Neuropeptide Y- and Vasoactive Intestinal Polypeptide-Containing Nerve Fibers in the Human Cerebral Arteries: Characteristics of Distribution

Angiology ◽  
1991 ◽  
Vol 42 (1) ◽  
pp. 35-43 ◽  
Author(s):  
Koji Kawamura ◽  
Noriyuki Sakata ◽  
Shigeo Takebayashi
1990 ◽  
Vol 113 (2) ◽  
pp. 121-126 ◽  
Author(s):  
Eric Maubert ◽  
Gérard Tramu ◽  
Dominique Croix ◽  
Jean Claude Beauvillain ◽  
Jean Paul Dupouy

2000 ◽  
Vol 20 (8) ◽  
pp. 1205-1214 ◽  
Author(s):  
Jan Fahrenkrug ◽  
Jens Hannibal ◽  
Jeppe Tams ◽  
Birgitte Georg

The two structurally related peptides, vasoactive intestinal polypeptide (VIP) and pituitary adenylate cyclase activating polypeptide (PACAP), are present in cerebral vascular nerve fibers. Biologic actions of VIP are exerted through two receptors, VPAC1 and VPAC2, having similar binding affinity for both VIP and PACAP. In the current study, the authors have developed a specific antibody against the rVPAC1 receptor to examine the localization of rVPAC1 immunoreactivity in cerebral arteries and arterioles of the rat by immunohistochemistry using fluorescence confocal microscopy. Specificity of the antiserum was ensured by immunoblotting and immunocytochemistry of cells transfected with cDNA encoding the different PACAP-VIP receptor subtypes. The rVPAC1 receptor immunoreactivity was localized to the plasmalemma of circularly orientated smooth muscle cells on superficial cerebral arteries and arterioles taken from the basal surface of the brain. By double immunostaining VIP immunoreactive nerve fibers and, to a lesser extent, those containing PACAP were shown to have intimate contact with the receptor protein. Vasoactive intestinal polypeptide and PACAP containing cerebrovascular nerve fibers were found in separate nerve populations with different distribution pattern and density. In brain sections processes of cortical VIP-, but not PACAP-, containing neurons seemed to innervate the rVPAC1 receptor of pial arterioles on the brain surface. The current findings provide the neuroanatomical substrate for a role of VIP and maybe PACAP in the regulation of cerebral blood flow.


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