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Fundamentals

The decision to cease a hormonal optimization protocol, such as Testosterone Replacement Therapy (TRT), often brings a particular kind of silence. It is the quiet period after the external support has been removed, a space where you are waiting for your own biological systems to resume their natural rhythm.

This experience of waiting, of feeling the lag between the cessation of therapy and the return of your innate vitality, is a direct, physical manifestation of a complex internal recalibration. You are not merely waiting; your body is actively working to re-establish a sophisticated communication network that governs energy, mood, and overall function. Understanding the architecture of this system is the first step toward actively participating in its recovery.

At the center of this process is a remarkable biological system known as the Hypothalamic-Pituitary-Gonadal (HPG) axis. This is the body’s primary command and control structure for hormonal health. Think of it as a highly responsive, three-part orchestra. The hypothalamus, a small region at the base of the brain, acts as the conductor.

It senses the body’s needs and, in response, sends out a rhythmic pulse of a signaling molecule called Gonadotropin-Releasing Hormone (GnRH). This is the conductor’s beat, setting the tempo for the entire system.

The GnRH signal travels a very short distance to the pituitary gland, the orchestra’s lead violinist. Upon receiving the GnRH pulse, the pituitary plays its part by releasing two other crucial hormones into the bloodstream ∞ Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH).

These are the melodies that travel throughout the body to their target audience, the gonads (the testes in men). When the testes receive the LH signal, they respond by producing testosterone. This entire sequence is a delicate feedback loop.

As testosterone levels rise, the hypothalamus and pituitary gland detect this, and the conductor slows the GnRH beat, which in turn quiets the pituitary’s melody, ensuring that hormonal levels remain within a healthy, balanced range. It is a system of elegant self-regulation.

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How Hormonal Protocols Create a Pause

When you introduce exogenous testosterone during a TRT protocol, you are essentially bringing in a powerful, outside sound system that plays the final musical piece ∞ abundant testosterone ∞ very loudly. The conductor (the hypothalamus) and the lead violinist (the pituitary) perceive this loud, constant sound. Their logical response is to cease their own production.

They sense that more than enough testosterone is present, so the GnRH beat stops, and the LH and FSH melodies fall silent. This state of suppression is a normal and expected consequence of the therapy. The HPG axis is not broken; it has simply gone into a dormant state because its function was being performed by an external source.

The challenge of post-TRT recovery arises from this dormancy. Once the external testosterone is removed, there is a period of silence. The body’s natural production has been offline, and it requires time and specific inputs to reawaken the conductor and coax the orchestra back into playing.

This is where lifestyle adjustments become so powerful. They are the tools you can use to send the first gentle signals back to the hypothalamus, encouraging it to pick up its baton and begin the GnRH rhythm once more.

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The Four Pillars of System Reactivation

Supporting your body’s return to its own hormonal music involves providing the foundational elements that the HPG axis requires to function optimally. These can be understood as four interconnected pillars of support. Each one provides a different set of resources and signals that encourage the system to come back online with stability and efficiency.

  • Nutritional Resourcing ∞ Your endocrine system cannot build hormones from nothing. It requires a consistent supply of specific raw materials. Macronutrients like healthy fats and proteins are the fundamental building blocks for steroid hormones, including testosterone. Micronutrients, such as certain vitamins and minerals, act as the essential cofactors or “tools” that facilitate the biochemical reactions of hormone synthesis. A nutrient-dense diet provides the complete toolkit for hormonal production.
  • Movement Signaling ∞ Physical activity, particularly resistance training, does more than build muscle. It sends powerful signals throughout the body that communicate a need for strength, repair, and adaptation. This demand encourages the hormonal systems to respond. Exercise improves cellular sensitivity to hormones, meaning the messages that are sent are heard more clearly. It is a way of priming the entire system to listen for the returning signals of the HPG axis.
  • Restorative Sleep ∞ The majority of the body’s repair and regulation processes occur during sleep. It is during the deep stages of sleep that the hormonal environment is reset. The pituitary gland is highly active during this time, producing key hormones. Chronic sleep disruption interferes with this restorative cycle, particularly affecting the balance between stress hormones and reproductive hormones. Quality sleep is non-negotiable for allowing the HPG axis the quiet, dedicated time it needs to recalibrate.
  • Stress Modulation ∞ The body has another major hormonal axis, the Hypothalamic-Pituitary-Adrenal (HPA) axis, which governs the stress response. This system and the HPG axis exist in a delicate balance. Chronic stress leads to sustained high levels of the hormone cortisol, which can directly suppress the function of the HPG axis. The conductor (hypothalamus) cannot effectively lead the reproductive orchestra when it is constantly being drowned out by stress alarms. Managing stress is essential to creating the calm internal environment needed for hormonal recovery.

