The physiological distribution and ratio of a specific hormone that is unbound, or free, versus the portion that is bound to carrier proteins, such as Sex Hormone-Binding Globulin (SHBG) or albumin, in the bloodstream. Only the free fraction of a hormone is biologically active and capable of diffusing into tissues to exert its effect on target cells. Clinical assessment of partitioning is critical because total hormone levels can be misleading if the proportion of free, active hormone is compromised by altered carrier protein levels.
Origin
This principle is foundational to clinical endocrinology and pharmacology, stemming from the understanding of protein-hormone interactions in plasma. The term ‘partitioning’ refers to the division or distribution of the hormone between the bound and unbound compartments. It is an essential concept for accurately assessing hormonal bioavailability and predicting the true clinical effect of a hormone on the body’s systems.
Mechanism
Hormone partitioning is mechanistically determined by the concentration and affinity of the carrier proteins, primarily SHBG, which binds sex steroids like testosterone and estradiol with high affinity. Factors that influence SHBG production, such as insulin levels, thyroid function, and liver health, directly impact the free hormone fraction. The dynamic equilibrium between bound and free hormone ensures a stable supply of active hormone to target cells despite fluctuations in total circulating levels.
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