Free Testosterone Impact quantifies the direct, biologically active influence of the unbound fraction of testosterone on target tissues throughout the body. Unlike total testosterone, which includes hormone bound to SHBG and albumin, the free fraction is immediately available to diffuse into cells and bind to androgen receptors, initiating physiological effects. This impact is the true driver of male and female characteristics, including muscle mass maintenance, bone density, libido, and neurocognitive function. Therefore, clinical focus on the free level provides a more accurate assessment of androgenic status.
Origin
The concept originated from the realization in endocrinology that total hormone levels often do not correlate perfectly with clinical symptoms, leading to the development of the “free hormone hypothesis.” This hypothesis posits that only the unbound fraction of a steroid hormone is physiologically relevant. The term emphasizes the functional significance of this bioavailable fraction.
Mechanism
Free testosterone diffusess across the cell membrane, bypassing the need for transport proteins, and binds directly to intracellular androgen receptors (AR). The activated AR-hormone complex then translocates to the nucleus, where it binds to specific DNA sequences to modulate gene transcription. This genomic action leads to the synthesis of new proteins that mediate the diverse anabolic and neuroendocrine effects attributed to testosterone.
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