Newswise — March 31, 2022  – Resistance or strength training protects against the development of muscle pain in mice – and does so by activating androgen receptors, reports a basic science study in PAIN®, the official publication of the International Association for the Study of Pain (IASP). The journal is published in the Lippincott portfolio by Wolters Kluwer.

The study supports the role of testosterone and male sex hormone (androgen) receptors in preventing or relieving muscle pain in response to resistance training, according to the report by Kathleen A. Sluka, PT, PhD, FAPTA, and colleagues of The University of Iowa, Iowa City. "This information provides a scientific basis for the use of strength training as a therapeutic tool clinically for individuals with chronic musculoskeletal pain," the researchers write.

Testosterone mediates benefits of exercise on muscle pain

Exercise is commonly prescribed for patients with many types of chronic pain, such as low back pain, osteoarthritis, and fibromyalgia. Although many studies have examined the analgesic effects of exercise, less is known about how resistance training affects musculoskeletal pain. Previous studies by the same research group found that testosterone protects against the development of increased pain (hyperalgesia).

Graduate student Joseph Lesnak, PT, designed a new model to assess the effects of resistance training on muscle pain in mice. Strength training is a commonly used treatment by physical therapy clinicians for management of pain. In the experimental setup, mice climbed a ladder with small weights gently attached to their tails.

Tests confirmed that ladder-climbing was an effective form of resistance training, resulting in increased strength of the front paws. Activity-induced muscle pain was induced in some groups of mice by injection of a mild acid solution. The goal was to evaluate how resistance training affected the development of musculoskeletal pain, including the effects of testosterone levels and androgen receptors.

"Eight weeks of resistance training prior to induction of the pain model blocked the development of muscle pain in both male and female mice," Dr. Sluka and coauthors write. However, once muscle pain was established, the ladder-climbing exercise alleviated pain only in male mice. Exercise also led to short-term increases in testosterone in male mice, but not females.

To confirm the effects of testosterone on muscle pain, the researchers performed further experiments using an androgen receptor- blocking drug. Animals that received the androgen blocker during resistance training did not develop the protective effect against muscle pain. Once the exercise-induced protective effect was present, it was unaffected by the androgen blocker.

"These data suggest that activation of androgen receptors is required for the protection against activity-induced muscle pain that is produced by the resistance training program," the researchers write.  The findings in their animal model may provide useful insights into the use of exercise as a treatment for chronic pain.

"Since both aerobic and resistance training-based exercise produce analgesia, clinicians may want to consider patient preferences when prescribing exercise modes," Dr. Sluka and colleagues write. The analgesic effect appears to be systemic, suggesting that strength training does not need to be targeted at the painful muscles for therapeutic benefits.

The results also suggest that resistance training will be more effective in preventing muscle pain, rather than alleviating it. "This suggests that exercise should be continued in the absence of symptoms to prevent against future development of musculoskeletal pain," the researchers conclude.

Click here to read “Resistance training protects against muscle pain through activation of androgen receptors in male and female mice”

DOI: 10.1097/j.pain.0000000000002638

###

About PAIN

PAIN is IASP's official journal. Published monthly, PAIN presents original research on the nature, mechanisms, and treatment of pain. Available to IASP members as a membership benefit, this peer-reviewed journal provides a forum for the dissemination of multidisciplinary research in the basic and clinical sciences. It is cited in Current Contents and Index Medicus.

About the International Association for the Study of Pain

IASP is the leading professional organization for science, practice, and education in the field of pain. Membership is open to all professionals involved in research, diagnosis, or treatment of pain. IASP has more than 7,000 members in 133 countries, 90 national chapters, and 20 special interest groups (SIGs). IASP brings together scientists, clinicians, health-care providers, and policymakers to stimulate and support the study of pain and translate that knowledge into improved pain relief worldwide.

About Wolters Kluwer

Wolters Kluwer (WKL) is a global leader in professional information, software solutions, and services for the clinicians, nurses, accountants, lawyers, and tax, finance, audit, risk, compliance, and regulatory sectors. We help our customers make critical decisions every day by providing expert solutions that combine deep domain knowledge with advanced technology and services.

Wolters Kluwer reported 2020 annual revenues of €4.6 billion. The group serves customers in over 180 countries, maintains operations in over 40 countries, and employs approximately 19,200 people worldwide. The company is headquartered in Alphen aan den Rijn, the Netherlands.

Wolters Kluwer provides trusted clinical technology and evidence-based solutions that engage clinicians, patients, researchers and students in effective decision-making and outcomes across healthcare. We support clinical effectiveness, learning and research, clinical surveillance and compliance, as well as data solutions. For more information about our solutions, visit https://www.wolterskluwer.com/en/health and follow us on LinkedIn and Twitter @WKHealth.

For more information, visit www.wolterskluwer.com, follow us on TwitterFacebookLinkedIn, and YouTube.

Journal Link: PAIN®