VASCULAR PROTEIN LEAKAGE IN THE RAT PAROTID-GLAND ELICITED BY REFLEX STIMULATION, PARASYMPATHETIC NERVE-STIMULATION AND ADMINISTRATION OF NEUROPEPTIDES
A. Asztely et al., VASCULAR PROTEIN LEAKAGE IN THE RAT PAROTID-GLAND ELICITED BY REFLEX STIMULATION, PARASYMPATHETIC NERVE-STIMULATION AND ADMINISTRATION OF NEUROPEPTIDES, Regulatory peptides, 77(1-3), 1998, pp. 113-120
Evans blue accumulated in parotid glands of conscious rats in response
to feeding (over 60 min), in the absence of atropine and adrenoceptor
antagonists and in their presence, and after pretreatment with the se
nsory neurotoxin capsaicin. Stimulation of the auriculo-temporal nerve
(40 Hz, 10 or 20 min), without and with the blockers, caused Evans bl
ue to accumulate. A periglandular oedema also contained the dye. Admin
istration (i.v.) of neurokinin A accumulated Evans blue, while substan
ce P, vasoactive intestinal peptide (VIP), pituitary adenylate cyclase
-activating peptide (PACAP), calcitonin gene-related peptide (CGRP) an
d pilocarpine lacked effect. Pilocarpine enhanced the action of neurok
inin A and, furthermore, substance P combined with either VIP, PACAP o
r CGRP resulted in accumulation of Evans blue. In the sublingual + sub
mandibular glands, Evans blue increased in response to neurokinin A an
d pilocarpine; furthermore, substance P and VIP, and substance P and C
GRP, interacted positively. Bradykinin lacked effect in the glands. Co
mparisons were made with the urinary bladder. Accumulation of Evans bl
ue reflects plasma protein extravasation. In salivary glands, the phen
omenon occurred during feeding and was independent on intact sensory i
nnervation; instead, the parasympathetic innervation containing the ne
uropeptides was in focus. In the clinic, the present findings may have
implications for the aetiology of gland swelling and pain. (C) 1998 E
lsevier Science B.V. All rights reserved.