Tabata Exercise on Nitric Oxide Synthases and Maresin

February 9, 2026 updated by: Zafer Bayraktutan, Ataturk University

Differential Effects of Tabata Exercise on Nitric Oxide Synthases and Maresin in Smokers and Non-Smokers

Smoking causes chronic inflammation and endothelial dysfunction through alterations in nitric oxide synthase (NOS) pathways. Maresin is an anti-inflammatory pro-resolving lipid mediator that plays important roles in the resolution of inflammatory processes. Tabata exercise is a short-duration, high-intensity exercise modality with beneficial effects on the cardiovascular system. The aim of this study was to comparatively evaluate the effects of tabata exercise on iNOS, eNOS, and Maresin levels, as well as the relationships among these biomarkers, in smokers and non-smokers.

Study Overview

Status

Completed

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Age between 18 and 40 years
  • No regular participation in structured physical exercise for at least 6 months prior to enrollment
  • Absence of any acute or chronic inflammatory disease at baseline
  • No history of cardiovascular, metabolic, pulmonary, or neurological disorders
  • Ability to comply with the study protocol and complete the tabata exercise program
  • Provision of written informed consent

Exclusion Criteria:

  • Initiation or cessation of smoking during the study period
  • Use of anti-inflammatory, antioxidant, corticosteroid, or vasoactive medications
  • Acute infection, surgical intervention, or major trauma within the preceding 3 months
  • Diagnosis of diabetes mellitus, hypertension, coronary artery disease, or chronic pulmonary disease
  • History of alcohol or substance abuse
  • Pregnancy or breastfeeding
  • Musculoskeletal or orthopedic conditions that could limit participation in tabata exercise
  • Inability to adhere to the exercise protocol or failure to complete follow-up assessments

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Smoker
  • Current smokers with a smoking history of at least 2 years
  • Daily cigarette consumption of ≥10 cigarettes per day

The Tabata protocol consisted of 20-second high-intensity intervals exceeding 70 % of VO₂max and approaching ~90 % of VO₂max, followed by 10 seconds of rest, repeated for 4 minutes per set. Exercises included high knees, froggers, speed skaters, jumping jacks, and mountain climbers. Following the original Tabata design [29], each work-rest cycle was repeated eight times.

Each training session began with a 10-15 minute warm-up and concluded with a 10-15 minute cool-down. The total number of sets ranged from 1 to 4, and the number of exercises per session ranged from 4 to 8. Training intensity progressively increased from 30 % to 89 % of maximal effort according to the principle of progressive overload.

Active Comparator: Nonsmoker
  • Individuals who had never smoked, or
  • Individuals who had not smoked for at least 5 years, with no history of regular passive smoking exposure

The Tabata protocol consisted of 20-second high-intensity intervals exceeding 70 % of VO₂max and approaching ~90 % of VO₂max, followed by 10 seconds of rest, repeated for 4 minutes per set. Exercises included high knees, froggers, speed skaters, jumping jacks, and mountain climbers. Following the original Tabata design [29], each work-rest cycle was repeated eight times.

Each training session began with a 10-15 minute warm-up and concluded with a 10-15 minute cool-down. The total number of sets ranged from 1 to 4, and the number of exercises per session ranged from 4 to 8. Training intensity progressively increased from 30 % to 89 % of maximal effort according to the principle of progressive overload.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
serum inducible nitric oxide synthase (iNOS) level
Time Frame: 6 week after exercise
iNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
6 week after exercise
serum inducible nitric oxide synthase (iNOS) level
Time Frame: 12 week after exercise
iNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
12 week after exercise
serum endothelial nitric oxide (eNOS) synthase level
Time Frame: 6 week after exercise
eNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
6 week after exercise
serum endothelial nitric oxide (eNOS) synthase level
Time Frame: 12 week after exercise
eNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
12 week after exercise

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
serum maresin level
Time Frame: 6 week after exercise
Maresin level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
6 week after exercise
serum maresin level
Time Frame: 12 week after exercise
Maresin level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
12 week after exercise

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 24, 2025

Primary Completion (Actual)

January 16, 2026

Study Completion (Actual)

January 30, 2026

Study Registration Dates

First Submitted

February 9, 2026

First Submitted That Met QC Criteria

February 9, 2026

First Posted (Actual)

February 17, 2026

Study Record Updates

Last Update Posted (Actual)

February 17, 2026

Last Update Submitted That Met QC Criteria

February 9, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • ATAUNISPORT1

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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