Quinolone: Difference between revisions

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imported>Howard C. Berkowitz
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imported>Howard C. Berkowitz
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  | editor = Hardman JG, Limberd LE, Molinoff PB, Ruddon RW, Alfred Goodman Gilman
  | editor = Hardman JG, Limberd LE, Molinoff PB, Ruddon RW, Alfred Goodman Gilman
  | publisher = McGraw-Hill | year = 1996}}, pp. 1065-1068</ref>
  | publisher = McGraw-Hill | year = 1996}}, pp. 1065-1068</ref>
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* [[Cinoxacin]]
* [[Ciprofloxacin]]
* [[Enoxacin]]
* [[Gatifloxacin]] (respiratory quinolone)
* [[Gemifloxacin]]
* [[Grepafloxacin]]
* [[Levofloxacin]] (respiratory quinolone)
{{col-break|width=33%}}
* [[Lomefloxacin]]
* [[Moxifloxacin]] (respiratory quinolone
* [[Norfloxacin]]
* [[Ofloxacin]]
* [[Pefloxacin]]
* [[Sparfloxacin]]
* [[Trovafloxacin]]
{{col-break|width=33%}}
{{Image|Ciprofloxacin structure.jpg|right|250px|Ciprofloxacin, a simple fluoroquinolone}}
{{col-end}}


==Mode of action==
==Mode of action==
Quinolones inhibit the enzyme [[DNA gyrase]].
The mechanism of action for quinolones is different from that of [[macrolide]]s, beta-[[lactam]]s, [[aminoglycoside]]s, or [[tetracycline]]s, so organisisms resistant to those classes of antibiotic drugs may be susceptible to quinolones.  In particular, the quinolones interfere with [[topoisomerase]] enzymes, including [[topoisomerase II]] (DNA gyrase) and [[topoisomerase IV]], which are vital to bacterial [[DNA]] [[DNA replication|replication]], [[DNA transcription|transcription]], [[DNA repair|repair]] and [[DNA recombination|recombination]].  
==Classes==
==Classes==
===Non-fluorinated===
===Non-fluorinated===
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[[Enrofloxacin]] is marketed for veterinary use as Baytril.
[[Enrofloxacin]] is marketed for veterinary use as Baytril.
==Interactions==
==Side effects==
Because the use of fluoroquinolones may lead to [[tendinitis]] or tendon rupture, especially in the [[Achilles tendon]], the FDA requires a "black box" warning for these medications. The cause of the tendon damage is not yet determined.
==References==
==References==
<references/>
<references/>

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In medicine, quinolones are antibiotics that are "a group of derivatives of naphthyridine carboxylic acid, quinoline carboxylic acid, or nalidixic acid."[1] Nadixilic acid's effects are localized to the urinary tract, but it was the first quinolone in general use. The subsequent quinolones, with broader spectra, were fluorinated and are often called fluoroquinolones.[2]

(CC) Image: David E. Volk
Ciprofloxacin, a simple fluoroquinolone

Mode of action

The mechanism of action for quinolones is different from that of macrolides, beta-lactams, aminoglycosides, or tetracyclines, so organisisms resistant to those classes of antibiotic drugs may be susceptible to quinolones. In particular, the quinolones interfere with topoisomerase enzymes, including topoisomerase II (DNA gyrase) and topoisomerase IV, which are vital to bacterial DNA replication, transcription, repair and recombination.

Classes

Non-fluorinated

Nadixilic acid has no action beyond the urinary tract; it is not absorbed systemically.

Fluoroquinolones

The first, unspecialized systemic quinolones included ciprofloxacin, ofloxacin and norfloxacin. Of these, ciprofloxacin and levofloxacin have enhanced activity against Pseudomonas.

'Respiratory quinolones' are levofloxacin, gatifloxacin, or moxifloxacin. However, gatifloxacin can cause dysglycemia.[3]

Enrofloxacin is marketed for veterinary use as Baytril.

Interactions

Side effects

Because the use of fluoroquinolones may lead to tendinitis or tendon rupture, especially in the Achilles tendon, the FDA requires a "black box" warning for these medications. The cause of the tendon damage is not yet determined.

References

  1. Anonymous (2024), Quinolone (English). Medical Subject Headings. U.S. National Library of Medicine.
  2. Hardman JG, Limberd LE, Molinoff PB, Ruddon RW, Alfred Goodman Gilman, ed. (1996), Goodman & Gilman's The Pharmacological Basis of Therapeutics (Ninth ed.), McGraw-Hill, pp. 1065-1068
  3. Park-Wyllie LY, Juurlink DN, Kopp A, Shah BR, Stukel TA, Stumpo C et al. (2006). "Outpatient gatifloxacin therapy and dysglycemia in older adults.". N Engl J Med 354 (13): 1352-61. DOI:10.1056/NEJMoa055191. PMID 16510739. Research Blogging.