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Cardiovascular responses to serotonin in experimental liver disease
Author(s) -
Jacob Giris,
Bishara Bashara,
Lee Samuel S.,
Hilzenart Nir,
Bomzon Arieh
Publication year - 1991
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.1840140645
Subject(s) - serotonin , medicine , disease , cardiology , receptor
Recent evidence suggests that serotonergic mechanisms within the cardiovascular system are activated and may be important in the development of the hyperkinetic circulation and the maintenance of portal hypertension in cirrhotic patients. The in vivo pressor and positive chronotropic response together with the in vitro contractile responses of aortic rings and portal veins to serotonin were studied in three different rat models of cirrhosis, portal hypertension and jaundice: the portal vein–ligated rat, the carbon tetrachloride–induced cirrhotic rat, the chronic bile duct–ligated cirrhotic rat and the 3‐day noncirrhotic, nonportal hypertensive–jaundiced rat. In addition, the activity of the enzyme monoamine oxidase type A was determined in lung homogenates prepared from the four groups of sham and treated animals. In the four different groups of sham‐treated or operated pithed rats, serotonin caused a dose‐dependent increase in mean arterial blood pressure without any effect on the heart rate. The pressor responses to serotonin in the three models of portal hypertension were significantly attenuated from their respective sham group. In the 3‐day noncirrhotic, nonportal hypertensive–jaundiced rats, the pressor response was no different than that seen in the sham‐operated rats. No evidence of consistent potentiated or blunted in vitro reactivity to serotonin of arterial rings and portal veins from the four groups of rats was seen. Portal hypertension, cirrhosis and hyperbilirubinemia had no effect on the activity of monoamine oxidase type A. These data demonstrate that portal hypertension is associated with an attenuated pressor response to serotonin. The mechanism of this attenuated response is not linked to altered in vitro reactivity of arterial rings to serotonin or increases in the activity of pulmonary monoamine oxidase. Because the in vitro reactivity of portal veins from portal hypertensive rats was not hypersensitive to serotonin, our data are consistent with the proposal that serotonin 2 ‐antagonists exert their portal hypotensive action by lowering resistance in the mesenteric and collateral circulation of cirrhotic patients. (H EPATOLOGY 1991;14:1235–1242).