Why Muscle Is More Than Just Strength: The Endocrine Powerhouse Hiding in Plain Sight

Challenging the Assumption: Muscle Is Just for Movement

When most people think about muscle, they think about strength, athleticism, and aesthetics. But this common understanding overlooks one of the most important roles of skeletal muscle: its function as a powerful endocrine organ. At Movability, we often see patients with fatigue, hormone imbalances, chronic inflammation, and unexplained pain whose issues trace back to muscle dysfunction — not just mechanical, but hormonal. Traditional approaches miss this connection. But understanding muscle as an endocrine organ unlocks powerful strategies for healing from the inside out, particularly when dealing with conditions like metabolic syndrome, autoimmune disease, chronic stress, and early hormonal decline.

The Science Behind It: Muscle as an Endocrine Organ

Anatomy and Molecular Physiology

Skeletal muscle comprises nearly 40% of total body mass and contains tens of thousands of myonuclei per fiber, each contributing to the tissue’s dynamic ability to adapt and signal. Beyond its mechanical function, skeletal muscle secretes a class of peptides called myokines, which act similarly to hormones. These myokines are released in response to muscle contraction and communicate with distant organs such as the liver, pancreas, brain, bones, adipose tissue, immune system, and even the ovaries.

This crosstalk is mediated by a group of well-studied myokines:

  • IL-6 (Interleukin-6): Once thought to be purely pro-inflammatory, muscle-derived IL-6 is anti-inflammatory and insulin-sensitizing when released during exercise. It upregulates GLP-1 from the gut and improves beta-cell insulin secretion in the pancreas.

  • Irisin: Cleaved from FNDC5, irisin triggers browning of white adipose tissue and upregulates BDNF (brain-derived neurotrophic factor) in the hippocampus, supporting learning, memory, and mood stability. Although animal and cell culture studies support irisin’s role in thermogenesis and BDNF regulation, the human data remain mixed due to inconsistencies in assay sensitivity. Nevertheless, irisin remains a key candidate in the muscle-brain axis.

  • Myostatin: A negative regulator of muscle growth. Elevated in sedentary individuals and associated with sarcopenia, obesity, and insulin resistance. Myostatin acts via the activin receptor type IIB (ActRIIB) pathway. Inhibition of ActRIIB has shown promising results in increasing muscle mass and improving glucose metabolism in early-phase clinical trials for sarcopenia and cachexia. However, long-term systemic inhibition must be approached cautiously due to potential off-target effects on reproductive and cardiac tissues.

  • IL-15: Promotes anabolic muscle signaling and enhances natural killer (NK) cell proliferation and immune regulation.

  • BDNF (Brain-Derived Neurotrophic Factor): Also produced by skeletal muscle during contraction, BDNF crosses the blood-brain barrier and supports neuronal plasticity.

Recent research also shows that muscle influences systemic metabolism via amino acid signaling, redox balance (e.g., glutathione), and mitochondrial adaptation. The more active and metabolically healthy your muscle, the stronger your entire endocrine network.

We now also understand that muscle communicates with reproductive tissues. Myokines such as irisin and myostatin regulate hypothalamic GnRH release, pituitary FSH production, and ovarian follicular health. These effects are sex-specific and modulated by estrogen and testosterone levels, adding another layer of complexity to how we understand exercise, fertility, and hormonal aging.

Not all movement stimulates these pathways equally.

Eccentric strength training, slow tempo sets, and metabolically demanding resistance work trigger greater myokine output — particularly IL-6, IGF-1, and BDNF — compared to steady-state cardio.

This is why proper program design matters. We don’t just get people moving — we train muscle as an endocrine tissue with structure, timing, and load precision to support hormonal function.

Symptom Patterns and Diagnostic Clues That Get Missed

Many patients — and unfortunately, many healthcare providers — focus solely on mechanical symptoms like pain, weakness, or tightness when evaluating muscle function. But because muscle is an endocrine organ, dysfunction here may manifest in systemic symptoms that don’t appear obviously “muscular.”

