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Related Concept Videos

Internal Receptors01:31

Internal Receptors

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Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
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Progestins and androgens

M Whitehead1

  • 1King's Healthcare Trust, King's College Hospital, London, United Kingdom.

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|December 1, 1994
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Adding progestin or androgen to estrogen replacement therapy (ERT) alters its effects on arterial disease risk factors. The impact on lipids and lipoproteins is complex, with both beneficial and adverse modifications observed, necessitating further research.

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Area of Science:

  • Cardiovascular Health
  • Endocrinology
  • Pharmacology

Background:

  • Estrogen replacement therapy (ERT) has known effects on arterial disease risk.
  • The influence of combined hormone therapies on cardiovascular markers requires clarification.

Purpose of the Study:

  • To evaluate how progestin or androgen addition to ERT modifies estrogen's effects on arterial disease risk.
  • To synthesize current literature on the cardiovascular implications of combined hormone therapies.

Main Methods:

  • Literature review of population studies, clinical trials, and laboratory investigations.
  • Focus on postmenopausal women receiving exogenous progestin or androgen with estrogen.
  • Analysis of outcomes including lipids, lipoproteins, carbohydrate metabolism, and coagulation.

Main Results:

  • Progestin and androgen addition modify estrogen-induced lipid and lipoprotein changes.
  • Progestins show potentially adverse effects (lowering HDL2-C) and beneficial effects (lowering triglycerides).
  • Data on androgens suggest they may counteract estrogen's positive effects on HDL cholesterol, with overall clinical effects remaining unpredictable.

Conclusions:

  • The addition of progestins or androgens to ERT significantly alters cardiovascular risk profiles.
  • Current data are insufficient to predict the precise clinical outcomes of combined hormone therapies.
  • Further research is crucial to elucidate the complex interactions and long-term effects on arterial health.