Antihistamines
Histamine is a biogenic amine derived from histidine that acts as a mediator of inflammation and anaphylactic reactions, a mediator in the CNS and is also involved in the regulation of gastric secretion. Antihistamines (H1-, H2- and H3-lytics) are drugs that specifically block the effects of histamine on histaminergic receptors.
H1-lytics[edit | edit source]
H1-lytics are competitive antagonists at H1 receptors. They inhibit the vascular response to histamine, including increased permeability (edema formation), but do not affect the symptoms of shock. Although they are potent inhibitors of bronchoconstriction in vitro, they are not able to sufficiently influence the mechanisms of asthma.
Indication[edit | edit source]
- symptomatic treatment of allergic diseases: allergic rhinitis (eg hay fever); urticaria, Quincke's edema, drug and food allergy;
- pruritus of various origins with the exception of pruritus for cholestasis (eg allergic and non-allergic pruritic dermatoses, pruritus for infectious diseases accompanied by rash, such as chickenpox, measles, rubella);
- insect bites (locally, eg Template: HVLP - Fenistil®);
- kinetosis (balance disorders due to processes on the inner ear) - vertigo, morbid Meniér;
- nausea and vomiting of various etiologies (except organic disorders of the GIT);
- insomnia (CNS inhibition).
Pharmacokinetics[edit | edit source]
Conventional H1-lytics - 1st generation - for a short half-life must be administered several times a day. They penetrate the CNS, which manifests itself as sedentary. Generation 2 substances have a longer duration of action (can be administered once daily - Template: HVLP) and do not penetrate the CNS (they are not sedative).
Side effects[edit | edit source]
- The sedative effect, attenuation of psychomotor activity, is noticeable, especially in older drugs. Attention should be drawn to the reduced ability to drive and participate in traffic as well as to operate demanding machinery.
- Antimuscarinic effects (dry mouth, blurred vision, urinary retention in prostate hyperplasia, etc.).
- QT prolongation by a direct effect on the myocardium. By this mechanism, the electrical instability of the myocardium can be amplified with the consequent induction of torsade de pointes tachyarrhythmias.
| Active substance | Effect time (hours) | Sedative effect | Single dose for adults (mg) |
|---|---|---|---|
| promethazine | 20 | +++ | 10–20 |
| cyproheptadine | 5 | + | 4 |
| bisulepine | 7 | + | 2 |
| dimetinden | 7 | + | 1–2 |
| moxastine | 2 | +++ | 25–100 |
2nd generation H1-lytics are substances with minimal sedative effects and prolonged H1 lytic effects.
| Active substance | Effect time (hours) | Sedative effect | Single dose for adults (mg) |
|---|---|---|---|
| cetirizine | 24 | 0 | 10 |
| loratadine | 24 | 0 | 10 |
Links[edit | edit source]
Related articles[edit | edit source]
Literature[edit | edit source]
- MARTÍNKOVÁ, Jiřina, Stanislav MIČUDA a Jolana ČERMÁKOVÁ. Vybrané kapitoly z klinické farmakologie pro bakalářské studium : Histamin, antihistaminika [online]. ©2001. [cit. 2010-07-13]. <https://www.lfhk.cuni.cz/farmakol/predn/bak/kapitoly/histamin-bak.doc/>.