Commonly Overlooked Symptom Patterns:

  • Unexplained fatigue despite restful sleep and normal labs

  • Insulin resistance without significant weight gain

  • Mild depression, anxiety, or cognitive fog unrelated to life events

  • Worsening premenstrual symptoms or menstrual cycle irregularity

  • Exercise intolerance or prolonged post-exertional fatigue

  • Autoimmune flare-ups that do not fully resolve with immunosuppressants

  • Chronic low-grade inflammation despite an anti-inflammatory diet

  • Elevated uric acid or recurring gout attacks in people with lean body composition but reduced muscle mass

These symptoms often stem from dysfunctional or underutilized muscle mass. The endocrine signals that should be released with movement aren’t getting sent, and the downstream hormonal cascades involving insulin, estrogen, cortisol, and even thyroid hormone begin to misfire.

We also observe mitochondrial dysfunction and loss of oxidative flexibility in these individuals — particularly those with low resting muscle tone, cold extremities, and slow postural adjustments. These subtle signs often precede overt metabolic disease.

At Movability, we often identify these patterns by integrating orthopedic exams with hormone testing, myokine pathway analysis, and functional assessments of muscular endurance, capillary perfusion, and movement efficiency.

Who Benefits From This Approach

  • Women with early perimenopause, irregular cycles, or cognitive decline

  • Men with low testosterone, metabolic slowdown, or poor recovery

  • Individuals with unexplained fatigue, poor blood sugar control, or exercise intolerance

  • Anyone who feels worse when they try to work out “the right way”

  • People whose lab work looks normal but still feel off

  • Patients with chronic inflammation, gout, or elevated A1c that doesn’t respond to diet alone

If you’ve been trying to fix your hormones, energy, or metabolism — and nothing seems to stick — it’s time to consider the endocrine function of your muscle.

Movability’s Root-Cause Approach: Where Muscle Meets Metabolism

At Movability, we view muscle as one of the most intelligent endocrine tissues in the body. Our approach restores its signaling capabilities so it can resume its regulatory role.

How We Diagnose

  • Advanced neuromuscular screening: Identifies inhibited motor units, fascial restriction, and autonomic stress patterns.

  • Functional strength mapping: We use resistance tolerance, time-to-fatigue, and joint loading data to understand how effectively muscle contractions are stimulating myokine release.

  • Collaborative lab workups: Our naturopathic team evaluates estradiol, progesterone, cortisol curves, fasting insulin, SHBG, leptin, vitamin D, and uric acid to assess the metabolic environment in which muscle must operate.

  • Movement-integrated hormone strategy: We analyze whether certain muscles are underperforming in a way that contributes to hormonal resistance (e.g., underactive glutes reducing progesterone clearance via hepatic load).

How We Treat

  • Precision resistance training: To trigger specific myokine cascades like IL-6, irisin, and IGF-1 with minimal inflammatory cost.

  • Manual therapy and release techniques: To restore blood flow, decrease mechanoreceptor tension, and reactivate dormant tissue.

  • Targeted supplementation: Including magnesium bisglycinate, NFH Collagen SAP, fish oils, NAC, and adaptogens tailored to each patient’s cycle, cortisol rhythm, and recovery needs.

  • Tissue-focused nutrition: We prioritize leucine-rich proteins, creatine, and whole food sources of vitamin C to support connective tissue and hormonal regulation.

  • Lifestyle and circadian training: Sleep-wake rhythm is aligned to enhance cortisol-DHEA balance and melatonin secretion, amplifying muscle recovery.

Our team collaborates across chiropractic, physiotherapy, naturopathy, and massage therapy to continuously re-evaluate the body as it heals. This multidisciplinary integration is key to addressing the whole person, not just a set of symptoms.

Case Study #1: From Perimenopause to Hormonal Recovery

Background

A 36-year-old female patient came to us after being told by her OB-GYN that she was in perimenopause. She had declining estrogen levels, irregular periods, poor sleep, brain fog, and new-onset insulin resistance despite no change in weight. She had also recently stopped weight training due to joint pain and fatigue.

