Over-the-Counter Antihistamines & Heat Stress
Allergic Rhinitis | Heat Illness | Sudomotor Sympathetic Dysfunction | Heat InjuryAllergic rhinitis (AR) currently affects \~25% of Canadians, and due to factors of climate change, this number is expected to increase over the coming decade. AR symptoms can significantly impact individuals' quality of life by compromising sleep, productivity, and social interactions. To alleviate AR symptoms, North Americans tend to rely on H1 antihistamine medications available over-the-counter (OTC) at most pharmacies. However, public health authorities currently suggest restraining all antihistamines during heat waves due to beliefs that M3 muscarinic receptor and H1 receptor antagonism, independent pharmacological mechanisms of H1 antihistamines, might suppress thermoregulatory responses to heat stress and increase individuals' susceptibility to heat-related illness/injury. To date, studies using supramaximal doses of antihistamines have demonstrated reductions in sweating, however these doses and administration routes are not the typical use case. Additional studies utilizing fexofenadine, a second-generation H1 antihistamine, have linked H1 receptor antagonism to reductions in skin blood flow, potentially impacting thermoregulation by reducing peripheral blood redistribution. Empirical evidence supporting OTC H1 antihistamines impacting thermoregulatory control at recommended doses is scarce. Thus, this study aims to systematically assess whether three common OTC H1 antihistamines, taken as prescribed, alter thermoregulatory responses during thermal stress.
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Participation Requirements
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Sex:
ALL -
Eligible Ages:
19 to 39
Participation Criteria
Inclusion Criteria:
* Male or Female between ages 19 and 39 years
* Fully vaccinated against COVID-19
* Able to provide informed consent
* Body-mass index under 30
Exclusion Criteria:
* Body-mass index over 30
* Currently taking sedative or autonomic nervous system depressant medication
* Hypersensitivity to diphenhydramine, loratadine, or desloratadine
* History of cardiovascular disease, cancer, type 1 or 2 diabetes, chronic obstructive pulmonary disorder, or cystic fibrosis
* Have smoked tobacco products less than 12 months prior to participation
* Pregnant/Breastfeeding
Study Location
Lakehead University C.J Sanders Fieldhouse
Lakehead University C.J Sanders FieldhouseThunder Bay, Ontario
Canada
Contact Study Team
- Study Sponsored By
- Lakehead University
- Participants Required
- More Information
- Study ID:
NCT06217367