1 The ability to manipulate pharmacologically pulmonary vascular tone
independent of effects on systemic blood vessels is a desirable object
ive. Elucidation of the biochemical mechanisms underlying hypoxia-indu
ced pulmonary vasoconstriction (HPV) may permit preferential targeting
of the pulmonary circulation. 2 Here we review our studies of the rol
e of locally synthesized candidate vasoactive factors in HPV. In addit
ion, we present data demonstrating an attenuated presser response to h
ypoxia in the pulmonary circulation of Fischer 344 rats compared with
the Wistar-Kyoto (WKY) rat strain. 3 We propose that a systematic geno
me-wide search using the HPV phenotype and a panel of highly informati
ve microsatellite markers will elucidate the genetic loci underlying t
he difference in susceptibility to HPV in these two rat strains and pr
ovide a valuable and novel insight into the factors that determine the
HPV response.