For discussing the functions of different structures of all organisms.
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Estrogen is not one hormone, it is the name used to denote either of two steroid hormones. These hormones are noted for their role in the development of the secondary sexual characteristics of females. In mammals the most abundant (and most potent) estrogen is estradiol (a dialcohol: note the "-diol" suffix), followed by estrone (a
ketone : note the -one suffix). As is true for the other steroid hormones, the major biosynthetic pathway for estrogen begins with
cholesterol (C27). The figure shows the major metabolic intermediates in the usual synthesis of estrogen, starting with cholesterol, proceeding to
pregnenolone (C21), an androgen (C19), and then estrogen (C18). Estrogen has an alcohol functional group at the C3 and C17 positions, and a methyl group at C13. A unique aspect of estrogen biosynthesis is the conversion (catalyzed by the enzyme aromatase) of the A ring to an aromatic ring.
Estrogen is produced in the ovaries and secreted into the blood, whereupon it enters target cells throughout the body. It enters the cells via passive diffusion and binds to specific proteins called estrogen receptors,which reside in the cell nuclei. In the absence of estrogen, these receptors are functionally inactive. The binding of estrogen to a receptor activates the receptor, which can then bind to specific sites on the DNA to stimulate the transcription of a highly specific set of genes. As a result, the metabolism and the character of the cell changes.
In addition to its role in the development of the secondary sex characteristics in females, estrogen has important physiological functions in the cardiovascular, immune, and central nervous systems, as well as its effects on the growth and maturation of the long bones. It is also implicated in a number of diseases (including breast and uterine cancers) and in postmenopausal health problems, such as atherosclerosis, osteoporosis, and diminution of cognitive functions. Because these conditions, especially female cancers, are associated with estrogen, a number of anticancer treatments involve estrogen blockade: drugs that prevent estrogen from binding to its receptors. As a result, the receptors remain in an inactive form.
I am actually quite interested in the (maybe unspecific?) effects of estrogens in the lipid bilayer. As a steroid it can easily slip through any membrane - but will it accumulate there and modify the bilayer? Is it possible that it induces structural changes of membrane associated proteins or ion channels?
I'd be happy about any input from you!
Well I'll say Chenn's article was interesting. Not sure what the purpose of posting it was, and it seems like it might just be a cut-and-paste, since there is a reference to a picture or diagram.
What did the parasitic Candiru fish say when it finally found a host? - - "Urethra!!"
5 posts • Page 1 of 1
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