The effect of agmatine was related to activation of imidazoline receptor.
胍丁胺上述作用与激活咪唑啉受体有关。
参考来源 - 胍丁胺抗吗啡精神依赖及其作用机制So it is believed that agmatine may serve as a novel neurotransmitter and/or neuromodulator.
因而，普遍认为胍丁胺可能是脑内一种新的神经递质和/或调质。
参考来源 - 胍丁胺对大鼠海马和穹隆下器神经元放电的影响·2,447,543篇论文数据，部分数据来源于NoteExpress
胍丁胺是左旋精氨酸在左旋精氨酸脱羧酶催化下脱羧基的产物，是咪唑啉受体的内源性配体。
Agmatine formed by the decarboxylation of L-Arginine by the enzyme L-arginine decarboxylase, has been postulated to be an endogenous ligand for imidazoline receptors (I-R).
结论抑制慢性吗啡注射所引起的脊髓jnk的激活可能是胍丁胺抗吗啡镇痛耐受的作用机制之一。
Conclusion Inhibition of chronic morphine-induced spinal JNK activation may be one of the mechanisms underlying the blockage of morphine antinociceptive tolerance by agmatine.
本发明涉及一种沙丁胺醇修饰胍基化壳聚糖与制备方法和应用。
The invention relates to salbutamol modified guanidinated chitosan and a preparation method and application thereof.
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