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Some methods for evaluating clinical itch and their application for studying pathophysiological mechanisms
1Department of Dermatology, Karolinska Hospital, Stockholm, Sweden.
Journal of Dermatological Science
|September 1, 1992
Summary
Quantitative measurements of clinical itch using a novel microcomputer system revealed that antihistamines do not treat atopic dermatitis itch. Cyclosporin A, a cytokine inhibitor, effectively reduced itch, suggesting cytokines, not histamine, are key itch triggers.
Area of Science:
- Dermatology
- Clinical pharmacology
- Neuroscience
Background:
- Measuring itch sensation in clinical research has been challenging.
- Atopic dermatitis is a common skin condition characterized by intense itching.
- The role of histamine and cytokines in mediating itch in atopic dermatitis is not fully understood.
Purpose of the Study:
- To introduce a microcomputer-based system for quantitative measurement of clinical itch.
- To evaluate the antipruritic effects of antihistamines and cyclosporin A in atopic dermatitis.
- To investigate the role of histamine and cytokines in the pathophysiology of itch in atopic dermatitis.
Main Methods:
- Development and utilization of a patient-operated, microcomputer-based system for symptom recording.
- Portable data loggers were used by patients to quantify their itch symptoms.
- Assessment of drug efficacy by measuring changes in self-reported itch intensity.
Main Results:
- The microcomputer system enabled quantitative measurements of clinical itch.
- Antihistamines did not show significant antipruritic effects in patients with atopic dermatitis.
- Cyclosporin A, a drug that inhibits cytokine production, effectively reduced itch in atopic dermatitis.
Conclusions:
- Histamine is likely not a major pruritogen (itch-inducing substance) in atopic dermatitis.
- Cytokines are implicated as key mediators of itch in atopic dermatitis.
- The developed microcomputer system is a valuable tool for assessing antipruritic drug effects.