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Since the discovery of prostacyclin (PGI2) in 1976, there has been great interest in its vascular effects and potential clinical applications. High infusion rates of PGI2 markedly depress arterial blood pressure both in animal studies and in clinical trials. This fall in pressure may result entirely from a decrease in arterial resistance. However, it is possible that the administration of PGI2 may decrease ventricular filling due to an increase in vascular capacity. To investigate whether or not PGI2 affects vascular capacity, we infused PGI2 intraarterially at both 10 and 25 micrograms/min into 15 dogs on total cardiopulmonary bypass. These infusions were associated with a 25 +/- 3 mmHg decrease in arterial pressure and an increase in vascular capacity of 155 +/- 29 ml (SE, P less than 0.005). This increase in capacity was greater (P less than 0.02) than the increase of 23 +/- 42 ml resulting from infusions of nitroglycerin into eight dogs at 2 mg/min, which produced a decrease in arterial pressure of 23 +/- 4 mmHg, which was the maximal effect that could be achieved. Neither bilateral cervical vagotomy nor beta adrenergic blockade with propranolol significantly diminished the increase in vascular capacity associated with infusions of PGI2. The results from studies in four eviscerated dogs indicated that PGI2 acts on both splanchnic and extrasplanchnic capacity vasculature. To compare the direct effects of PGI2 with those of nitroglycerin and nitroprusside on venous tone, we used an isolated canine spleen preparation. Infusions of PGI2 (100 mcg/min) increased spleen weight in this preparation by 9.0 +/- 2.4% (n = 10, P less than 0.001); this increase was significantly greater than increases of 3.6 +/- 2.2% (P less than 0.001) and 3.5 +/- 2.3% (P less than 0.001) caused by high dose infusions of nitroglycerin (1 mg/min) and nitroprusside (400 micrograms/min), respectively. Thus, PGI2 substantially increases vascular capacity by a mechanism that appears to involve a direct action on vascular smooth muscle. Furthermore, these results suggest that PGI2 might be useful in clinical conditions in which an increase in vascular capacity is indicated.
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
July 1981,
The Journal of clinical investigation,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
January 1982,
The Journal of clinical investigation,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
November 1976,
Circulation research,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
January 1980,
Circulation research,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
March 1987,
The Annals of thoracic surgery,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
January 1978,
VASA. Zeitschrift fur Gefasskrankheiten,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
October 1982,
Pharmacological research communications,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
April 1986,
Arzneimittel-Forschung,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
November 1983,
Thrombosis research,
T G Fulghum, and
J P DiMarco, and
E W Supple, and
I Nash, and
J Gendlerman, and
D F Eton, and
J B Newell, and
R M Zusman, and
W J Powell
August 1980,
Canadian journal of physiology and pharmacology,
