A steroid is a organic compound, either natural or man-made, which has four cycloalkane rings in its structure. Plants, animals and fungi make hundreds of different natural steroids.[1]

Steroid hormones are steroids which act as hormones in the body. Natural steroid hormones are usually made from cholesterol in the adrenal glands and gonads. Cholesterol is a plentiful steroid in animal cells: it is important for cell membranes.

Examples of steroid hormones include

One review noted: The adrenal gland hormones play a vital role in adapting to "ever-changing environmental and emergency situations, and help vertebrates in their successful survival".[2]

Prednisone is an important man-made steroid medication, used to treat inflammation.

Distribution in living things

Medical use

Some steroid hormones are anabolic steroids (AAS). Since the discovery and synthesis of testosterone in the 1930s, AAS have been used by physicians for many purposes, with varying degrees of success:

Abuse

Certain anabolic steroids, such as testosterone, are used to help make muscles stronger. Such steroids are used to improve a person's performance, but they are sometimes overused and abused by athletes. The rate of steroid abuse grew greatly in the early 21st century, all over the world. Overuse of anabolic steroids can have bad effects on the human body. They can cripple or kill. Sports organisations now regulate their use.

Biosynthesis and metabolism

Chemical-diagram flow chart
Simplification of the end of the steroid synthesis pathway, where the intermediates isopentenyl pyrophosphate (PP or IPP) and dimethylallyl pyrophosphate (DMAPP) form geranyl pyrophosphate (GPP), squalene and lanosterol (the first steroid in the pathway)

Steroidogenesis

Chemical-diagram flow chart
Human steroidogenesis, with the major classes of steroid hormones, individual steroids and enzymatic pathways.[5] Changes in molecular structure from a precursor are highlighted in white.

See also: Steroidogenic enzyme

Related pages

References

  1. Lednicer D. 2011. Steroid chemistry at a glance. Hoboken: Wiley. ISBN 978-0-470-66084-3
  2. Reul J.M. et al 1990. Adv. Exp. Med. Biol. 274, 243–256.
  3. Bode H.B. & others (2003). "Steroid biosynthesis in prokaryotes: identification of myxobacterial steroids and cloning of the first bacterial 2,3(S)-oxidosqualene cyclase from the myxobacterium Stigmatella aurantiaca". Molecular Microbiology. 47 (2): 471–81. doi:10.1046/j.1365-2958.2003.03309.x. PMID 12519197. S2CID 37959511.
  4. Desmond E. & Gribaldo S. (2009). "Phylogenomics of sterol synthesis: insights into the origin, evolution, and diversity of a key eukaryotic feature". Genome Biology and Evolution. 1: 364–81. doi:10.1093/gbe/evp036. PMC 2817430. PMID 20333205.
  5. Häggström M, Richfield D (2014). "Diagram of the pathways of human steroidogenesis". WikiJournal of Medicine. 1 (1). doi:10.15347/wjm/2014.005. ISSN 2002-4436.