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Antihypertensive effect of interleukin-2.
1Masonic Medical Research Laboratory, Utica, New York 13501-1787.
Hypertension (Dallas, Tex. : 1979)
|January 1, 1990
Summary
Interleukin-2 administration effectively lowers blood pressure in spontaneously hypertensive rats, offering a potential new therapeutic avenue for hypertension. This T cell growth factor demonstrated sustained antihypertensive effects without apparent toxicity.
Area of Science:
- Immunology
- Cardiovascular Science
- Pharmacology
Background:
- Cyclooxygenase inhibitors like aspirin may increase interleukin-2 release from T cells.
- Aspirin has demonstrated antihypertensive effects in spontaneously hypertensive rats (SHR).
- SHR models are reportedly T cell deficient, prompting investigation into T cell factors.
Purpose of the Study:
- To investigate the effect of interleukin-2 (IL-2) on hypertension in the spontaneously hypertensive rat (SHR) model.
- To determine if IL-2 can alter the course of hypertension in SHR.
- To assess the duration and safety of IL-2 treatment in hypertensive rats.
Main Methods:
- Administration of a single bolus of interleukin-2 (5,000 units/kg s.c.) to young and adult spontaneously hypertensive rats.
- Monitoring of blood pressure in treated SHR.
- Assessment of blood pressure in Goldblatt, single-kidney wistar-kyoto rats following IL-2 administration.
Main Results:
- A single dose of IL-2 prevented hypertension onset in young SHR.
- IL-2 lowered blood pressure to normotensive levels in adult SHR.
- The antihypertensive effect persisted for at least 6 months with no observed toxicity.
- IL-2 did not affect blood pressure in a renal hypertension model (Goldblatt rats).
Conclusions:
- Interleukin-2 has significant and long-lasting antihypertensive effects in the spontaneously hypertensive rat model.
- IL-2 may represent a novel therapeutic strategy for essential hypertension.
- The effects of IL-2 appear specific to the SHR model and not generalized to renal hypertension.