To evaluate the myogenic response and its ontogeny in large pulmonary arteries, we studied 45 newborn and 30 adult guinea pigs. Compared with the those of the adult, the newborn arterial vessels possessed a significantly @ < 0.01) smaller diameter (1153 ~t-34 versus 1656 5 65 km), static compliance (2.2 * 0.3 versus 4.6 * 0.7 pm/mN), and active stress (3.4 + 0.4 versus 5.8 ~t-0.7 mN/mm2). Stretchinduced contraction was obtained by quick stretch of the vessel segments to 120, 140, 160, 180, or 200% of their optimal length, and the myogenic response was measured as the change in force after muscle relaxation with papaverine. A myogenic response was observed in 94% of the newborn and 93% of adult vessel segments, and significant age differences in the response were present. The magnitude of the active force generated for any stretch over 120% was significantly greater in the newborn (p < 0.01), and as a percentage of K+ (127 mM) stimulation, a 2-fold Vessels respond to an increase in intraluminal pressure with vasoconstriction. This phenomenon, called the myogenic response or stretch-induced contraction, was originally described by Bayliss in 1902 (1). Previous data on in vitro vessel segments and in vivo organ perfusion studies of several animal species have confirmed its existence in a variety of systemic vessels (2-7). The phenomenon is most prevalent in small resistance units, and this has led to the current belief that the myogenic response plays an important role in organ autoregulation of blood flow after arterial pressure changes (2).Limited data are available on the myogenic response of lung vessels. In pulmonary allografts in the hamster, Davis et al. (8) were unable to observe any changes in arteriolar diameter after alterations in transmural pressure, whereas vasoconstriction was observed in systemic cheek pouch arterioles under similar conditions. T o the best of our knowledge, the only other study of the myogenic response in pulmonary vessels was reported by