These four pillars work together to create a biological environment that is conducive to recovery. They provide the raw materials, the signaling, the restorative time, and the calm operational space for your internal orchestra to begin playing its own music once again. The goal is a return to a state of self-regulating vitality, guided by your own biology.


Intermediate

Transitioning away from therapeutic hormonal support requires a shift in perspective. The focus moves from providing an external solution to cultivating an internal environment that encourages the body’s own endocrine systems to resume their sophisticated duties. Lifestyle adjustments in this context are precise interventions designed to support the complex biochemistry of the Hypothalamic-Pituitary-Gonadal (HPG) axis. By strategically managing nutrition, exercise, sleep, and stress, you can supply the specific substrates and stimuli that facilitate this delicate recalibration process.

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Nutritional Protocols for Hormonal Precursors

The production of testosterone is a multi-step biochemical process known as steroidogenesis, and it begins with cholesterol. Providing your body with the right dietary components is fundamental to ensuring this assembly line runs efficiently. A diet structured for hormonal recovery is built on nutrient density and specific macronutrient and micronutrient profiles.

A dietary framework resembling the Mediterranean pattern is highly effective. This approach emphasizes whole foods, including an abundance of vegetables, fruits, lean proteins, and healthy fats. Monounsaturated and saturated fats, found in foods like avocados, olive oil, nuts, seeds, and responsibly sourced animal products, are particularly important as they provide the cholesterol backbone required for hormone synthesis. It is a biological prerequisite; without adequate healthy fat intake, the primary building blocks for testosterone are simply unavailable.

By supplying the correct dietary fats and micronutrients, you directly provide the raw materials for the body’s hormone production pathways.

Beyond fats, specific micronutrients function as critical catalysts in the hormonal cascade. Zinc, for instance, is directly involved in the function of enzymes that synthesize testosterone. A deficiency in zinc can impede this process at a foundational level. Similarly, Vitamin D receptors are found in the cells of the testes that produce testosterone, indicating its direct role in hormonal regulation.

Magnesium contributes by modulating the activity of Sex Hormone-Binding Globulin (SHBG), a protein that binds to testosterone in the blood. By managing SHBG, more testosterone can remain in its “free” or bioavailable state, able to interact with cells.

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Key Micronutrients for HPG Axis Support

Micronutrient Role in Hormonal Health Dietary Sources
Zinc Acts as a cofactor for enzymes essential in testosterone synthesis. Supports LH production from the pituitary gland. Oysters, beef, pumpkin seeds, lentils, shiitake mushrooms.
Vitamin D Functions as a steroid hormone itself. Receptors are present in hypothalamic, pituitary, and testicular tissues, suggesting a direct regulatory role. Fatty fish (salmon, mackerel), fortified milk, egg yolks, sun exposure.
Magnesium Helps to increase free testosterone levels by reducing the binding affinity of SHBG. Supports overall enzymatic function and cellular energy. Spinach, almonds, cashews, dark chocolate, avocados.
Selenium Essential for sperm production and motility. Acts as a powerful antioxidant, protecting testicular cells from oxidative stress. Brazil nuts, tuna, sardines, beef, chicken, eggs.
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What Is the Best Exercise Protocol for Hormonal Recovery?

Physical activity is a potent modulator of the endocrine system. Different forms of exercise send distinct signals to the body, eliciting specific hormonal and metabolic responses. For post-TRT recovery, a combination of resistance training and high-intensity interval training (HIIT) appears to be most beneficial.

Resistance training, such as weightlifting, creates a significant stimulus for adaptation. The mechanical tension placed on muscle fibers activates a cascade of signaling pathways that promote tissue repair and growth. This process involves the upregulation of androgen receptors in muscle cells, making them more sensitive to the testosterone that the body begins to produce.

A system with more sensitive receptors requires less hormonal output to achieve a physiological effect, creating a more efficient endocrine environment. Sessions should focus on large, compound movements like squats, deadlifts, presses, and rows to engage the maximum amount of muscle mass.

High-Intensity Interval Training (HIIT) offers a complementary benefit. These short bursts of intense effort followed by brief recovery periods are exceptionally effective at improving metabolic health, particularly insulin sensitivity. Poor insulin sensitivity, or insulin resistance, is linked to lower testosterone levels. HIIT helps improve how the body manages blood sugar, reducing the chronic inflammation and metabolic dysfunction that can burden the HPG axis. This can be incorporated through activities like sprinting, cycling, or rowing.

