Pierce T L, Grahek M D, Wessendorf M W
Department of Cell Biology and Neuroanatomy, University of Minnesota, Minneapolis 55455, USA.
Neuroreport. 1998 Feb 16;9(3):385-9. doi: 10.1097/00001756-199802160-00005.
Antisera were raised against endomorphin-2, a recently isolated endogenous opioid peptide that binds potently and selectively to the mu-opioid receptor. When sections of spinal cord were stained immunocytochemically, a dense plexus of fibres and varicosities was visualized in the superficial dorsal horn of rats and one monkey. Following unilateral multiple dorsal rhizotomy, labeling for endomorphin-2 was markedly reduced ipsilateral to the lesion. In sections stained for both endomorphin-2 and CGRP, double-labeling was observed. Taken together, these data suggest that endomorphin-2 occurs in small diameter primary afferent fibres in rodents and primates. It appears possible that the release of neurotransmitters from nociceptive primary afferents might be regulated by release of endomorphin-2 from primary afferent terminals.
制备了针对内吗啡肽-2的抗血清,内吗啡肽-2是一种最近分离出的内源性阿片肽,它能有效且选择性地与μ-阿片受体结合。当对脊髓切片进行免疫细胞化学染色时,在大鼠和一只猴子的脊髓背角浅层可见密集的纤维和曲张体丛。单侧多处背根切断术后,损伤同侧内吗啡肽-2的标记明显减少。在对内吗啡肽-2和降钙素基因相关肽(CGRP)进行染色的切片中,观察到了双标记。综合这些数据表明,内吗啡肽-2存在于啮齿动物和灵长类动物的小直径初级传入纤维中。伤害性初级传入神经释放神经递质可能受初级传入神经末梢释放内吗啡肽-2的调节,这似乎是有可能的。