Origin and Chemical Properties
Quinine is a natural alkaloid extracted from the cinchona bark. Historically, it is the oldest antimalarial agent, utilized in European medical practice since 1632.
Chemically, a close relative of the drug is quinidine. It acts as an optical isomer of quinine and exhibits a nearly identical spectrum of pharmacological properties.
Mechanism of Action
The antimalarial effect of the substance is achieved through several pathways:
- Disruption of normal heme metabolism within the parasite.
- Direct insertion (intercalation) into the Plasmodium DNA molecule via hydrogen bond formation.
- Prevention of nucleic acid strand separation, leading to the inhibition of transcription and translation processes.
Clinical Use in Malaria
The drug has strict indications and limitations in modern therapy:
- It is used exclusively for treatment of the disease.
- It is employed only against the erythrocytic stage of malaria.
- It is absolutely not used for disease prophylaxis.
Side Effects and Toxicity
The toxic effects of the compound manifest with specific symptoms:
- Cinchonism: a complex of pathological signs including severe tinnitus, temporary deafness, pronounced headache, nausea, vomiting, and various visual disturbances.
- Cardiotoxicity: the ability to provoke dangerous arrhythmias and cause QT interval prolongation on the electrocardiogram.