Seasonal variations in cyclic AMP production by peripheral blood mononuclear cells in allergic asthmatics
Article first published online: 23 SEP 2008
Blackwell Science Ltd, Oxford
Clinical & Experimental Allergy
Volume 28, Issue 3, pages 271–277, March 1998
How to Cite
Hoekstra, Weersink, Postma and Kauffman (1998), Seasonal variations in cyclic AMP production by peripheral blood mononuclear cells in allergic asthmatics. Clinical & Experimental Allergy, 28: 271–277. doi: 10.1046/j.1365-2222.1998.00208.x
- Issue published online: 23 SEP 2008
- Article first published online: 23 SEP 2008
- cyclic AMP;
- allergic asthma;
- circannual variation;
Dysfunction of the β-adrenoceptor (βAR)/adenylyl cyclase (AC) system can impair the response of different cell types, including lymphocytes. In asthma, impairment of this system as well as changes in cytokine production by lymphocytes have been described. Because the severity of asthma can change over the year, a circannual pattern of the βAR/AC system activity may also exist.
We set out to examine the activity of this βAR/AC signal transduction system in peripheral blood mononuclear cells (PBMCs) of allergic asthmatics to asses whether differences existed between seasons. We investigated whether changes were associated with asthma severity and circannual changes in serum cortisol levels.
During 19 months, 41 allergic asthmatics (mean age 28 years) with nocturnal airway obstruction were enrolled in the study. AC activity was measured by cyclic AMP production. Resting, stimulated and potentiated AC activities and their relationships with clinical parameters, seasonal influences and serum cortisol levels were assessed.
The AC activity in resting, stimulated and potentiated cells varied during the year. AC activity was relatively low in the periods June–August and September–November, and higher in December–February and March–May. Receptor-mediated and potentiated responses expressed as percentage of the resting response were equivalent throughout the year. Serum cortisol levels were positively related to AC activity. No relationships were found between clinical parameters and AC activity or serum cortisol levels.
These results indicate that AC activity in PBMCs of allergic asthmatics shows a seasonal variation. However, seasonal differences in AC activity seems to be unrelated with clinical parameters. Other factors such as serum cortisol levels may have a modulating influence on AC activity. Future studies of AC systems in blood cells of asthmatic patients need to take into account these seasonal influences.