Neuropeptide FF, a mammalian neuropeptide with multiple functions

被引:208
作者
Panula, P
Aarnisalo, AA
Wasowicz, K
机构
[1] ABO AKAD UNIV, DEPT BIOL, SF-20520 TURKU, FINLAND
[2] HELSINKI UNIV, DIV ANAT, DEPT BIOMED SCI, SF-00014 HELSINKI, FINLAND
关键词
D O I
10.1016/0301-0082(96)00001-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuropeptide FF (NPFF) and neuropeptide AF (NPAF) are two mammalian amidated neuropeptides which are highly concentrated in the posterior pituitary, spinal cord, hypothalamus and medulla. One precursor protein has been identified in mouse, rat, bovine and human brain. The precursor contains a single copy of both peptides, followed by a glycine residues necessary for amidation and flanked by basic residues necessary for processing by enzymes. In the brain, NPFF-like immunoreactive neurons are found in the hypothalamus and medulla. These systems may be associated with observed effects of NPFF on memory and autonomic regulation, respectively. A hypothalamo-pituitary pathway may be involved in neuroendocrine regulation. This is supported by lack of NPFF in the pituitary gland of vasopressin-deficient Brattleboro rats. It is also possible that NPFF acts as a hormone, as it has been detected in human plasma. The spinal cord contains an intrinsic NPFF-ir neuron system, with cell bodies in the dorsal horn and around the central canal. Nerve terminals are highly concentrated in the superficial laminae of the dorsal horn, where NPFF-immunoreactivity can be released by, e.g., potassium and substance P. One specific high-affinity binding site, distinct from binding sites for other peptides, has been characterized in the rat and human brain and spinal cord. The NPFF receptor appears to be coupled to a G-protein, but derails of the second messenger systems have not been clarified yet. Intracerebroventricular injection of NPFF induces a vigorous abstinence syndrome in morphine-tolerant rats. Although clear antiopioid-like efffects of NPFF on pain have been observed, some studies have also demonstrated long-lasting analgesic effects. These findings and the observed increase in NPFF-immunoreactivity in the cerebrospinal fluid during development of opiate tolerance render NPFF an interesting and challenging target of investigation. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:461 / +
相关论文
共 95 条
[21]  
GICQUEL S, 1994, J MED CHEM
[22]   ANTINOCICEPTIVE EFFECTS OF INTRATHECALLY ADMINISTERED F8FAMIDE AND FMRFAMIDE IN THE RAT [J].
GOUARDERES, C ;
SUTAK, M ;
ZAJAC, JM ;
JHAMANDAS, K .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1993, 237 (01) :73-81
[23]   ELECTROPHYSIOLOGICAL EFFECTS OF FLFQPQRF AMIDE, AN ENDOGENOUS BRAIN MORPHINE MODULATING PEPTIDE, ON CULTURED MOUSE SPINAL-CORD NEURONS [J].
GUZMAN, A ;
LEGENDRE, P ;
ALLARD, M ;
GEOFFRE, S ;
VINCENT, JD ;
SIMONNET, G .
NEUROPEPTIDES, 1989, 14 (04) :253-261
[24]  
HOLLT V, 1981, NEUROENDOCRINOLOGY, V22, P333
[25]   THE EFFECT OF PHE-MET-ARG-PHE-NH2 (FMRFAMIDE) ON MORPHINE-INDUCED INHIBITION OF COLONIC PROPULSIVE MOTILITY IN MICE [J].
JACOBY, MB ;
JACOBY, HI ;
MATHIASEN, JR ;
RAFFA, RB .
NEUROSCIENCE LETTERS, 1987, 83 (1-2) :128-132
[26]   THE ANALYSIS OF POST-TETANIC POTENTIATION IN GUINEA-PIG ILEUM LONGITUDINAL MUSCLE STRIP [J].
KADLEC, O ;
SEFERNA, I ;
MASEK, K ;
SOMOGYI, GT ;
KNOLL, J .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1982, 79 (3-4) :245-255
[27]   INHIBITORY INFLUENCES OF MAMMALIAN FMRFAMIDE (PHE-MET-ARG-PHE-AMIDE)-RELATED PEPTIDES ON NOCICEPTION AND MORPHINE-INDUCED AND STRESS-INDUCED ANALGESIA IN MICE [J].
KAVALIERS, M .
NEUROSCIENCE LETTERS, 1990, 115 (2-3) :307-312
[28]   IGG FROM ANTISERUM AGAINST ENDOGENOUS MAMMALIAN FMRF-NH2-RELATED PEPTIDES AUGMENTS MORPHINE-INDUCED AND STRESS-INDUCED ANALGESIA IN MICE [J].
KAVALIERS, M ;
YANG, HYT .
PEPTIDES, 1989, 10 (04) :741-745
[29]   SEX-DIFFERENCES IN THE EFFECTS OF NEUROPEPTIDE FF AND IGG FROM NEUROPEPTIDE FF ON MORPHINE-INDUCED AND STRESS-INDUCED ANALGESIA [J].
KAVALIERS, M ;
INNES, D .
PEPTIDES, 1992, 13 (03) :603-607
[30]   FMRFAMIDE - AN ENDOGENOUS PEPTIDE WITH MARKED INHIBITORY EFFECTS ON OPIOID-INDUCED FEEDING-BEHAVIOR [J].
KAVALIERS, M ;
HIRST, M .
BRAIN RESEARCH BULLETIN, 1986, 17 (03) :403-408