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Journal ArticleDOI

Selective Passage of Prostaglandins across the Lung

TLDR
The removal of prostaglandins by the lung restricts their activities to the organs from which they are released and between their organ of origin and the site in the pulmonary circulation where they are inactivated.
Abstract
STIMULATION of the splenic nerves releases prostaglandins from the spleen to give concentrations of as much as 0.2 µg/ml. in splenic venous blood1. The release of prostaglandins might influence organs remote from the site of release, for prostaglandins can exert potent actions on smooth muscle2. The lung has recently been shown to determine the fate of many vasoactive substances; some are activated—conversion of angiotensin I to angiotensin II (ref. 3)—and some inactivated. The degree of inactivation seems to be specific for a given substance, ranging from almost complete (bradykinin4, 5-hydroxytryptamine5, prostaglandins E1 E2 and F2α (ref. 1)), to minor (noradrenaline6), to allowance of their free passage (adrenaline6 and angiotensin II (ref. 7)). The removal of prostaglandins by the lung restricts their activities to the organs from which they are released and between their organ of origin and the site in the pulmonary circulation where they are inactivated1. A prostaglandin which passed through the lungs after its release from an organ could be considered a circulating hormone, as long as it is not rapidly degraded in the blood. Ferreira and Vane1 reported that prostaglandins E1 E2 and F2α were stable in blood, though rapidly inactivated by the lung. Removal of prostaglandins A1 and A2 by the lung was not determined because the assay organs are insensitive to them. Vascular smooth muscle, however, unlike other smooth muscle, is reactive to low concentrations of prostaglandins A1 and A2 (refs. 8–10) and the renal vasculature is probably most sensitive to prostaglandins A1 and A2 (refs. 10 and 11). Because the renal vasculature is also sensitive to prostaglandins E1 and E2 (ref. 12), it has been used as an index of the fate of prostaglandins infused into the venous and arterial circulations.

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Citations
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Journal ArticleDOI

Prostaglandins and thromboxanes.

TL;DR: This chapter discusses major advances in prostaglandin chemistry and biological activity and indicates the extent to which research has progressed towards the realization of earlier hopes of the discovery of new therapeutic agents.
Journal ArticleDOI

Inactivation of Prostaglandins by the Lungs

TL;DR: Prostaglandins E1, E2, F2α and A2 are enzymically inactivated to different extents during passage through the pulmonary circulation and the enzyme responsible is probably 15-hydroxyprostaglandsin dehydrogenase.
Journal ArticleDOI

Radioimmunoassay measurement of prostaglandins E, A, and F in human plasma.

TL;DR: The details of a radioimmunoassay capable of measuring as 5 pg of prostaglandin A, E, and F (PGA, PGE, and PGF) in human and rat plasma are described and appears to be of considerable experimental as well as clinical interest.
Journal ArticleDOI

Identification and characterization of a prostaglandin transporter

TL;DR: The protein encoded by the matrin F/G complementary DNA is preferably called PGT because it is likely to function as a prostaglandin transporter.
Journal ArticleDOI

Release of a Prostaglandin E-Like Substance from Canine Kidney by Bradykinin

TL;DR: Results suggest that a prostaglandin E-like substance participates in the renal vasodilator and the diuretic responses to bradykinin, which is correlated with changes in renal venous concentrations of substances having the properties of prostag landins of the E and F series in anesthetized dogs.
References
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Journal ArticleDOI

Prostaglandins: Their Disappearance from and Release into the Circulation

TL;DR: The liver and lungs provide an efficient protective mechanism to remove almost all the prostaglandin before it reaches the arterial circulation.
Journal Article

The prostaglandins: a family of biologically active lipids

TL;DR: The prostaglandins are a family of lipids, originally discovered over 30 years ago in human seminal fluid, which have since been found not only to have a wide variety of striking pharmacological actions, but also to be present in many if not all mammalian tissues.
Journal ArticleDOI

Conversion of angiotensin I to angiotensin II.

TL;DR: Results obtained with the blood bathed organ technique indicate that angiotensin I is converted rapidly to angiotENSin II in the pulmonary circulation and not by an enzyme in the blood.
Journal ArticleDOI

Prostaglandins released by the Spleen

TL;DR: Experiments with dogs have shown that both prostaglandin E2 and F2α are released when the spleen is contracted by nerve stimulation or by adrenaline.
Journal ArticleDOI

The use of isolated organs for detecting active substances in the circulating blood. 1964.

TL;DR: In this paper, a method is described for the assay of circulating hormones after their injection or release into the circulation, which is applicable to cats, dogs and rabbits, and consists of bathing or superfusing isolated smooth muscle preparations in a stream of heparinized arterial blood.
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