Anesthetic Agents Isoflurane and Propofol Decrease Maximal Ca2+-Activated Force and Thus Contractility in the Failing
Tao Meng1, Xianfeng Ren1, Xinzhong Chen1
1Department of Anesthesiology, Qilu Hospital of Shandong University, Jinan, Shangdong, China (T.M., J.Y.); Department of Anesthesiology, China-Japan Friendship Hospital, Beijing, China (X.R.); Department of Cardiac Surgery, Tongji University Medical Center, Wuhan, China (X.C.); Division of Cardiology (J.A., N.P.) and Department of Anesthesiology and Critical Care Medicine (W.D.G.), Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; and Department of Biomedical Sciences, University of Padova, Padova, Italy (N.P.).
Abstract:
In the normal heart, frequently used anesthetics such as isoflurane and propofol can reduce inotropy. However, the impact of these agents on the failing myocardium is unclear. Here, we examined whether and how isoflurane and propofol influence cardiac contractility in intact cardiac muscles from rats treated with monocrotaline to induce heart failure. We measured force and intracellular Ca2+ ([Ca2 +]i) in trabeculae from the right ventricles of the rats in the absence or presence of propofol or isoflurane. At low to moderate concentrations, both propofol and isoflurane dose-dependently depressed cardiac force generation in failing trabeculae without altering [Ca2+]i At high doses, propofol (but not isoflurane) also decreased amplitude of [Ca2+]i transients. During steady-state activation, both propofol and isoflurane impaired maximal Ca2+-activated force (Fmax) while increasing the amount of [Ca2+]i required for 50% of maximal activation (Ca50). These events occurred without apparent change in the Hill coefficient, suggesting no impairment of cooperativity. Exposing these same muscles to the anesthetics after fiber skinning resulted in a similar decrement in Fmax and rise in Ca50 but no change in the myofibrillar ATPase-Ca2+ relationship. Thus, our study demonstrates that challenging the failing myocardium with commonly used anesthetic agents such as propofol and isoflurane leads to reduced force development as a result of lowered myofilament responsiveness to Ca2+ SIGNIFICANCE STATEMENT: Commonly used anesthetics such as isoflurane and propofol can impair myocardial contractility in subjects with heart failure by lowering myofilament responsiveness to Ca2+. High doses of propofol can also reduce the overall amplitude of the intracellular Ca2+ transient. These findings may have important implications for the safety and quality of intra- and perioperative care of patients with heart failure and other cardiac disorders.
Insights
Common anesthetics like isoflurane and propofol reduce heart muscle contractility in heart failure by decreasing myofilament responsiveness to calcium (Ca2+). High propofol doses also lower Ca2+ transient amplitude.
Area of Science:
- Cardiology
- Anesthesiology
- Physiology
Background:
- Anesthetics like isoflurane and propofol affect cardiac contractility.
- Their impact on failing myocardium remains unclear.
- Heart failure is a significant clinical concern.
Purpose of the Study:
- To investigate the effects of isoflurane and propofol on cardiac contractility in heart failure.
- To elucidate the underlying mechanisms of anesthetic-induced contractility changes.
Main Methods:
- Used rat models of monocrotaline-induced heart failure.
- Measured force and intracellular calcium ([Ca2+]i) in isolated cardiac trabeculae.
- Administered varying concentrations of isoflurane and propofol.
- Performed fiber-skinning experiments to assess myofilament function.
Main Results:
- Both anesthetics dose-dependently reduced force in failing hearts without altering [Ca2+]i at low/moderate doses.
- High-dose propofol decreased [Ca2+]i transient amplitude.
- Isoflurane and propofol impaired maximal Ca2+-activated force (Fmax) and increased Ca50, indicating reduced myofilament responsiveness to Ca2+.
- No changes in cooperativity or myofibrillar ATPase-Ca2+ relationship were observed.
Conclusions:
- Isoflurane and propofol impair contractility in failing myocardium by reducing myofilament Ca2+ responsiveness.
- Propofol may also affect Ca2+ transient amplitude at high doses.
- Findings have implications for anesthetic management in heart failure patients.
Related Concept Videos
Local Anesthetics: Common Agents and Their Applications
Cocaine is an ester of benzoic acid and methylecgogine. It is used to anesthetize and vasoconstrict locally. Currently, it is used primarily for topical applications. It is beneficial for surgeries on the upper respiratory tract, providing anesthesia and shrinking the mucosa. Cocaine in the form of cocaine hydrochloride is...
14:52Recording Brain Electromagnetic Activity During the Administration of the Gaseous Anesthetic Agents Xenon and Nitrous Oxide in Healthy Volunteers
09:49Procedures for Rat in situ Skeletal Muscle Contractile Properties
09:50Application of Chronic Stimulation to Study Contractile Activity-induced Rat Skeletal Muscle Phenotypic Adaptations
07:03Intrauterine Telemetry to Measure Mouse Contractile Pressure In Vivo
14:02Ex Vivo Assessment of Contractility, Fatigability and Alternans in Isolated Skeletal Muscles
We describe a method to directly measure muscle force, muscle power, contractile kinetics and fatigability of isolated skeletal muscles in an in vitro system using field stimulation. Valuable information on Ca2+ handling properties and contractile machinery of the muscle can be obtained using different stimulating protocols.


