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Physiological Effect of Ataulfo Mango (Manguifera Indica) Beverage in Exercise

Not Applicable
Completed
Conditions
Exercise-induced Oxidative Stress
Interventions
Dietary Supplement: Mango pulp beverage
Dietary Supplement: Mango pulp and peel beverage
Dietary Supplement: Control beverage
Registration Number
NCT03182543
Lead Sponsor
Universidad Autonoma de Ciudad Juarez
Brief Summary

The aim of this study is to assess the antioxidant capacity of two mango base beverages (AM1, AM2), against exercise-induced oxidative stress.

Detailed Description

Introduction. The post-consumption physiological effect of mango cv. "Ataulfo" pulp (MP) and peel (MC) in humans before exercise has been poorly evaluated.

Objective. To evaluate the physiological response, to consumption of two mango base beverages, AM1 (200g MP/ 600mL water) and AM2 (160g MP; 40g MC / 600mL water), before and after a submaximal exercise test.

Methods. The antioxidant profile and physicochemical characteristics of AM1 and AM2 were evaluated. Several cardiorespiratory, anthropometric and body composition parameters of 19 university students, prior to the consumption of AM1, AM2 and water, were evaluated in three non-consecutive sessions (self-control cases). The glycemic, lactic and antioxidant (FRAP), uric acid (AU), reduced glutathione (GSH) and lipid oxidation (TBARS) and protein carbonyls (PC) responses were evaluated in plasma before and after an incremental cycle ergometer exercise test.

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
19
Inclusion Criteria
  • healthy male
  • university student
  • no alcohol, cigar or drugs consumption
Exclusion Criteria
  • no antioxidant supplement or ergogenic consumption
  • health issues with performing physical activity

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
AM1Mango pulp beverageMango pulp beverage
AM2Mango pulp and peel beverageMango pulp and peel beverage
ControlControl beverageControl beverage
Primary Outcome Measures
NameTimeMethod
Antioxidant capacity change0 min (before beverage intake), 9-15 (immediately after exercise test)

Assessed by reduced glutathione concentration change. Blood samples were drawn from the antecubital vein into EDTA test tubes at rest, before beverage intake, and immediately following the exercise test. Samples were then centrifuged at 5000 rpm for 10 min at 4°C to obtain plasma, which was withdrawn and separated into eppendorf vials, maintained at -80°C until further biochemical analysis.

Secondary Outcome Measures
NameTimeMethod
Oxidative stress change0 min (before beverage intake), 9-15 (immediately after exercise test)

Assessed by protein carbonyls concentration change. Blood samples were drawn from the antecubital vein into EDTA test tubes at rest, before beverage intake, and immediately following the exercise test. Samples were then centrifuged at 5000 rpm for 10 min at 4°C to obtain plasma, which was withdrawn and separated into eppendorf vials, maintained at -80°C until further biochemical analysis.

Lactic acid concentration change0 min (before performing exercise test), 3 min, 6 min, 9 min, 12 min, 15 min (during exercise test)

Assessed by lactic acid concentration change. Capillary blood samples were taken from the fingertip, using a lancet and analyzed (YSI modelo 1500, Yellow Springs, USA)

Postprandial glycemic change0 min (before beverage intake), 30 min, 60 min, 90 min, 120 min (after beverage intake)

Assessed by blood glucose concentration change. Capillary blood samples were taken from the fingertip, using a lancet, and analyzed (ReliOn Confirm/micro Test Strips ARKRAY, USA)

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