Effects of capsaicin pretreatment on expiratory laryngeal closure during pulmonary edema in lambs.

The present study, performed in nonsedated, conscious lambs, consisted of two parts. In the first part, we 1) examined for the first time whether a respiratory response to pulmonary C-fiber stimulation could be elicited in nonsedated newborns and 2) determined whether this response could be abolished by capsaicin pretreatment. Then, by using capsaicin-desensitized lambs, we studied whether pulmonary C fibers were involved in the sustained, active expiratory upper airway closure previously observed during pulmonary edema. Airflow and thyroarytenoid and inferior pharyngeal constrictor muscle electromyographic activities were recorded. In the first set of experiments, a 5-10 microg/kg capsaicin bolus intravenous injection in seven intact lambs consistently led to a typical pulmonary chemoreflex, showing that C fibers are functionally mature in newborn lambs. In the second series of experiments, eight lambs pretreated with 25-50 mg/kg subcutaneous capsaicin did not exhibit any respiratory response to 10-50 microg/kg intravenous capsaicin injection, implicating C fibers in the response. Finally, in the above capsaicin-desensitized lambs, we observed that halothane-induced high-permeability pulmonary edema did not cause the typical response of sustained expiratory upper airway closure seen in the intact lamb. We conclude that functionally mature C fibers are present and responsible for a pulmonary chemoreflex in response to capsaicin intravenous injection in nonsedated lambs. Capsaicin pretreatment abolishes this reflex. Furthermore, the sustained expiratory upper airway closure observed during halothane-induced pulmonary edema in intact nonsedated lambs appears to be related to a reflex involving stimulation of pulmonary C fibers.     

Vagal afferents and active upper airway closure during pulmonary edema in lambs.

The present study was undertaken to gain further insight into the mechanisms responsible for the sustained active expiratory upper airway closure previously observed during high-permeability pulmonary edema in lambs. The experiments were conducted in nonsedated lambs, in which airflow and thyroarytenoid and inferior pharyngeal constrictor muscle electromyographic activity were recorded. We first studied the consequences of hemodynamic pulmonary edema (induced by impeding pulmonary venous return) on upper airway dynamics in five lambs; under this condition, a sustained expiratory upper airway closure consistently appeared. We then tested whether expiratory upper airway closure was related to vagal afferent activity from bronchopulmonary receptors. Five bivagotomized lambs underwent high-permeability pulmonary edema: no sustained expiratory upper airway closure was observed. Finally, we studied whether a sustained decrease in lung volume induced a sustained expiratory upper airway closure. Five lambs underwent a 250-ml pleural infusion: no sustained expiratory upper airway closure was observed. We conclude that 1) the sustained expiratory upper airway closure observed during pulmonary edema in nonsedated lambs is related to stimulation of vagal afferents by an increase in lung water and 2) a decrease in lung volume does not seem to be the causal factor.     

Coordination between glottic adductor muscle and diaphragm EMG activity in fetal lambs in utero

It haspreviously been reported that active glottic adduction is presentduring prolonged apneas but absent during periods of breathingmovements in fetal lambs in utero. The present study was aimed atexamining the precise coordination between fetal breathing movements[diaphragm electromyographic (EMG) activity (Di EMG)] andglottic adduction [thyroarytenoid muscle EMG activity (TAEMG)]. Electrodes for electroencephalogram, eye movements, TAEMG, and Di EMG and an arterial catheter were surgically implanted infetal lambs 123-142 days postconception. Polygraphic recordings were performed without sedation while the ewe breathed room air (n = 11) or various gas mixtures(hypoxia, n = 5; hyperoxia,n = 4; hypercapnia,n = 5; hypercapnia+hyperoxia,n = 5). Tonic TA EMG was observedthroughout >90% of apneas (>6 s) in both non-rapid-eye-movement and rapid-eye-movement sleep, and when Di EMG frequency decreased inrapid-eye-movement sleep. In all but two fetuses, TA EMG was immediately inhibited when Di EMG appeared. Altering blood gases did not modify these results. In conclusion, Di EMG and TAEMG are well coordinated in late gestation in fetal lambs,except in a few cases. These findings may have consequencesfor understanding the pathogenesis of mixed/obstructiveapneas of prematurity.

