Tetracycline antibiotics: Difference between revisions

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'''Tetracycline Antibiotics''' are a type of [[antibiotic]] that are used to treat a wide range of [[bacterial infection]]s. They are named after their four ("tetra-") hydrocarbon rings ("-cycl-") derivation ("-ine"). They are defined as a subclass of [[polyketides]].
{{Short description|A class of broad-spectrum antibiotics derived from Streptomyces bacteria}}


==Etymology==
'''Tetracycline antibiotics''' are a group of broad-spectrum antibiotics that are effective against a wide range of microorganisms, including gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, rickettsiae, and protozoan parasites. These antibiotics are derived from the bacterium ''[[Streptomyces]]'' and are characterized by their four-ring molecular structure.
The term "tetracycline" is derived from the Greek words "tetra", meaning four, and "kuklos", meaning circle or ring. This is in reference to the four hydrocarbon rings that are a part of the tetracycline structure.


==History==
==Mechanism of Action==
Tetracycline antibiotics were first discovered in the late 1940s by a team of scientists led by [[Benjamin Minge Duggar]]. The first tetracycline antibiotic, chlortetracycline, was introduced in 1948.
Tetracyclines work by inhibiting protein synthesis in bacteria. They achieve this by binding to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the ribosomal acceptor (A) site. This action effectively halts the addition of new amino acids to the nascent peptide chain, thereby inhibiting bacterial growth and reproduction.
 
==Clinical Uses==
Tetracyclines are used to treat a variety of infections, including:
* [[Acne vulgaris]]
* [[Cholera]]
* [[Brucellosis]]
* [[Plague]]
* [[Rickettsial infections]] such as [[Rocky Mountain spotted fever]]
* [[Chlamydia trachomatis]] infections
* [[Mycoplasma pneumoniae]] infections


==Mechanism of Action==
==Side Effects==
Tetracycline antibiotics work by inhibiting [[protein synthesis]] in bacteria, preventing them from growing and multiplying. They do this by binding to the 30S ribosomal subunit in the bacteria, which prevents the attachment of the aminoacyl-tRNA to the RNA-ribosome complex.
Common side effects of tetracycline antibiotics include gastrointestinal disturbances such as nausea, vomiting, and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Long-term use can result in discoloration of teeth and affect bone growth in children.


==Types of Tetracycline Antibiotics==
==Resistance==
There are several types of tetracycline antibiotics, including:
Bacterial resistance to tetracyclines can occur through several mechanisms, including:
* Efflux pumps that expel the antibiotic from the bacterial cell
* Ribosomal protection proteins that prevent tetracycline binding
* Enzymatic inactivation of the antibiotic


* [[Chlortetracycline]]
==Examples of Tetracyclines==
* [[Oxytetracycline]]
Some commonly used tetracycline antibiotics include:
* [[Demeclocycline]]
* [[Tetracycline]]
* [[Doxycycline]]
* [[Doxycycline]]
* [[Minocycline]]
* [[Minocycline]]
* [[Tigecycline]]


==Uses==
==History==
Tetracycline antibiotics are used to treat a variety of bacterial infections, including [[acne]], [[cholera]], [[pneumonia]], [[Lyme disease]], [[chlamydia]], and [[syphilis]]. They are also used in the treatment of [[malaria]] when used in combination with [[quinine]].
The first tetracycline, chlortetracycline, was discovered in the late 1940s. It was isolated from ''[[Streptomyces aureofaciens]]''. Since then, several derivatives have been developed to improve efficacy and reduce side effects.


==Side Effects==
==Images==
Common side effects of tetracycline antibiotics include nausea, vomiting, diarrhea, and skin rash. In rare cases, they can cause serious side effects such as liver damage, pancreatitis, and photosensitivity.
[[File:Tetracycline.svg|thumb|right|Chemical structure of tetracycline]]
[[File:Doxycycline.png|thumb|left|Chemical structure of doxycycline]]


==Resistance==
==Related Pages==
Bacterial resistance to tetracycline antibiotics is a growing concern. This resistance can occur through several mechanisms, including decreased uptake of the drug, increased efflux, and mutation of the 30S ribosomal subunit.
* [[Antibiotic resistance]]
* [[Protein synthesis inhibitors]]
* [[Broad-spectrum antibiotics]]


[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Medicine]]
[[Category:Tetracyclines]]
[[Category:Pharmacology]]
 
{{stub}}
== Tetracycline_antibiotics ==
<gallery>
File:Tetracycline_numbering.svg|Tetracycline numbering
File:6deoxy6demethyltetracycline.jpg|6-Deoxy-6-demethyltetracycline
</gallery>

Revision as of 17:43, 18 February 2025

A class of broad-spectrum antibiotics derived from Streptomyces bacteria


Tetracycline antibiotics are a group of broad-spectrum antibiotics that are effective against a wide range of microorganisms, including gram-positive and gram-negative bacteria, chlamydiae, mycoplasmas, rickettsiae, and protozoan parasites. These antibiotics are derived from the bacterium Streptomyces and are characterized by their four-ring molecular structure.

Mechanism of Action

Tetracyclines work by inhibiting protein synthesis in bacteria. They achieve this by binding to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the ribosomal acceptor (A) site. This action effectively halts the addition of new amino acids to the nascent peptide chain, thereby inhibiting bacterial growth and reproduction.

Clinical Uses

Tetracyclines are used to treat a variety of infections, including:

Side Effects

Common side effects of tetracycline antibiotics include gastrointestinal disturbances such as nausea, vomiting, and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Long-term use can result in discoloration of teeth and affect bone growth in children.

Resistance

Bacterial resistance to tetracyclines can occur through several mechanisms, including:

  • Efflux pumps that expel the antibiotic from the bacterial cell
  • Ribosomal protection proteins that prevent tetracycline binding
  • Enzymatic inactivation of the antibiotic

Examples of Tetracyclines

Some commonly used tetracycline antibiotics include:

History

The first tetracycline, chlortetracycline, was discovered in the late 1940s. It was isolated from Streptomyces aureofaciens. Since then, several derivatives have been developed to improve efficacy and reduce side effects.

Images

Chemical structure of tetracycline
File:Doxycycline.png
Chemical structure of doxycycline

Related Pages