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Comparing Exercise Modalities

Exercise Type Primary Mechanism Hormonal Impact Recommended Frequency
Resistance Training Induces muscle protein synthesis and increases androgen receptor density. Acutely increases testosterone and growth hormone post-exercise. Improves long-term hormonal signaling efficiency. 3-4 times per week, focusing on major muscle groups.
HIIT Improves mitochondrial function and insulin sensitivity. Can boost testosterone production and helps lower cortisol over time. Reduces metabolic stress on the endocrine system. 1-2 times per week, as an adjunct to resistance training.
Moderate Aerobic Enhances cardiovascular health and aids in body fat management. Indirectly supports hormonal health by reducing excess body fat, which can decrease aromatase activity (the conversion of testosterone to estrogen). 2-3 times per week, for overall health and weight management.
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Sleep Architecture and Stress Axis Regulation

The architecture of your sleep is profoundly linked to the function of your hormonal systems. The nightly journey through different sleep stages is when the body performs its most critical regulatory work. The majority of Growth Hormone (GH) is released during slow-wave sleep (deep sleep).

This stage is also when the Hypothalamic-Pituitary-Adrenal (HPA) axis, our stress system, is maximally inhibited. This down-regulation of the HPA axis is vital for HPG recovery because the two systems operate in a reciprocal balance. Chronic activation of the stress axis, with its high output of cortisol, directly suppresses GnRH release from the hypothalamus.

Therefore, optimizing sleep is a direct strategy for optimizing HPG axis function. This involves cultivating consistent sleep hygiene practices.

  • Consistent Schedule ∞ Go to bed and wake up at the same time each day, even on weekends, to anchor your body’s circadian rhythm.
  • Light Exposure ∞ Get bright light exposure, preferably from the sun, in the morning to signal wakefulness. Avoid bright screens and overhead lights in the 1-2 hours before bed to allow for natural melatonin production.
  • Cool, Dark, Quiet Environment ∞ Create a bedroom environment that minimizes disruptions. A cool room temperature is particularly conducive to deep sleep.
  • Limit Stimulants ∞ Avoid caffeine after the early afternoon and be mindful of alcohol consumption, as it can disrupt the second half of the night’s sleep architecture.

By prioritizing sleep, you are creating the ideal neurochemical conditions for the hypothalamus to resume its rhythmic signaling, free from the suppressive interference of an overactive stress response. This allows the delicate process of hormonal recovery to proceed on schedule.


Academic

The recovery of endogenous testosterone production following the cessation of androgenic-anabolic steroid use or TRT is a complex physiological process governed by the reactivation of the Hypothalamic-Pituitary-Gonadal (HPG) axis. While post-cycle therapy (PCT) protocols involving agents like Selective Estrogen Receptor Modulators (SERMs) or hCG are common clinical strategies, the underlying biological environment dictates their efficacy.

Lifestyle interventions, far from being mere adjunctive support, are potent modulators of the neuroendocrine and metabolic systems that underpin HPG axis function. A deep examination reveals that the interplay between the HPG axis and the Hypothalamic-Pituitary-Adrenal (HPA) axis is a central determinant of recovery outcomes.

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Neuroendocrine Crosstalk the HPG and HPA Axis Interface

The HPG and HPA axes are the body’s primary conduits for reproduction and stress adaptation, respectively. They are intricately linked, sharing anatomical space in the hypothalamus and pituitary and exhibiting a functionally antagonistic relationship.

The principal mediator of the HPA axis, Corticotropin-Releasing Hormone (CRH), not only initiates the stress cascade leading to cortisol release but also exerts a direct inhibitory effect on the HPG axis. Elevated CRH, a hallmark of chronic physiological or psychological stress, has been shown to suppress the pulsatility of Gonadotropin-Releasing Hormone (GnRH). This suppression occurs at the level of the hypothalamus, effectively silencing the initial signal required to stimulate the pituitary.

Furthermore, the end product of the HPA cascade, cortisol, reinforces this suppression. Glucocorticoids can reduce the pituitary’s sensitivity to GnRH and directly inhibit testosterone synthesis within the testicular Leydig cells. From a systems-biology perspective, this makes teleological sense ∞ in a state of chronic threat (as signaled by high cortisol), the body deprioritizes metabolically expensive, long-term functions like reproduction in favor of immediate survival.

During post-TRT recovery, a state of HPA axis hyperactivity can therefore present a significant barrier to HPG reactivation. Lifestyle strategies that modulate the HPA axis, such as mindfulness meditation, controlled breathing exercises, and adequate sleep, function to lower CRH and cortisol tone, thereby removing the inhibitory brake on the HPG axis.

