References
- Naclerio R M, Meier H L, Adkinson N F, Jr, et al. In vivo demonstration of inflammatory mediator release following nasal challenge with antigen. Eur J Respir Dis 1983; 64(Suppl 128)26–32
- Shaw R J, Fitzharris P, Cromwell O, Wardlaw A J, Kay A B. Allergen-induced release of sulphido-peptide leukotrienes (SRS-A) and LTB4 in allergic rhinitis. Allergy 1985; 40: 1–6
- Dolata J, Lindberg S, Mercke U. The effects of prostaglandins E1 E2 and F2α on mucociliary activity in the rabbit maxillary sinus. Acta Otolaryngol (Stockh) 1989; 108: 290–7
- Dolata J, Lindberg S, Mercke U. Histamine stimulates mucociliary activity in the rabbit maxillary sinus. Ann Otol Rhinol Laryngol, (in press)
- Coleridge H M, Coleridge J CG, Baker D G, Ginzel K H, Morrison M A. Comparison of the effects of histamine and prostaglandin on afferent C-fiber endings and irritant receptors in the intrapul-monary airways. Adv Exp Med Biol 1978; 99: 291–305
- Hahn R A, Patil P N. Further observations on the interaction of prostaglandin F2ä with cholinergic mechanisms in canine salivary glands. Eur J Pharmacol 1974; 25: 279–86
- Wasserman M A. Bronchopulmonary responses to prostaglandin F2α histamine and acetylcholine in the dog. Eur J Pharmacol 1975; 32: 146–55
- Secher C, Kirkegaard J, Borum P, Maansson A, Osterhammel P, Mygind N. Significance of H1 and H2 receptors in the human nose: rationale for topical use of combined antihistamine preparations. J Allergy Clin Immunol 1982; 70: 211–8
- Lundberg J M, Saria A. Capsaicin-induced desensitization of airway mucosa to cigarette smoke, mechanical and chemical irritants. Nature 1983; 302: 251–3
- Lindberg S, Dolata J, Mercke U. Stimulation of C fibers by ammonia vapor triggers a mucociliary defense reflex. Am Rev Respir Dis 1987; 135: 1093–8
- Lindberg S, Mercke U. Capsaicin stimulates mucociliary activity by releasing substance P and acetylcholine. Eur J Respir Dis 1986; 68: 96–106
- Hybbinette J C, Mercke U. A method for evaluating the effects of pharmacological substances on mucociliary activity in vivo. Acta Otolaryngol (Stockh) 1982; 93: 151–9
- Melville G N, Ismail S, Sealy C. Tracheobronchial function in health and disease. Respiration 1980; 40: 329–36
- Wanner A, Maurer D, Abraham W M, Szepfalusi Z, Sielczak M. Effects of chemical mediators of anaphylaxis on ciliary function. J Allergy Clin Immunol 1983; 72: 663–7
- Szolcsányi J. A pharmacological approach to elucidation of the role of different nerve fibres and receptor endings in mediation of pain. J Physiol (Paris) 1977; 73: 251–9
- Lindberg S, Dolata J, Mercke U. Effects of neurokinin A and calcitonin gene-related peptide on mucociliary activity in rabbit maxillary sinus. Regul Pept 1986; 16: 15–25
- Sundler F, Brodin E, Ekblad E, Hakanson R, Uddman R. Sensory nerve fibers: Distribution of substance P, neurokinin A and calcitonin gene related peptide. Tachykinin antagonists, R Häkanson, F Sundler. Elsevier Science Publishers B.V., Amsterdam 1985; 3–14
- Iravani J, Melville G N. Mucociliary activity in the respiratory tract as influenced by prostaglandin E1. Respiration 1975; 32: 305–15
- Richardson P S, Phipps R J, Balfre K, Hall R L. The roles of mediators, irritants and allergens in causing mucin secretion from the trachea. In: Respiratory tract mucus. Ciba Foundation Symposium 54 (new series). Elsevier/Excerpta Medica, Amsterdam 1978; 111–31
- Saria A, Martling C R, Yan Z, Theodorsson-Norheim E, Gamse R, Lundberg J M. Release of multiple tachykinins from capsaicin-sensitive sensory nerves in the lung by bradykinin, histamine, dimethylphenyl piperazinium, and vagal nerve stimulation. Am Rev Respir Dis 1988; 137: 1330–5