Changes In Plasma Irisin And BDNF In Response To 7-day Cold-water Acclimation In Young Males

Cold water immersion can elicit strong physiological responses (i.e., shivering, hemodynamics), and has garnered interest for its potential therapeutic benefits when repeated via an acclimation. Irisin is a myokine that increases the expression of mitochondrial uncoupling and may affect metabolic activity during acute bouts of cold exposure. Further, irisin potentially plays a role in neural protection via stimulation of brain-derived neurotropic factor (BDNF), a circulating cytoprotective protein that also increases during acute cold exposure. While it is known that cold acclimation can alter thermoregulatory responses, such as shivering, it is unclear how acclimation may alter circulating cytoprotective proteins. PURPOSE: To evaluate the effect of 7-day cold-water acclimation on circulating irisin and BDNF concentrations during cold-water immersion throughout acclimation. METHODS: Six healthy, habitually active young males (23 ± 3 years) underwent a 7-day cold-water acclimation using 14 °C water for 60 min per day. Core temperature (esophageal) was measured continuously throughout each exposure. Plasma was collected intravenously before and after cold exposure on the first, fourth, and last day of acclimation. Lactate (a surrogate for changes in shivering), irisin, and BDNF were analyzed via enzyme-linked immunosorbent assays (ELISA), reported as changes from baseline values (means [SD]), and were analyzed via a one-way repeated measures ANOVA with Bonferroni correction (α = 0.05). RESULTS: No changes in BDNF were observed following cold exposure between any of the assessed days (p ≥ 0.397). Similarly, although core temperature significantly reduced with each day (-0.6 °C, p = 0.001), no changes between days were observed (p = 0.161). Irisin was significantly lower (p = 0.041) on day 7 (-367 pg/mL [400]) than day 1 (69 pg/mL [380]), but not day 4 (-132 pg/mL [425]). Similarly, lactate was significantly lower on day 7 (0.15 umol/mL [0.28]) compared to day 1 (0.36 umol/mL [0.24], p = 0.047), but not day 4 (28 umol/mL [0.29], p = 0.295). CONCLUSION: Given similar decreases in lactate (indicating reduced shivering) and irisin throughout the acclimation, irisin stimulation may only occur during the acute cold stress response associated with shivering, without influencing BDNF production. Supported by: National Sciences and Engineering Research Council of Canada

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Journal
Medicine & Science in Sports & Exercise
Published
2025-09-16
DOI
https://doi.org/10.1249/01.mss.0001160516.15313.8b
Primary Topic
Adipose Tissue and Metabolism
Type
article
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article

Changes In Plasma Irisin And BDNF In Response To 7-day Cold-water Acclimation In Young Males

Sindhu R. Johnson, Glen Patrick Kenny, Kelli E. King, James J. McCormick
Medicine & Science in Sports & Exercise
Adipose Tissue and Metabolism
article

Changes In Plasma Irisin And BDNF In Response To 7-day Cold-water Acclimation In Young Males

Sindhu R. Johnson, Glen Patrick Kenny, Kelli E. King, James J. McCormick
article en

Abstract

Cold water immersion can elicit strong physiological responses (i.e., shivering, hemodynamics), and has garnered interest for its potential therapeutic benefits when repeated via an acclimation. Irisin is a myokine that increases the expression of mitochondrial uncoupling and may affect metabolic activity during acute bouts of cold exposure. Further, irisin potentially plays a role in neural protection via stimulation of brain-derived neurotropic factor (BDNF), a circulating cytoprotective protein that also increases during acute cold exposure. While it is known that cold acclimation can alter thermoregulatory responses, such as shivering, it is unclear how acclimation may alter circulating cytoprotective proteins. PURPOSE: To evaluate the effect of 7-day cold-water acclimation on circulating irisin and BDNF concentrations during cold-water immersion throughout acclimation. METHODS: Six healthy, habitually active young males (23 ± 3 years) underwent a 7-day cold-water acclimation using 14 °C water for 60 min per day. Core temperature (esophageal) was measured continuously throughout each exposure. Plasma was collected intravenously before and after cold exposure on the first, fourth, and last day of acclimation. Lactate (a surrogate for changes in shivering), irisin, and BDNF were analyzed via enzyme-linked immunosorbent assays (ELISA), reported as changes from baseline values (means [SD]), and were analyzed via a one-way repeated measures ANOVA with Bonferroni correction (α = 0.05). RESULTS: No changes in BDNF were observed following cold exposure between any of the assessed days (p ≥ 0.397). Similarly, although core temperature significantly reduced with each day (-0.6 °C, p = 0.001), no changes between days were observed (p = 0.161). Irisin was significantly lower (p = 0.041) on day 7 (-367 pg/mL [400]) than day 1 (69 pg/mL [380]), but not day 4 (-132 pg/mL [425]). Similarly, lactate was significantly lower on day 7 (0.15 umol/mL [0.28]) compared to day 1 (0.36 umol/mL [0.24], p = 0.047), but not day 4 (28 umol/mL [0.29], p = 0.295). CONCLUSION: Given similar decreases in lactate (indicating reduced shivering) and irisin throughout the acclimation, irisin stimulation may only occur during the acute cold stress response associated with shivering, without influencing BDNF production. Supported by: National Sciences and Engineering Research Council of Canada

Medicine & Science in Sports & ExerciseVol. 57(10S)
University of Ottawa (CA)
Openalex Percentile: Top 69%
Adipose Tissue and Metabolism
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