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Diaspirin crosslinked hemoglobin (DCLHb): control of pressor effect with anti-hypertensive agents
Insights
Diaspirin crosslinked hemoglobin (DCLHb) increases blood pressure. This study found that common antihypertensive drugs effectively controlled the pressor effect of DCLHb in rats.
Area of Science:
- Pharmacology
- Cardiovascular Physiology
Background:
- Diaspirin crosslinked hemoglobin (DCLHb) is a blood substitute that can elevate mean arterial pressure (MAP).
- Managing the pressor effects of DCLHb is crucial for its clinical application.
Purpose of the Study:
- To investigate the efficacy of common antihypertensive agents in controlling the pressor effect of DCLHb.
- To assess the impact of these agents on heart rate (HR) in conjunction with MAP control.
Main Methods:
- Awake rats received an intravenous injection of DCLHb (280 mg/kg).
- Subsequently, rats were treated with prazosin, nitroglycerine (NTG), nicardipine, or labetalol.
- Mean arterial pressure (MAP) and heart rate (HR) were monitored throughout the experiment.
Main Results:
- All tested antihypertensive agents (prazosin, NTG, nicardipine, labetalol) promptly restored elevated MAP to baseline levels.
- Prazosin and NTG normalized HR, while nicardipine and labetalol resulted in persistent bradycardia.
- The findings indicate that DCLHb-induced hypertension is manageable with various drug classes.
Conclusions:
- The pressor effect of Diaspirin crosslinked hemoglobin can be effectively managed using widely available antihypertensive medications.
- Different classes of antihypertensives exhibit varying effects on heart rate when counteracting DCLHb-induced hypertension.
Abstract:
Diaspirin crosslinked hemoglobin (DCLHb) administration elevates mean arterial pressure (MAP). The purpose of this study was to determine whether commonly used antihypertensive agents could control this pressor effect in rats. Awake rats were injected intravenously (i.v.) with 280 mg/kg of DCLHb. Fifteen minutes later when MAP was 25-30% above baseline and heart rate (HR) was reciprocally decreased, prazosin (2 mg/kg;an alpha adrenergic blocker), nitroglycerine (NTG; 10-150 mcg/min; a nitrovasodilator), nicardipine (0.204-0.08 mg/hr; a calcium channel blocker) or labetalol (5 mg/kg; an alpha/beta adrenergic blocker) was administered i.v. All four classes of antihypertensive agents promptly restored MAP to baseline. Coincident with the return of MAP to baseline, HR was restored to baseline in prazosin and NTG treated animals, however, bradycardia persisted in those animals treated with nicardipine and labetalol, most likely due to the negative chronotropic properties of these agents. We conclude that the pressor effect of DCLHb can be readily controlled with at least four different classes of commonly used antihypertensive agents.
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