Decreased pulmonary vascular resistance during nasal breathing: modulation by endogenous nitric oxide from the paranasal sinuses

被引:39
作者
Settergren, G
Angdin, M
Astudillo, R
Gelinder, S
Liska, J
Lundberg, JON
Weitzberg, E
机构
[1] Karolinska Inst, Karolinska Hosp, Dept Surg Sci, Div Cardiothorac Anaesthet & Insens Care, Stockholm, Sweden
[2] Karolinska Inst, Karolinska Hosp, Dept Surg Sci, Div Thorac Surg, Stockholm, Sweden
[3] Karolinska Inst, Karolinska Hosp, Dept Physiol & Pharmacol, Stockholm, Sweden
[4] Karolinska Inst, Karolinska Hosp, Dept Surg Sci, Div Anesthesiol & Intens Care, Stockholm, Sweden
来源
ACTA PHYSIOLOGICA SCANDINAVICA | 1998年 / 163卷 / 03期
关键词
nitric oxide; paranasal sinuses; pulmonary vascular resistance;
D O I
10.1046/j.1365-201x.1998.00352.x
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Nitric oxide is present in high concentration in the human nasal airways. During inspiration through the nose a bolus is transported to the lungs. In a randomized cross-over study the effect of two different patterns of breathing, nasal breathing and mouth breathing, was evaluated in 10 patients (mean age 65 years), breathing room air the morning of the first post-operative day after open heart surgery. Nasal breathing is defined as inspiration through the nose and expiration through the mouth. whilst mouth breathing is the converse of this: inspiration through the mouth and expiration through the nose. Pressure in the pulmonary artery and left atrium or pulmonary artery wedge was measured together with thermodilution cardiac output and arterial and mixed venous oxygenation and acid-base parameters. Pulmonary vascular resistance index (PVRI), venous admixture and alveolar-arterial gradient were calculated. Nasal breathing resulted in a lower PVRI. 256 dyn s cm(-5) cm(-2) vs. 287 (P < 0.01). The oxygen and carbon dioxide tension and pH of arterial and mixed venous blood, venous admixture and the alveolar-arterial gradient remained unchanged. The decreased level of PVRI during nasal breathing compared to that during mouth breathing supports the notion, that endogenous nitric oxide acts as an airborne messenger to modulate the pulmonary vascular tone during normal breathing.
引用
收藏
页码:235 / 239
页数:5
相关论文
共 16 条
[1]  
ALVING K, 1993, EUR RESPIR J, V6, P1368
[2]   AUTOINHALATION OF NITRIC-OXIDE AFTER ENDOGENOUS SYNTHESIS IN NASOPHARYNX [J].
GERLACH, H ;
ROSSAINT, R ;
PAPPERT, D ;
KNORR, M ;
FALKE, KJ .
LANCET, 1994, 343 (8896) :518-519
[3]   TIME-COURSE AND DOSE-RESPONSE OF NITRIC-OXIDE INHALATION FOR SYSTEMIC OXYGENATION AND PULMONARY-HYPERTENSION IN PATIENTS WITH ADULT-RESPIRATORY-DISTRESS-SYNDROME [J].
GERLACH, H ;
ROSSAINT, R ;
PAPPERT, D ;
FALKE, KJ .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1993, 23 (08) :499-502
[4]  
HOGMAN M, 1997, COMMUNICATION
[5]  
KELLY KP, 1996, INTENS CARE MED, V22, P137
[6]   RESISTANCE OR CONDUCTANCE FOR EXPRESSION OF ARTERIAL VASCULAR TONE [J].
LAUTT, WW .
MICROVASCULAR RESEARCH, 1989, 37 (02) :230-236
[7]   Nitric oxide, produced in the upper airways, may act in an 'aerocrine' fashion to enhance pulmonary oxygen uptake in humans [J].
Lundberg, JON ;
Lundberg, JM ;
Settergren, G ;
Alving, K ;
Weitzberg, E .
ACTA PHYSIOLOGICA SCANDINAVICA, 1995, 155 (04) :467-468
[8]   PRIMARILY NASAL ORIGIN OF EXHALED NITRIC-OXIDE AND ABSENCE IN KARTAGENERS-SYNDROME [J].
LUNDBERG, JON ;
WEITZBERG, E ;
NORDVALL, SL ;
KUYLENSTIERNA, R ;
LUNDBERG, JM ;
ALVING, K .
EUROPEAN RESPIRATORY JOURNAL, 1994, 7 (08) :1501-1504
[9]   Inhalation of nasally derived nitric oxide modulates pulmonary function in humans [J].
Lundberg, JON ;
Settergren, G ;
Gelinder, S ;
Lundberg, JM ;
Alving, K ;
Weitzberg, E .
ACTA PHYSIOLOGICA SCANDINAVICA, 1996, 158 (04) :343-347
[10]   NASALLY EXHALED NITRIC-OXIDE IN HUMANS ORIGINATES MAINLY IN THE PARANASAL SINUSES [J].
LUNDBERG, JON ;
RINDER, J ;
WEITZBERG, E ;
LUNDBERG, JM ;
ALVING, K .
ACTA PHYSIOLOGICA SCANDINAVICA, 1994, 152 (04) :431-432