The state of the body’s stress-response system directly governs the permissive environment required for the reproductive axis to recover.

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How Does Metabolic Health Dictate Hormonal Bioavailability?

Metabolic health, particularly insulin sensitivity, is another critical factor influencing the hormonal milieu. Insulin resistance, often driven by a sedentary lifestyle and a diet high in processed carbohydrates, has profound implications for testosterone bioavailability. One key mechanism involves Sex Hormone-Binding Globulin (SHBG), a glycoprotein produced primarily in the liver that binds to sex hormones, rendering them biologically inactive. High circulating insulin levels, characteristic of insulin resistance, suppress the liver’s production of SHBG.

While lower SHBG might initially seem beneficial by increasing the proportion of free testosterone, in the context of a recovering HPG axis, the net effect can be detrimental. The total testosterone pool is already low, and the body’s feedback mechanisms are highly sensitive to the concentration of free hormones.

A lower SHBG level means that even a small amount of newly produced testosterone is more readily available to tissues and to the hypothalamus and pituitary for feedback inhibition. This can prematurely signal to the HPG axis that levels are sufficient, potentially blunting the drive for further production.

Lifestyle interventions that improve insulin sensitivity, such as resistance training, HIIT, and a low-glycemic, fiber-rich diet, help to normalize SHBG levels. This creates a more stable hormonal transport system, allowing for a more robust and sustained recovery of total testosterone production before negative feedback mechanisms are fully engaged.

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The Cellular Environment Nutrition’s Role in Enzymatics and Inflammation

At the most granular level, hormonal recovery depends on cellular health and enzymatic function. The synthesis of testosterone from cholesterol is a cascade of enzymatic conversions. These enzymes require specific micronutrient cofactors to function correctly. For example, the conversion of testosterone to dihydrotestosterone (DHT) is catalyzed by the 5-alpha reductase enzyme, a process that is zinc-dependent.

The aromatase enzyme, which converts testosterone to estradiol, is also a key regulatory point. While some estradiol is necessary for male health, excessive aromatase activity, common in states of obesity and inflammation, can deplete the testosterone pool and increase estrogenic feedback at the pituitary.

Systemic inflammation acts as a potent disruptor of this delicate balance. Pro-inflammatory cytokines, such as Interleukin-6 (IL-6) and Tumor Necrosis Factor-alpha (TNF-α), can suppress Leydig cell function and contribute to HPA axis activation. A diet rich in omega-3 fatty acids (from fatty fish), polyphenols (from colorful plants), and antioxidants helps to mitigate systemic inflammation.

This creates a less hostile cellular environment for the testes to resume their steroidogenic function. In contrast, a diet high in processed foods, refined sugars, and industrial seed oils promotes a pro-inflammatory state that works directly against HPG axis recovery.

A nutrient-dense, anti-inflammatory diet provides the essential cofactors for hormone synthesis while reducing the systemic static that interferes with endocrine signaling.

Ultimately, lifestyle adjustments provide a multi-faceted therapeutic approach to post-TRT recovery. They work to quiet the suppressive noise from the HPA axis, optimize the metabolic environment for hormone transport and bioavailability, and provide the direct cellular and enzymatic support required for steroidogenesis. These interventions create a physiological foundation upon which pharmacological strategies like SERM therapy can act with greater efficacy, facilitating a more complete and stable return to endogenous hormonal function.

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References

  • Lykhonosov, M. P. et al. “.” Problemy Endokrinologii, vol. 66, no. 4, 2020, pp. 58-66.
  • Handa, R. J. and M. J. Weiser. “Role of HPA and the HPG-axis interaction in testosterone-mediated learned helpless behavior.” Frontiers in Endocrinology, vol. 5, 2014, p. 157.
  • Zamir, A. et al. “Diet and exercise in management of low testosterone.” One Health Ohio, 2021.
  • Vgontzas, A. N. et al. “Sleep deprivation effects on the activity of the hypothalamic-pituitary-adrenal and growth axes ∞ potential clinical implications.” The Journal of Clinical Endocrinology & Metabolism, vol. 84, no. 5, 1999, pp. 1595-1601.
  • Leproult, R. and E. Van Cauter. “Role of sleep and sleep loss in hormonal release and metabolism.” Endocrine Reviews, vol. 31, no. 2, 2010, pp. 157-175.
  • Shoskes, J. J. et al. “Clomiphene citrate for the treatment of testosterone deficiency.” The Journal of Urology, vol. 193, no. 3, 2015, pp. 935-940.
  • Bhattacharya, R. K. and K. K. Krori. “The effect of exogenous testosterone on the HPG axis.” ResearchGate, 2016.
  • Whitten, M. D. et al. “The effect of diet and exercise on testosterone levels in men.” Journal of Andrology, vol. 33, no. 5, 2012, pp. 841-848.
  • Pilz, S. et al. “Effect of vitamin D supplementation on testosterone levels in men.” Hormone and Metabolic Research, vol. 43, no. 3, 2011, pp. 223-225.
  • Te, L. B. and J. M. Liu. “The effect of resistance exercise on the testosterone response in men.” Journal of Strength and Conditioning Research, vol. 27, no. 5, 2013, pp. 1435-1441.
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Reflection

