和强啡肽A(1 -13),没有显示出这种刺激作用。这些结果表明,β-casomorphin-5的神经突增生作用可能是通过具有mu-like特性和对β-casomorphin-5的高敏感性的受体介导的,并且β-casomorphin可能起神经突的作用。哺乳期的伸长率。

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