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|Class of antibiotics}}
{{Use dmy dates|date=October 2023}}


==Etymology==
'''Tetracycline antibiotics''' are a class of [[antibiotics]] that are used to treat a wide variety of infections. They 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==
==Structure==
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.
[[File:Tetracycline_numbering.svg|thumb|right|250px|Numbering of the tetracycline structure.]]
Tetracyclines are defined by their four hydrocarbon rings, which are fused together. The basic structure of tetracyclines allows for various modifications, leading to different derivatives with varying properties and spectrum of activity.


==Mechanism of Action==
==Mechanism of Action==
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.
Tetracyclines work by inhibiting [[protein synthesis]] in bacteria. They bind to the 30S ribosomal subunit, preventing the attachment of [[aminoacyl-tRNA]] to the [[ribosome]] and thus inhibiting the addition of new amino acids to the growing peptide chain. This action is generally bacteriostatic, meaning it inhibits the growth and reproduction of bacteria rather than killing them outright.


==Types of Tetracycline Antibiotics==
==Spectrum of Activity==
There are several types of tetracycline antibiotics, including:
Tetracyclines are broad-spectrum antibiotics, effective against a wide range of [[Gram-positive]] and [[Gram-negative]] bacteria. They are also active against certain intracellular pathogens such as ''[[Chlamydia]]'', ''[[Mycoplasma]]'', and ''[[Rickettsia]]''.


* [[Chlortetracycline]]
==Clinical Uses==
* [[Oxytetracycline]]
Tetracyclines are used to treat various infections, including:
* [[Demeclocycline]]
* [[Respiratory tract infections]]
* [[Doxycycline]]
* [[Urinary tract infections]]
* [[Minocycline]]
* [[Acne vulgaris]]
 
* [[Cholera]]
==Uses==
* [[Lyme disease]]
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]].
* [[Rocky Mountain spotted fever]]


==Side Effects==
==Side Effects==
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.
Common side effects of tetracyclines include gastrointestinal disturbances, such as nausea and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Tetracyclines can affect bone and tooth development, so they are generally avoided in children under the age of 8 and in pregnant women.


==Resistance==
==Resistance==
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.
[[Bacterial resistance]] to tetracyclines can occur through several mechanisms, including efflux pumps that expel the drug from the cell, ribosomal protection proteins that prevent tetracycline binding, and enzymatic inactivation of the drug.
 
==Derivatives==
Several derivatives of tetracycline have been developed to overcome resistance and improve pharmacokinetic properties. These include doxycycline and minocycline, which have improved absorption and longer half-lives compared to the original tetracycline.
 
==Related pages==
* [[Antibiotic resistance]]
* [[Protein synthesis inhibitors]]
* [[Streptomyces]]


[[Category:Antibiotics]]
[[Category:Antibiotics]]
[[Category:Medicine]]
[[Category:Tetracyclines]]
[[Category:Pharmacology]]
 
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Latest revision as of 14:48, 22 February 2025

Class of antibiotics



Tetracycline antibiotics are a class of antibiotics that are used to treat a wide variety of infections. They are derived from the bacterium Streptomyces and are characterized by their four-ring molecular structure.

Structure[edit]

Numbering of the tetracycline structure.

Tetracyclines are defined by their four hydrocarbon rings, which are fused together. The basic structure of tetracyclines allows for various modifications, leading to different derivatives with varying properties and spectrum of activity.

Mechanism of Action[edit]

Tetracyclines work by inhibiting protein synthesis in bacteria. They bind to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the ribosome and thus inhibiting the addition of new amino acids to the growing peptide chain. This action is generally bacteriostatic, meaning it inhibits the growth and reproduction of bacteria rather than killing them outright.

Spectrum of Activity[edit]

Tetracyclines are broad-spectrum antibiotics, effective against a wide range of Gram-positive and Gram-negative bacteria. They are also active against certain intracellular pathogens such as Chlamydia, Mycoplasma, and Rickettsia.

Clinical Uses[edit]

Tetracyclines are used to treat various infections, including:

Side Effects[edit]

Common side effects of tetracyclines include gastrointestinal disturbances, such as nausea and diarrhea. They can also cause photosensitivity, leading to an increased risk of sunburn. Tetracyclines can affect bone and tooth development, so they are generally avoided in children under the age of 8 and in pregnant women.

Resistance[edit]

Bacterial resistance to tetracyclines can occur through several mechanisms, including efflux pumps that expel the drug from the cell, ribosomal protection proteins that prevent tetracycline binding, and enzymatic inactivation of the drug.

Derivatives[edit]

Several derivatives of tetracycline have been developed to overcome resistance and improve pharmacokinetic properties. These include doxycycline and minocycline, which have improved absorption and longer half-lives compared to the original tetracycline.

Related pages[edit]