Mechanism of action[edit | edit source]
A common feature for all groups is the presence of a β-lactam ring, which damages the cell walls of bacteria, resulting in the death of the microorganism. They prevent the formation of a three-dimensional structure of bacterial cell walls. This occurs through three mechanisms:
- binding to penicillin-binding proteins (penicillin-binding proteins, PBP);
- inhibition of cell wall synthesis by interrupting peptidoglycan transpeptidation u (peptidoglycan is a polymer that imparts shape and stiffness to bacteria);
- activation of enzymes that act lytically on the cell wall.
In therapeutic findings, the effect is bactericidal. For penicillins and cephalosporins, bactericide is restricted to cells with active peptidoglycan synthesis (ie, proliferating, in the growth phase). The different efficacy in G+ and G− bacteria lies in the combination of different types of PBP proteins, the number of inactivating enzymes, the number of binding sites and the affinity for PBP.
Pharmacokinetics and pharmacodynamics[edit | edit source]
Absorption from the GIT depends on resistance to HCl. It can be reduced by eating at the same time, so take it at least 1 hour before a suitable meal. β-tamas are hydrophilic substances that do not penetrate intracellularly, they remain in the extracellular space, where they mimic plasma concentration. Concentrations in the CNS are low, we are looking for inflammatory meningeal changes. They are excreted by the kidneys, sold in milk and sputum.
It has a time-dependent effect, suggesting that high concentrations have an effect similar to those just above the MIC. For maximum effect, the concentration level should be kept above the MIC as long as possible.
Resistance[edit | edit source]
Enzymatic resistance[edit | edit source]
It rests in the bacterial production of inactivating enzymes (beta-lactamases), which cleave the β-lactam ring.
Non-enzymatic resistance[edit | edit source]
A change in the structure of PBP, that causes an antibiotic not to recognize its receptor site and decreases its affinity for the receptor. The change can occur either by modifying the binding site or by creating new PBP variants. We often encounter this type at MRSA.
Another possibility of developing resistance is the impermeability of the outer membrane (by reducing the number of porins). Antibiotics do not reach receptor sites. This type can be found exclusively in nosocomial multidrug-resistant G− microorganisms.
Resistance also occurs through the formation of efflux pumps, which are responsible for the active elimination of xenobiotics from cells.
The development of secondary resistance is possible but slow.
Links[edit | edit source]
Related articles[edit | edit source]
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References[edit | edit source]
- MARTÍNKOVÁ, Jiřina – MIČUDA, Stanislav – CERMANOVÁ, Jolana. Vybrané kapitoly z klinické farmakologie pro bakalářské studium [online]. [cit. 2010-05-23]. <https://www.lfhk.cuni.cz/farmakol/predn/prednbak.htm/>.
Bibliography[edit | edit source]
- MARTÍNKOVÁ, Jiřina, et al. Farmakologie pro studenty zdravotnických oborů. 2. edition. Praha : Grada, 2018. ISBN 978-80-271-0929-6.
- ŠVIHOVEC, Jan, et al. Farmakologie. 1. edition. Praha : Grada, 2018. ISBN 978-80-271-2150-2.