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Updated: Jun 24, 2026

Developing a Clinically Relevant Hemorrhagic Shock Model in Rats
Published on: March 22, 2024
Effects of carvedilol on mortality and inflammatory responses to severe hemorrhagic shock in rats
Takumi Taniguchi1, Akihide Kurita, Ken Yamamoto
1Department of Emergency and Critical Care Medicine, Graduate School of Medical Science, Kanazawa University, Japan. takutaniyan@yahoo.co.jp
Insights
Carvedilol, a common heart medication, worsened outcomes in rats experiencing severe hemorrhagic shock, increasing mortality and inflammation. This suggests potential risks when using carvedilol in shock patients.
Area of Science:
- Pharmacology
- Critical Care Medicine
- Physiology
Background:
- Carvedilol is a beta-blocker and alpha-blocker used for hypertension and heart failure.
- Its effects on severe hemorrhagic shock are not well-studied.
Purpose of the Study:
- To investigate the impact of carvedilol on severe hemorrhagic shock in a rat model.
- To assess carvedilol's influence on mortality, hemodynamics, and inflammatory markers.
Main Methods:
- Male Sprague-Dawley rats received oral carvedilol (10 mg/kg/day) or no medication for 5 days.
- Severe hemorrhagic shock was induced via exsanguination, followed by blood reinfusion.
- Hemodynamics, arterial blood gases, mortality, and plasma cytokine levels (TNF-alpha) were measured.
Main Results:
- Carvedilol treatment significantly increased mortality rates (50% vs. 8% in controls) at 5 hours post-shock.
- Control rats showed less severe increases in base deficit and lactate levels.
- Tumor necrosis factor-alpha (TNF-alpha) levels were significantly lower in controls compared to the carvedilol group.
Conclusions:
- Oral carvedilol administration demonstrated adverse effects on survival and inflammatory responses in rats with severe hemorrhagic shock.
- These findings suggest carvedilol may negatively impact recovery from severe hemorrhagic shock.
Abstract:
The nonselective beta-adrenoceptor and the selective alpha1-adrenoceptor blocker carvedilol are widely used in hypertensive and/or cardiac failure patients because of its efficacy. However, there have been few studies regarding the effects of carvedilol on severe hemorrhagic shock. The present study was performed to evaluate the effects of carvedilol on severe hemorrhagic shock in rats. Twenty-four male Sprague-Dawley rats were randomly assigned to 1 of the following 2 groups (n = 12 per group): control group, no medication; and treatment group, oral administration of carvedilol (10 mg/kg per day) for 5 days. All animals were anesthetized with i.p. pentobarbital. Severe hemorrhagic shock was induced by partial exsanguination. Eight minutes after shock, all removed blood was returned to the animal. No other treatments were administered before, during, or after shock. Hemodynamics and arterial blood gases were recorded, mortality was calculated for the 5-h observation period, and plasma cytokine concentrations were measured at 5 h after shock. The mortality rates at 5 h after cardiac arrest were 8% and 50% for control and treatment groups, respectively. The increases in base deficit and lactate concentrations were less in the control group than that in the treatment group. Moreover, the increases in TNF-alpha concentrations were less in the control group than in the treatment group. The present study indicated that oral administration of carvedilol had adverse effects on mortality and inflammatory responses to severe hemorrhagic shock in rats. These findings suggest that carvedilol may adversely affect recovery from severe hemorrhagic shock.
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