In adult animals, the upper airway (UA) has been shown to contain receptors sensitive to UA cooling [1][2][3][4][5]. The application of cool air to the isolated UA inhibits breathing [6][7][8][9] and this effect is abolished by laryngeal anaesthesia [6] or by cutting the superior laryngeal nerves [7][8][9]. UA cooling has also been shown to modify UA dilator muscle activity [7][8][9][10][11] and this effect was also abolished by superior laryngeal nerve section [7,9,11]. In adult rats, moderate UA cooling has been shown to increase UA dilator muscle activity and reduce UA resistance [8,9], suggesting that changes in UA temperature may play a role in the control of UA patency.The effects of UA cooling on UA muscle activity and UA resistance have not been investigated in young animals. Little is known about UA receptors in young animals, although superior laryngeal nerve afferents responding to UA pressure, airflow, UA movement and/or muscle activity have been described in neonatal dogs [12] and to water in neonatal dogs [13] and neonatal sheep, cats and monkeys [14]. UA cooling has been shown to inhibit breathing in neonatal dogs [15] and guinea-pigs [16] and possibly in neonatal cats [17], and these effects were abolished by laryngeal anaesthesia [17] or superior laryngeal nerve section [15,16]. Menthol, a specific cold receptor stimulant, also inhibits breathing in neonatal dogs [18]. It has been suggested that the ventilatory depression caused by cooling and laryngeal reflex responses to water is greater in neonates than in adults [12,13,17].The purpose of the present study was to examine the effects of UA cooling on UA dilator muscle activity and on UA resistance in young guinea-pigs. The young guineapig is known to be neurologically more mature than several other species [19]. However, it has been shown previously that UA reflex responses are very different in 10-14-day-old compared with adult guinea-pigs [20]. There are also maturational differences in local airway responses, since exsanguination-induced bronchoconstriction has been shown to be greater in 15-day-old than in adult guineapigs [21].
Materials and methodsThe procedure for isolation of the UA has been described previously [16]. In brief, 17 young guinea-pigs (Biological Laboratories Europe Ltd., Carrentrila, Ireland) aged 15.7±0.4 days with a body weight of 197.8±7.3 g (mean±SD) were anaesthetised using urethane (2 g·kg -1 i.p.) and placed supine on a thermostatically controlled heating pad to maintain body temperature at 37°C. The fur was removed from the ventral aspect of the neck and a midline incision was made, exposing the trachea. With the aid of a binocular microscope (Leica, Wild MC3, Heerbrugg, Switzerland) a low cervical tracheostomy was performed through which the animal could breathe spontaneously. Tracheal airflow was continuously recorded using a heated pneumotachograph (Hans Rudolph, KS, USA) and differential pressure transducer (Validyne DP 15, North Ridge, CA, USA) placed in series with the tracheal cannula and the signal was in...