Thermolytic salivation, substance P and kinins in rats

References

• Asztely A., Tobin G., Ekstrom J. Parasympathetic non-adrenergic, non-cholinergic reflex secretion of parotid acinar granules in rats pretreated with atropine and adrenoceptor antagonists. Regulat. Pept (1994); 51: 255–262
   PubMed Web of Science ®Google Scholar
• Berg T., Johansen L., Poulsen K. Exocrine and endocrine release of kallikrein after reflex-induced salivary secretion. Acta Physiol. Scand (1990); 139: 29–37
   PubMedGoogle Scholar
• Brodin E., Ekman R., Ekstrom J., Hakanson R., Sundler F. Effect of denervation on substance P and vasoactive intestinal peptide in rat salivary glands. J. Physiol (1983); 348: 67P
   Web of Science ®Google Scholar
• Buck S. H., Burcher E. The rat submaxillary gland contains predominantly P-type tachykinin binding sites. Peptides (1985); 6: 1079–1084
   PubMed Web of Science ®Google Scholar
• Chang M. M., Leeman S. E. Isolation of a sialogogic peptide from bovine hypothalamic tissue and its characterization as substance P. J. Biol. Chem (1970); 245: 4784–4790
   PubMed Web of Science ®Google Scholar
• Damas J. Water losses induced by heat exposure and the kinin system in the rat. Arch. int. Physiol. Bio-chim (1993); 101: 227–232
   Google Scholar
• Damas J. Kallikrein, nitric oxide and the vascular responses of the submaxillary glands in rats exposed to heat. Arch. Int. Physiol. Biochim (1994, a); 102: 139–146
   Google Scholar
• Damas J. Involvement of the kallikrein-kinin system in the salivary secretion elicited in rats by heat stress. Brazilian J. Med. Biol. Res (1994, b); 27: 2013–2020
   PubMed Web of Science ®Google Scholar
• Damas J., Adam A. Congenital deficiency in plasma kallikrein and kininogens in the Brown Norway rats. Experientia (1980); 36: 586–587
   PubMedGoogle Scholar
• Donnerer J., Amann R. The inhibition of neurogenic inflammation. Gen. Pharmac (1993); 24: 519–529
   PubMedGoogle Scholar
• Duner-Egström M., Larsson O., Fredholm B. B., Lunblad L., Fahrenkrug J., Lundberg J. M. Effects of acute and long-term atropine treatment on levels, release and response to Vip and Phi in the submandibular gland of cat and rat. Acta Physiol. Scand (1992); 146: 357–367
   PubMedGoogle Scholar
• Ekström J. Neuropeptides and secretion. J. Dent. Res (1987); 66: 524–530
   PubMed Web of Science ®Google Scholar
• Ekström J., Brodin E., Ekman R., Hakanson R., Sundler F. Vasoactive intestinal peptide and substance P in salivary gland of the rat following denervation and duct ligation. Regulat. Pept (1984); 10: 1–10
   PubMed Web of Science ®Google Scholar
• Gallagher D. V. Substance Pisa functional neurotransmitter in the rat parotid gland. J. Physiol. (London) (1983); 342: 483–498
   Google Scholar
• Garret C, Carruette A., Fardin V., Moussaoui S., Peyronel J. F., Blanchard J. C., Laduron P. Pharmacological properties of a potent and selective nonpeptide substance P antagonist. Proc. Natl. Acad. Sci. Usa (1991); 88: 10208–10212
   PubMed Web of Science ®Google Scholar
• Geppetti P. Sensory neuropeptide release by brady-kinin: mechanisms and pathophysiological implications. Regulat. Pept (1993); 47: 1–23
   PubMed Web of Science ®Google Scholar
• Goedert M., Nagy J. I., Emson P. C. The origin of substance P in the rat submandibular gland and its major duct. Brain Res (1982); 252: 327–333
   PubMed Web of Science ®Google Scholar
• Goll R., Poulsen Schmidt J. H., Schjoldager P. B., Poulsen S. S., Holst J. J. Peptide-evoked release of amylase from isolated acini of the rat parotid gland. Regulat. Pept (1994); 51: 237–254
   PubMed Web of Science ®Google Scholar
• Hainsworth F. R. Evaporative water loss from rats in the heat. Amer. J. Physiol (1968); 214: 979–982
   PubMed Web of Science ®Google Scholar
• Hainsworth F. R., Stricker E. M. Evaporative cooling in the rat: effects of partial desali vation. Amer. J. Physiol (1969); 217: 494–497
   PubMed Web of Science ®Google Scholar
• Hainsworth F. R., Stricker E. M. Evaporative cooling in the rat: further consideration of functional differences between salivary glands. Can. J. Physiol (1972); 50: 172–175
