“…The anatomical similarities of the mammalian pulmonary vasculature and the gill, i.e., both receive the entire cardiac output and have extensive endothelial (or pillar) cell surface area, has prompted an investigation into the ability of gill vessels to also "condition" plasma prior to systemic perfusion. Recent studies have indicated that the gill vasculature has attributes similar to the lung; i.e., it activates angiotensin I1 and extracts andlor metabolizes adenosine, catecholamines, serotonin, and bradykinin, and products of the arachidonic acid cascade (Colin and Leray, 1979;Colletti and Olson, 1988;Galardy et al, 1984;Hemker, 1987;Kullman and Olson, 1989;Lipke and Olson, 1988;Nekvasil and Olson, 1986;Olson et al, 198613;. However, unlike the pulmonary circulation, which is a single pass perfusion, blood perfusing the gill may pass through one (arterioarterial) or two (arterioarterial plus arteriovenous) microvascular networks.…”