The Steroid Hormones

Boswell,making use of the methodology elaborated by Martin and Kagan, prepared a series of 6,6-difluoro-A -3-ketones closely related to the steroid hormones, exemplified by the conversion of 3)5,17a-dihydroxypregn-5-en-20-one diacetate (7) to 6,6-difluoro-17a-acetoxyprogesterone (12). Reaction of (7) with nitrosyl fluoride at 0° affords the nitrimine (8), which is... 

FIGURE 25.43 The steroid hormones are synthesized from cholesterol, with intermediate formation of pregnenolone and progesterone. Testosterone, the principal male sex hormone steroid, is a precursor to /3-estradiol. Cortisol, a glucocorticoid, and aldosterone, a mineralocorticoid, are also derived from progesterone. 

The first step of the Robinson annulation is simply a Michael reaction. An enamine or an enolate ion from a jS-keto ester or /3-diketone effects a conjugate addition to an a-,/3-unsaturated ketone, yielding a 1,5-diketone. But as we saw in Section 23.6,1,5-diketones undergo intramolecular aldol condensation to yield cyclohexenones when treated with base. Thus, the final product contains a six-membered ring, and an annulation has been accomplished. An example occurs during the commercial synthesis of the steroid hormone estrone (figure 23.9). 

Figure 23.9 This Robinson annulation reaction is used in the commercial synthesis of the steroid hormone estrone. The nucleophilic donor is a /3-diketone.

You should have predicted that the sterols are present in greatest quantity in biological systems. Your knowledge of biology should have enabled you to identify the steroid hormones as being present in lowest concentrations since hormone, in general, are effective at very low concentrations. 

Again, the answer should be fairly obvious. The potential therapeutic value of the steroid hormones makes these of tremendous commercial value. The commercial market for these is of the order of hundreds of millions of dollars per year. There is no comparable market for sterols and bile salts. We are faced with the interesting situation, therefore, that sterols are relatively abundant in natural sources but of relatively low commercial value, whilst steroids occur naturally at very low concentrations but are of great commercial value. Although there are tremendous variations amongst different products, steroids with desirable properties command market prices that are (ten to one thousand fold) greater than their sterol counterparts. 

The steroid hormone 1,25-dihydroxy vitamin D3 (calcitriol) slowly increases both intestinal calcium absorption and bone resorption, and is also stimulated through low calcium levels. In contrast, calcitonin rapidly inhibits osteoclast activity and thus decreases serum calcium levels. Calcitonin is secreted by the clear cells of the thyroid and inhibits osteoclast activity by increasing the intracellular cyclic AMP content via binding to a specific cell surface receptor, thus causing a contraction of the resorbing cell membrane. The biological relevance of calcitonin in human calcium homeostasis is not well established. 

Sex steroid receptors are members of the steroid hormone receptor (SHR) family that ligand-dependently regulate functions of the sexual organs. Sex steroid receptors are the androgen receptor [1] (AR), the estrogen receptor a [2] and (3 [3] (ERa, ER 3), and the progesterone receptor [4] (PR). 

The column used was 25 cm long, 4.6 mm in diameter, and packed with silica gel particle (diameter 5 pm) giving an maximum efficiency at the optimum velocity of 25,000 theoretical plates. The mobile phase consisted of 76% v/v n-hexane and 24% v/v 2-propyl alcohol at a flow-rate of 1.0 ml/min. The steroid hormones are mostly weakly polar and thus, on silica gel, will be separated primarily on a basis of polarity. The silica, however, was heavily deactivated by a relatively high concentration of the moderator 2-propyl alcohol and thus the interacting surface would be covered with isopropanol molecules. Whether the interaction is by sorption or displacement is difficult to predict. It is likely that the early peaks interacted by sorption and the late peaks by possibly by displacement. 

H)2-D3 is produced by a complex series of enzymatic reactions that involve the plasma transport of precursor molecules to a number of different tissues (Figure 42-9). One of these precursors is vitamin D—really not a vitamin, but this common name persists. The active molecule, l,25(OH)2-D3, is transported to other organs where it activates biologic processes in a manner similar to that employed by the steroid hormones. 

As mentioned above, the steroid hormones and 1,25(0H)2-D3 are synthesized in their final active form. They are also secreted as they are made, and thus... 

A most important function of vitamin A is in the control of cell differentiation and mrnover. PsA-trans-retinoic acid and 9-cw-retinoic acid (Figure 45-1) regulate growth, development, and tissue differentiation they have different actions in different tissues. Like the steroid hormones and vitamin D, retinoic acid binds to nuclear receptors that bind to response elements of DNA and regulate the transcription of specific genes. There are two families of nuclear retinoid receptors the retinoic acid receptors (RARs) bind all-rrijw-retinoic acid or 9-c -retinoic acid, and the retinoid X receptors (RXRs) bind 9-cw-retinoic acid. 

Amine hormones include the thyroid hormones and the catecholamines. The thyroid hormones tend to be biologically similar to the steroid hormones. They are mainly insoluble in the blood and are transported predominantly (>99%) bound to proteins. As such, these hormones have longer half-lives (triiodothyronine, t3, = 24 h thyroxine, T4, = 7 days). Furthermore, thyroid hormones cross cell membranes to bind with intracellular receptors and may be administered orally (e.g., synthryoid). In contrast to steroid hormones, however, thyroid hormones have the unique property of being stored extra-cellularly in the thyroid gland as part of the thyroglobulin molecule. 

Cholesterol is the parent of all of the steroid hormones and bile acids in the... 

The steroid hormones known as mineralocorticoids and glucocorticoids are synthesized in the adrenal cortex of mammals [3]. The physiological mineralocorticoid is... 

Several criteria determine whether a steroid-hormone-binding site is a putative receptor. First, the steroid-hormone-binding site must be present in hormone-responsive tissues or brain regions, and absent from nonresponsive ones. Second, it should bind steroids that are either active agonists or effective antagonists of the hormone effect, and should not bind steroids that are inactive in either sense. 

Steroid hormones regulate a very extensive assembly of functions in numerous corporal tissues. Estrogens, the steroid hormones to which the majority of this chapter is dedicated, regulate from basic functions related to reproduction, the development of the skeleton, the maintenance of arterial tension, or diverse nervous functions. The molecular studies on the mechanism of action of estrogens have set the foundations that will permit us to understand how they carry out such diverse functions in such dissimilar tissues as well as how some substances that act through the estrogen signaling pathway can exercise opposite functions in different tissues. In this respect, there are five facts of particular importance that constitute the central nucleus of this revision ... 

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