Abstract |
The rabbit epigastric free flap was used to investigate the effect of prostacyclin and drugs modifying its synthesis in vivo on microvascular blood flow. Prostacyclin and its analogue carbacyclin caused an increase in flow with a maximal twofold increase at approximately 6.5 and 250 ng/ml, respectively, in the flap. Thromboxane synthetase inhibitors such as dazoxiben hydrochloride, UK-38,485, 7-IHA, and imidazole (up to 7 X 10(-4) M in the flap) as well as the prostaglandins 6-oxo-PGF1 alpha and PGE2 (up to 3.7 and 9.2 ng/ml, respectively, in the flap) all failed to modify the control flow rate in the cutaneous microcirculation. It is concluded that the vasodilatory properties of prostacyclin and carbacyclin, together with their known platelet antiaggregatory properties, warrant further study in problem areas of microsurgery such as flap ischemia. The use of thromboxane synthetase inhibitors had no demonstrable effect on the normal flap, and their effect on the ischemic flap remains to be investigated.
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Authors | K R Knight, D J Crabb, M Niall, J A Angus, T J Martin, B M O'Brien |
Journal | Plastic and reconstructive surgery
(Plast Reconstr Surg)
Vol. 75
Issue 5
Pg. 692-702
(May 1985)
ISSN: 0032-1052 [Print] United States |
PMID | 3157201
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cyclooxygenase Inhibitors
- Imidazoles
- Pyrazoles
- Pyrazolones
- dazmegrel
- 6-Ketoprostaglandin F1 alpha
- carboprostacyclin
- imidazole
- Epoprostenol
- Thromboxane-A Synthase
- nafazatrom
- Indomethacin
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Topics |
- 6-Ketoprostaglandin F1 alpha
(pharmacology)
- Abdominal Muscles
(blood supply)
- Animals
- Blood Flow Velocity
- Blood Pressure
(drug effects)
- Cyclooxygenase Inhibitors
- Epoprostenol
(pharmacology)
- Imidazoles
(pharmacology)
- Indomethacin
(pharmacology)
- Microcirculation
(drug effects)
- Platelet Aggregation
(drug effects)
- Pyrazoles
(pharmacology)
- Pyrazolones
- Rabbits
- Regional Blood Flow
(drug effects)
- Surgical Flaps
- Thromboxane-A Synthase
(antagonists & inhibitors)
- Vasoconstriction
(drug effects)
- Vasodilation
(drug effects)
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