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.
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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