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Updated: May 11, 2025

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
Published on: July 29, 2014
Effects of intravenous morphine and lidocaine on bacterial growth
Cristiana Iulia Osoian1,2, Stanca Lucia Pandrea3,4, Mirela Flonta5
11st Department of Anesthesia and Intensive Care, Iuliu Hatieganu University of Medicine and Pharmacy, 8 Victor Babes Street, Cluj-Napoca, CJ, 400012, Romania.
Background:
Infection prevention and control remain critical challenges in the ICU. Morphine, a frequently used opioid for postoperative pain management, may indirectly promote infections, whereas lidocaine might have protective effects. However, data regarding the direct influence of morphine and lidocaine, at concentrations within the range of plasma concentrations, on common ICU bacterial strains are lacking. This is the first study to investigate the direct effects of morphine and lidocaine at plasma concentrations corresponding to possible clinical settings, as seen in multimodal analgesia regimens, on bacterial growth using microbiological assays and transmission electron microscopy.
Methods:
Morphine (1000 ng/ml, 2000 ng/ml) and lidocaine (4 µg/ml, 10 µg/ml) were placed in contact with standard strains of Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus and tested using diffusion method, broth dilution method, and time-kill assay. Additionally, E. coli, P. aeruginosa and S. aureus were exposed to lidocaine 10 µg/ml and examined via transmission electron microscopy.
Results:
Morphine and lidocaine exhibited neither stimulatory nor inhibitory effects on bacterial growth, regardless of concentration, volume, or exposure time in microbiological testing. In contrast, transmission electron microscopy revealed that lidocaine exposure altered bacterial ultrastructure, causing significant cell wall disorganization and rupture, alterations in cytoplasmic and nucleolar structure, and the appearance of "ghost cells", indicative of cell lysis.
Conclusions:
At plasma concentrations, morphine and lidocaine do not directly affect bacterial growth in vitro microbiological laboratory testing. Lidocaine on the other hand, in higher plasma concentrations, disrupts bacterial ultrastructure. Further studies are needed to investigate the significance and clinical impact of these findings.
Insights
Morphine and lidocaine do not directly impact bacterial growth at clinical plasma concentrations. However, higher lidocaine concentrations disrupt bacterial cell structure, suggesting potential antimicrobial effects warranting further investigation.
Area of Science:
- Microbiology
- Pharmacology
- Infection Control
Background:
- Infection prevention and control are critical in intensive care units (ICUs).
- Morphine (opioid) may indirectly promote infections, while lidocaine (local anesthetic) might offer protective effects.
- Limited data exist on the direct impact of morphine and lidocaine on common ICU bacteria at clinically relevant plasma concentrations.
Purpose of the Study:
- To investigate the direct effects of morphine and lidocaine on bacterial growth.
- To assess these effects at plasma concentrations relevant to multimodal analgesia.
- To utilize microbiological assays and transmission electron microscopy for analysis.
Main Methods:
- Standard bacterial strains (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus) were exposed to morphine and lidocaine at specified concentrations.
- Microbiological testing included diffusion, broth dilution, and time-kill assays.
- Transmission electron microscopy examined bacterial ultrastructure after lidocaine exposure.
Main Results:
- Morphine and lidocaine showed no stimulatory or inhibitory effects on bacterial growth in microbiological tests.
- Transmission electron microscopy revealed lidocaine disrupted bacterial cell walls, altered internal structures, and caused cell lysis ('ghost cells').
Conclusions:
- At plasma concentrations, morphine and lidocaine do not directly influence bacterial growth in vitro.
- Lidocaine, at higher concentrations, demonstrably disrupts bacterial ultrastructure.
- Further research is necessary to determine the clinical significance of these ultrastructural findings.
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