Abstract
Endothelin (ET) mechanisms were studied in hyper-and hypo-thyroid states in rats. Hyperthyroidism was induced by daily administration of thyroxine (0.1 mg/kg, i.p.) for 8 weeks, while hypothyroidism was induced by daily administration of methimazole (10 mg/kg, i.p.) for 8 weeks. The concentration of endogenous ET-1 was determined in the kidneys using radioimmunoassay. Systemic hemodynamics and renal blood circulation was measured using a radioactive microsphere technique. A significant increase in systolic and diastolic blood pressure, heart rate and cardiac output was observed in hyperthyroid rats as compared to eu- and hypo-thyroid rats. Total peripheral resistance was found to be similar in eu-, hyper- and hypo-thyroid rats. The endogenous concentration of ET-1 in the kidneys was significantly lower in hyper- as compared to eu- and hypo-thyroid rats. The blood flow to the kidneys was significantly increased in hyper- as compared to eu- and hypothyroid rats. Infusion of ET-1 (100 ng/kg/min i.v. for 45 min) produced a significant decrease in blood flow to the kidneys of eu-, hyper- and hypo-thyroid rats. The decrease in blood flow was similar in eu-, hyper- and hypo-thyroid rats, indicating that the response of renal blood vessels to exogenous ET-1 is not altered during thyroid dysfunction. Since endogenous ET-1 is involved in the regulation of vascular tone, it may be concluded that in hyper-thyroid rats decrease in concentration of the renal ET-1 could be contributing to an increase in blood flow to the kidney. © 1994.
Original language | American English |
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Journal | Life Sciences |
Volume | 54 |
State | Published - Jan 1 1994 |
Keywords
- Animal
- Animalia
- ET-1-like immunoreactivity
- Endothelins
- Kidney
- Methimazole
- Rats
- Renal Circulation
- Sprague-Dawley
- animal experiment
- animal model
- animal tissue
- article
- blood vessel tone
- controlled study
- diastolic blood pressure
- endothelin 1
- heart output
- heart rate
- hemodynamics
- hyperthyroidism
- hypothyroidism
- intracardiac drug administration
- intraperitoneal drug administration
- intravenous drug administration
- kidney blood flow
- male
- microsphere sc 46
- microsphere sn 113
- nonhuman
- rat
- renal blood flow
- systolic blood pressure
- thiamazole
- thyroxine
- tissue level
- vascular resistance
Disciplines
- Medicine and Health Sciences