EMERGING DIVERSITIES IN THE MECHANISM OF ACTION OF STEROID-HORMONES

被引:223
作者
BRANN, DW [1 ]
HENDRY, LB [1 ]
MAHESH, VB [1 ]
机构
[1] MED COLL GEORGIA, DEPT PHYSIOL & ENDOCRINOL, AUGUSTA, GA 30912 USA
关键词
D O I
10.1016/0960-0760(94)00160-N
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The classical genomic action of steroid hormones acting through intracelluar receptors is well recognized. within this concept of action, questions regarding the ultimate fate of the hormone and lack of a tight correlation between tissue uptake and biological activity with receptor binding remain unanswered. Evidence has accumulated that steroid hormones can exert non-classical action that is characterized by rapid effect of short duration. In most of these cases, the hormone effect occurs at the membrane level and is not associated with entry into the cell. The possible mechanisms for these non-classical actions are: (a) changes in membrane fluidity; (b) steroid hormone acting on receptors on plasma membranes; (c) steroid hormones regulating GABA(A) receptors on plasma membranes; and (d) activation of steroid receptors by factors such as EGF, IGF-1 and dopamine. Data have also been obtained indicating that receptor-mediated insertion of steroid hormones into DNA may take place with the steroid acting as a transcription factor. These new proposed mechanisms of action of steroid hormones should not be viewed as a challenge to the classical mechanism. These diverse modes of action provide for an integrated action of hormones which may be rapid and of short duration or prolonged to address the physiological needs of the individual.
引用
收藏
页码:113 / 133
页数:21
相关论文
共 195 条
[51]  
Gorski J, 1968, Recent Prog Horm Res, V24, P45
[52]   ACTIVATION, TRANSFORMATION, AND SUBUNIT STRUCTURE OF STEROID-HORMONE RECEPTORS [J].
GRODY, WW ;
SCHRADER, WT ;
OMALLEY, BW .
ENDOCRINE REVIEWS, 1982, 3 (02) :141-163
[54]   UPTAKE AND SUBCELLULAR DISTRIBUTION OF C14-LABELED STEROID IN RAT VENTRAL PROSTATE FOLLOWING IN VIVO ADMINISTRATION OF TESTOSTERONE-4-C14 [J].
HARDING, BW ;
SAMUELS, LT .
ENDOCRINOLOGY, 1962, 70 (01) :109-&
[55]   ESTROGEN-DEPENDENT AND ESTROGEN-INDEPENDENT EFFECTS OF PROGESTERONE ON THE ELECTROPHYSIOLOGICAL EXCITABILITY OF DORSAL MIDBRAIN NEURONS IN GOLDEN-HAMSTERS [J].
HAVENS, MD ;
ROSE, JD .
NEUROENDOCRINOLOGY, 1988, 48 (02) :120-129
[56]   STEREOCHEMICAL COMPLEMENTARITY OF PROGESTERONE AND CAVITIES BETWEEN BASE-PAIRS IN PARTIALLY UNWOUND DOUBLE-STRANDED DNA USING COMPUTER MODELING AND ENERGY CALCULATIONS TO DETERMINE DEGREE OF FIT [J].
HENDRY, LB ;
MAHESH, VB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 39 (02) :133-146
[57]   DRUG DESIGN WITH A NEW-TYPE OF MOLECULAR MODELING BASED ON STEREOCHEMICAL COMPLEMENTARITY TO GENE STRUCTURE [J].
HENDRY, LB .
JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 33 (12) :1173-1187
[58]   STEREOCHEMICAL COMPLEMENTARITY OF PROGESTERONE, RU486 AND CAVITIES BETWEEN BASE-PAIRS IN PARTIALLY UNWOUND DOUBLE-STRANDED DNA ASSESSED BY COMPUTER MODELING AND ENERGY CALCULATIONS [J].
HENDRY, LB ;
MAHESH, VB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 41 (3-8) :647-651
[59]   THE METABOLIC PATHWAYS FOR HOMONAL STEROIDS APPEAR TO BE REFLECTED IN THE STEREOCHEMISTRY OF DNA [J].
HENDRY, LB ;
MULDOON, TG ;
MAHESH, VB .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 42 (07) :659-670
[60]  
HENDRY LB, 1977, PERSPECT BIOL MED, V21, P120