   PubMed Web of Science ®Google Scholar
• Jacques L., Couture R., Drapeau G., Regoli D. Capillary permeability induced by intravenous neurokinins. Naunyn-Schmiedeberg'sArch. Pharmacol (1989); 340: 170–179
   PubMed Web of Science ®Google Scholar
• Laniyonu A., Sliwinski-Lis E., Fleming N. Different tachykinin receptor subtypes are coupled to the phosphoinositide or cyclic Amp signal transduction pathways in rat submandibular cells. Febs Letters (1988); 240: 186–190
   PubMed Web of Science ®Google Scholar
• Legat F. J., Griesbacher T., Lembeck F. Mediation by bradykinin of rat paw oedema induced by collagenase from Clostridium histolyticum. Br. J. Pharmacol (1994); 112: 453–460
   PubMed Web of Science ®Google Scholar
• Lembeck F., Donnerer J., Bartho L. Inhibition of neurogenic vasodilatation and plasma extravasation by substance P antagonists, somatostatin and (D-Met2, Pro5)enkephalinamide. Eur. J. Pharmacol (1982); 85: 171–176
   PubMed Web of Science ®Google Scholar
• Lewis A. C., Rubini M. E., Beisel W. R. A method for rapid dehydration of rats. J. Appl. Physiol (1960); 15: 525–527
   PubMed Web of Science ®Google Scholar
• Lundberg J. M., Anggard A., Fahrenkrug J., Lundgren G., Holmstedt B. Corelease of Vip and acetylcholine in relation to blood flow and salivary secretion in cat submandibular salivary gland. Acta Physiol. Scand (1982); 115: 525–528
   Google Scholar
• Lundberg J. M., Saria A. Polypeptide containing neurons in airway smooth muscle. Ann. Rev. Physiol (1987); 49: 557–572
   PubMed Web of Science ®Google Scholar
• Maggio J. E. Tachykinins. Ann. Rev. Neuroscl (1988); 11: 13–28
   PubMed Web of Science ®Google Scholar
• Orstavik T. B. The distribution and secretion of kallikrein in some exocrine organs of the rat. Acta Physiol. Scand (1978); 104: 431–442
   PubMedGoogle Scholar
• Orstavik T. B., Carretero O. A., Johansen L., Scicli A. G. Role of kallikrein in the hypotensive effect of captopril after sympathetic stimulation of the rat submandibular gland. Circ. Res (1982); 51: 385–390
   PubMed Web of Science ®Google Scholar
• Rouissi N., Claing A., Nicolau M., Jukic D., ĎOrleans-Juste P., Regoli D. Substance P (Nk-1 receptor) antagonists: in vivo and in vitro activities in rats and guinea pigs. Life Sci (1993); 52: 1141–1147
   PubMed Web of Science ®Google Scholar
• Saria A., Lundberg J. M., Skofitsch G., Lembeck F. Vascular protein leakage in various tissues induced by substance P, capsaicin, bradykinin, serotonin, histamine and by antigen challenge. Naunyn Schmiede-berg's Arch. Pharmacol (1983); 324: 212–218
   PubMed Web of Science ®Google Scholar
• Sharkey K. A., Templeton D. Substance P in the rat parotid gland: evidence for a dual origin from the otic and trigeminal ganglia. Brain Res (1984); 304: 392–396
   PubMed Web of Science ®Google Scholar
• Takeda Y., Krause J. E. Neuropeptide K potently stimulates salivary gland secretion and potentiates substance-P-induced salivation. Proc. Natl. Acad. Sci. Usa (1989); 86: 392–396
   PubMed Web of Science ®Google Scholar
• Tobin G., Ekström J., Bloom S. R., Edwards A. V. Atropine-resistant submandibular responses to stimulation of the parasympathetic innervation in the anaesthetized ferret. J. Physiol (1991); 437: 327–339
   PubMed Web of Science ®Google Scholar
• Tobin G., Ekström J., Ekman R., Hakanson R. Influence of atropine on the depletion of vasoactive intestinal peptide, substance P and calcitonin gene-related peptide from rat parotid gland in response to parasympathetic stimulation. Acta Physiol. Scand (1994); 150: 463–465
   PubMedGoogle Scholar
• Virta E., Tornwall J., Uusitalo H. Substance P and neurokinin A immunoreactive nerve fibres in the developing salivary glands of the rat. Histochem (1992); 98: 317–325
   Google Scholar
• Yanase M., Kanosue K., Yasuda H., Tanaka H. Salivary secretion and grooming behaviour during heat exposure in freely moving rats. J. Physiol (1991); 432: 585–592
   PubMed Web of Science ®Google Scholar