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A Role for Cyclooxygenase and Nitric Oxide Synthase in Sweating and Skin Blood Flow During Exercise in the Heat in Young Individuals with Type 1 Diabetes
Author(s) -
Foudilbey Imane,
Fujii Naoto,
Dervis Sheila,
Kenny Glen P.
Publication year - 2016
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.30.1_supplement.1288.14
Subject(s) - microdialysis , sweat , nitric oxide synthase , nitric oxide , endocrinology , medicine , cyclooxygenase , vasodilation , chemistry , heart rate , type 2 diabetes , blood pressure , diabetes mellitus , biochemistry , enzyme , central nervous system
Recent studies show that individuals with type 1 diabetes mellitus (T1DM) have impaired heat loss responses. This is evidenced as a decrease in local sweat rate and an increase in core body temperature during exercise in the heat compared to non‐diabetic matches; however, the underlying mechanisms are currently unknown. Previous studies have shown that nitric oxide synthase (NOS) and cyclooxygenase (COX) increase sweating, while NOS, but not COX, contributes to cutaneous vasodilation in young adults exercising in the heat. Thus, the aim of our study was to determine if the impairments in local heat loss responses displayed by individuals with T1DM may be attributed to COX and/or NOS activity. Seven (5 males, 2 females) young (24±3 years) individuals with T1DM were instrumented with four microdialysis fibres in the forearm skin which were perfused with either 1) 10 mM ketorolac (KETO, non‐selective COX inhibitor), 2) 10 mM N G ‐nitro‐ L ‐arginine methyl ester (L‐NAME, non‐selective NOS inhibitor), 3) a combination of L‐NAME and KETO (L‐NAME+KETO), or 4) lactated Ringer (Control). Sweat rate (ventilated capsule) and cutaneous vascular conductance (CVC; laser Doppler perfusion units/mean arterial pressure) were measured continuously throughout the protocol. Participants performed two 30 min bouts of exercise at a fixed rate of heat production of 400 W in the heat (35°C, 20% relative humidity); separated by a 20‐ and 40‐min recovery respectively. During the first and second exercise bouts, we showed that the inhibition of COX (KETO) resulted in an increase in sweat rate relative to Control (average of last 5 min of second exercise; Control: 1.02±0.11 mg min −1 cm −2 , KETO: 1.12±0.12 mg min −1 cm −2 ; P=0.029). However, a decrease in sweat rate was observed when both NOS and COX were inhibited (L‐NAME+KETO: 0.86±0.11 mg min −1 cm −2 ; P=0.031). Furthermore, inhibition of NOS alone did not significantly modulate sweating (L‐NAME: 0.93±0.11 mg min −1 cm −2 ; P=0.11). With respect to CVC, the inhibition of NOS (average of last 5 min of second exercise, 45±9%max), as well as NOS and COX (49±4%max) resulted in similar decreases in CVC relative to Control (68±1%max)(both P<0.05). In contrast, the inhibition of COX alone did not modulate CVC (64±4%max; P=0.33). Our results demonstrate that COX attenuates sweating during exercise in the heat in young adults with T1DM, which may occur through NOS‐dependent mechanisms. Finally, we show that individuals with T1DM exhibit NOS‐ but not COX‐dependent cutaneous vasodilation during exercise in the heat. Support or Funding Information This study was supported by grants from the Canadian Institutes of Health Research (286363; funds held by Dr. Glen P. Kenny).