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A Return to Self Regulation

The information presented here offers a map of the biological terrain you must navigate during hormonal recovery. It details the communication pathways, the necessary resources, and the potential roadblocks within your own physiology. This knowledge transforms the passive act of waiting into a period of active, intentional cultivation. Each meal, each workout, and each night of restful sleep becomes a deliberate contribution to the restoration of your body’s innate capacity for vitality.

The journey back to endogenous hormonal balance is a personal one. Your unique genetic makeup, health history, and life circumstances will all shape the timeline and texture of your recovery. The principles outlined provide a robust framework, yet the application must be tailored to your individual experience.

This process invites a deeper awareness of your body’s signals. It is an opportunity to listen to what your system needs and to respond with precise, supportive action. The ultimate goal is to re-establish a resilient, self-regulating system that functions with inherent strength, guided by your own biological intelligence.

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Glossary

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hormonal optimization

Meaning ∞ Hormonal Optimization is a clinical strategy for achieving physiological balance and optimal function within an individual's endocrine system, extending beyond mere reference range normalcy.
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gonadotropin-releasing hormone

Meaning ∞ Gonadotropin-Releasing Hormone, or GnRH, is a decapeptide hormone synthesized and released by specialized hypothalamic neurons.
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gnrh

Meaning ∞ Gonadotropin-releasing hormone, or GnRH, is a decapeptide produced by specialized neurosecretory cells within the hypothalamus of the brain.
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pituitary gland

Meaning ∞ The Pituitary Gland is a small, pea-sized endocrine gland situated at the base of the brain, precisely within a bony structure called the sella turcica.
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testosterone levels

Meaning ∞ Testosterone levels denote the quantifiable concentration of the primary male sex hormone, testosterone, within an individual's bloodstream.
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hpg axis

Meaning ∞ The HPG Axis, or Hypothalamic-Pituitary-Gonadal Axis, is a fundamental neuroendocrine pathway regulating human reproductive and sexual functions.
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post-trt recovery

Meaning ∞ Post-TRT Recovery refers to the physiological process where the body’s endogenous testosterone production system, the Hypothalamic-Pituitary-Testicular Axis, attempts to regain natural function after cessation of exogenous testosterone replacement therapy.
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lifestyle adjustments

Meaning ∞ Lifestyle adjustments are deliberate modifications to daily habits and environmental factors.
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resistance training

Meaning ∞ Resistance training is a structured form of physical activity involving the controlled application of external force to stimulate muscular contraction, leading to adaptations in strength, power, and hypertrophy.
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hormonal recovery

Meaning ∞ Hormonal recovery denotes the physiological process or clinical intervention focused on re-establishing optimal endocrine system function and restoring hormone levels to a healthy physiological range.
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steroidogenesis

Meaning ∞ Steroidogenesis refers to the complex biochemical process through which cholesterol is enzymatically converted into various steroid hormones within the body.
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insulin sensitivity

Meaning ∞ Insulin sensitivity refers to the degree to which cells in the body, particularly muscle, fat, and liver cells, respond effectively to insulin's signal to take up glucose from the bloodstream.
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hpa axis

Meaning ∞ The HPA Axis, or Hypothalamic-Pituitary-Adrenal Axis, is a fundamental neuroendocrine system orchestrating the body's adaptive responses to stressors.
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endogenous testosterone

Meaning ∞ Endogenous testosterone refers to the steroid hormone naturally synthesized within the human body, primarily by the Leydig cells in the testes of males and in smaller quantities by the ovaries and adrenal glands in females.
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testosterone production

Meaning ∞ Testosterone production refers to the biological synthesis of the primary male sex hormone, testosterone, predominantly in the Leydig cells of the testes in males and, to a lesser extent, in the ovaries and adrenal glands in females.
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leydig cell function

Meaning ∞ Leydig cell function denotes the specialized role of interstitial Leydig cells in the testes, primarily synthesizing and secreting androgenic steroids, predominantly testosterone.