     

Evolutionary conservation of drug action on lipoprotein metabolism-related targets

Genetic analysis has shown that the slower than normal rhythmic defecation behavior of the clk-1 mutants of Caenorhabditis elegans is the result of altered lipoprotein metabolism. We show here that this phenotype can be suppressed by drugs that affect lipoprotein metabolism, including drugs that affect HMG-CoA reductase activity, reverse cholesterol transport, or HDL levels. These pharmacological effects are highly specific, as these drugs affect defecation only in clk-1 mutants and not in the wild-type and do not affect other behaviors of the mutants. Furthermore, drugs that affect processes not directly related to lipid metabolism show no or minimal activity. Based on these findings, we carried out a compound screen that identified 190 novel molecules that are active on clk-1 mutants, 15 of which also specifically decrease the secretion of apolipoprotein B (apoB) from HepG2 hepatoma cells. The other 175 compounds are potentially active on lipid-related processes that cannot be targeted in cell culture. One compound, CHGN005, was tested and found to be active at reducing apoB secretion in intestinal Caco-2 cells as well as in HepG2 cells. This compound was also tested in a mouse model of dyslipidemia and found to decrease plasma cholesterol and triglyceride levels. Thus, target processes for pharmacological intervention on lipoprotein synthesis, transport, and metabolism are conserved between nematodes and vertebrates, which allows the use of C. elegans for drug discovery.     

Inferior pharyngeal constrictor electromyographic activity during permeability pulmonary edema in lambs

Diaz, Véronique, Irenej Kianicka, PatrickLetourneau, and Jean-Paul Praud. Inferior pharyngealconstrictor electromyographic activity during permeability pulmonaryedema in lambs. J. Appl. Physiol. 81(4): 1598-1604, 1996.Newborn mammals exhibit an active expiratory upper airwayclosure during the first hours of extrauterine life. We have recentlyshown that permeability pulmonary edema led to active expiratoryglottic closure in awake newborn lambs while hypoxia (inspiredO₂ fraction 8%; 15 min) did not. In the presentstudy, we tested the hypothesis that expiratory glottic closure wasaccompanied by an increase in pharyngeal constrictor muscle expiratoryelectromyographic (EMG) activity. We studied seven awake nonsedatedlambs aged 8-20 days. Airflow (facial mask + pneumotachograph),blood gases (arterial catheter), and EMG activity of both thethyroarytenoid muscle (a glottic adductor) and the inferior pharyngealconstrictor muscle were recorded before and after intravenous injectionof halothane (0.05 ml/kg) to induce a permeability pulmonary edema. Acentral apnea (duration 15 s to 5 min) with continuous thyroarytenoidand inferior pharyngeal constrictor activity was observed withinseconds after halothane injection. One lamb died despite rescuingmaneuvers. An expiratory phasic thyroarytenoid and inferior pharyngealconstrictor muscle activity with simultaneous zero airflow graduallytook place and, by 30 min after halothane injection, was present ateach expiration in the six remaining lambs. Expiratory glottic andpharyngeal constrictor muscle EMG activity was subsequently presentduring the whole study period (1.5-5 h), even after correction ofthe initial hypoxia. Permeability lung edema was present at postmortem examination in all seven lambs. We conclude that a permeability pulmonary edema induced by intravenous halothane in nonsedated lambsenhances both glottic and pharyngeal constrictor muscle expiratory EMG.We hypothesize that expiratory contraction of the inferior pharyngealconstrictor muscle could participate in the active expiratory upperairway closure; this, in turn, might improve alveolocapillary gasexchange by increasing the end-expiratory lung volume.

     

Laryngeal and abdominal muscle electrical activity during periodic breathing in nonsedated lambs

Kianicka, Irenej, Véronique Diaz, Sylvain Renolleau,Emmanuel Canet, and Jean-Paul Praud. Laryngeal and abdominal muscle electrical activity during periodic breathing in nonsedated lambs. J. Appl. Physiol. 84(2):669-675, 1998.We recently reported that glottic closure waspresent throughout central apneas in awake lambs. The present studytested whether glottic closure was also observed during periodicbreathing (PB). We attempted to induce PB in 21 nonsedated lambs onreturn from hypocapnic hypoxia to room air. Airflow and thyroarytenoid(a laryngeal constrictor, n = 16),cricothyroid (a laryngeal dilator, n = 10), and abdominal (n = 9) muscleelectrical activity (EMG) were monitored continuously. PB was observedin 16 lambs, with apneic phases in 8 lambs. Thyroarytenoid muscle EMGwas observed at the nadir of PB, either throughout apnea or withprolonged expiration during the lowest respiratory efforts. Phasicinspiratory cricothyroid muscle EMG and phasic expiratory abdominal EMGdisappeared at the nadir of PB. Active glottic closure at the nadir ofPB, without abdominal muscle contraction, could be a beneficialmechanism, preserving alveolar gas stores for continuing gas exchangeduring the apneic/hypopneic phase of PB. However, consequences ofactive glottic closure on ventilatory instability, either enhancing orreducing, are unknown.