What Was Missed

Her estrogen wasn’t declining because of ovarian failure. It was declining because of:

  • Loss of muscle mass due to inactivity

  • Increased aromatization of estrogen into inflammatory metabolites due to visceral fat gain

  • Low IL-6 and BDNF signaling due to lack of movement, impairing feedback loops to the hypothalamus

  • Chronically high cortisol flattening her luteinizing hormone (LH) surge

No one had looked at her neuromuscular patterns or muscle-endocrine interactions.

Our Intervention

We designed a collaborative program involving:

  • Soft tissue therapy and dry needling to reduce glute and spinal tension

  • A resistance reintroduction program focused on eccentric control and time under tension

  • Vitamin D, magnesium bisglycinate, collagen, and NAC to reduce inflammatory signaling

  • BDNF-stimulating breathwork and daily infrared walks to improve vagal tone and cognitive clarity

  • Functional lab tracking of estrogen metabolites, cortisol rhythm, SHBG, and DHEA over 3 months

Results

Within 12 weeks:

  • Her periods normalized

  • Brain fog resolved

  • Fasting insulin and HOMA-IR returned to healthy ranges

  • Muscle tone and energy improved

  • Estradiol and progesterone levels stabilized naturally

She no longer met the criteria for perimenopause. Instead of hormone replacement, we gave her back the muscle signal that drives hormonal balance from the ground up.

Case Study #2: Reversing Early Diabetes, Gout, and Low Testosterone in a 43-Year-Old Male

Background

A 43-year-old male came to Movability with persistent fatigue, low libido, poor exercise recovery, and recurrent gout attacks. He had gained 10 lbs in the past year despite no dietary change. Bloodwork revealed:

  • HbA1c at 6.2% (prediabetic)

  • Low-normal testosterone (total T: 340 ng/dL)

  • Elevated uric acid and borderline creatinine

He had tried low-carb diets and over-the-counter testosterone boosters without sustained improvement.

What Was Missed

  • Loss of muscle mass reduced his ability to clear glucose, driving insulin resistance

  • Low physical activity and irregular circadian rhythm impaired LH and testosterone output

  • High myostatin and low IL-6/IL-15 impaired mitochondrial signaling and fat metabolism

  • Reduced creatine phosphate buffering may have increased purine turnover and uric acid load

No clinician had addressed the muscle-endocrine interface or his circadian inflammation cycle.

Our Intervention

  • Reintroduced strength training with progressive resistance under physiotherapy supervision

  • Manual therapy and diaphragmatic release to normalize sympathetic tone and reduce cortisol

  • Creatine monohydrate (3g/day), magnesium, omega-3s, and berberine

  • Whole food plan centered around muscle-sparing protein intake, tart cherries, and ginger to lower uric acid and reduce inflammation

  • Sleep tracking and morning light exposure to restore diurnal cortisol-testosterone rhythm

Results

Within 4 months:

  • HbA1c dropped from 6.2% to 5.5%

  • Total testosterone rose from 340 to 470 ng/dL

  • Gout attacks stopped

  • Muscle definition returned, along with improved motivation and libido

Follow-up testing at the 4-month mark confirmed improvements in HbA1c, testosterone, and uric acid, aligning with patient-reported gains in energy, libido, and physical performance. All labs were carefully monitored and interpreted by our in-house naturopath, who adjusted diet, supplementation, and lifestyle interventions accordingly.

These results reflect just one of many cases where rebuilding muscle endocrine signaling — in collaboration with our in-house naturopath — has helped patients normalize lab values and regain metabolic control without relying on medication.

Muscle Health Is Hormone Health

Understanding skeletal muscle as an endocrine organ is one of the most important paradigm shifts in modern healthcare. Whether you’re dealing with fatigue, early perimenopause, gout, insulin resistance, brain fog, or chronic inflammation, your muscles may be silently contributing to the problem — or the solution.

At Movability, we combine in-depth diagnostics, interdisciplinary care, and cutting-edge therapies to restore your muscle’s ability to regulate your hormones, your metabolism, and your mind.

Contact Movability today to book a comprehensive assessment and experience our results-driven approach.

Sina Yeganeh