Streptomycin: Difference between revisions

Jump to navigation Jump to search
m (Robot: Automated text replacement (-{{SIB}} +, -{{EH}} +, -{{EJ}} +, -{{Editor Help}} +, -{{Editor Join}} +))
mNo edit summary
Line 1: Line 1:
{{drugbox
__NOTOC__
| IUPAC_name = 5-(2,4-diguanidino-<br>3,5,6-trihydroxy-cyclohexoxy)- 4-[4,5-dihydroxy-6-(hydroxymethyl)<br>-3-methylamino-tetrahydropyran-2-yl] oxy-3-hydroxy-2-methyl<br>-tetrahydrofuran-3-carbaldehyde
{{Streptomycin}}
| Image = Streptomycin.png
{{CMG}}
| CAS_number = 57-92-1
| ATC_prefix = A07
| ATC_suffix = AA04
| ATC_supplemental = {{ATC|J01|GA01}}
| PubChem = 5999
| DrugBank = APRD00412
| C=21 | H=39 | N=7 | O=12
| molecular_weight = 581.574 g/mol
| smiles =
| melting_point = 12
| width=208}}
{{SI}}


==Overview==


==Overview==
'''Streptomycin''' is an [[antibiotic]] drug, the first of a class of drugs called [[aminoglycoside]]s to be discovered, and was the first antibiotic remedy for [[tuberculosis]]. It is derived from the [[actinobacteria|actinobacterium]] ''Streptomyces griseus''.  Streptomycin stops bacterial growth by damaging cell membranes and  inhibiting protein synthesis.  Specifically, it binds to the 16S rRNA of the bacterial ribosome, interfering with the binding of formyl-methionyl-tRNA to the 30S subunit. This prevents initiation of protein synthesis.  Humans have structurally different ribosomes from bacteria, thereby allowing the selectivity of this antibiotic for bacteria. Streptomycin cannot be given orally, but must be administered by regular [[intramuscular injection]]. An adverse effect of this medicine is [[ototoxicity]]. It can result in permanent hearing loss.
'''Streptomycin''' is an [[antibiotic]] drug, the first of a class of drugs called [[aminoglycoside]]s to be discovered, and was the first antibiotic remedy for [[tuberculosis]]. It is derived from the [[actinobacteria|actinobacterium]] ''Streptomyces griseus''.  Streptomycin stops bacterial growth by damaging cell membranes and  inhibiting protein synthesis.  Specifically, it binds to the 16S rRNA of the bacterial ribosome, interfering with the binding of formyl-methionyl-tRNA to the 30S subunit. This prevents initiation of protein synthesis.  Humans have structurally different ribosomes from bacteria, thereby allowing the selectivity of this antibiotic for bacteria. Streptomycin cannot be given orally, but must be administered by regular [[intramuscular injection]]. An adverse effect of this medicine is [[ototoxicity]]. It can result in permanent hearing loss.


==History==
==Category==
 
Aminoglycoside
 
==US Brand Names==
 
STRPETOMYCIN
 
==FDA Package Insert==
 
'''  [[Streptomycin description|Description]]'''
'''| [[Streptomycin clinical pharmacology|Clinical Pharmacology]]'''
'''| [[Streptomycin microbiology|Microbiology]]'''
'''| [[Streptomycin indications and usage|Indications and Usage]]'''
'''| [[Streptomycin contraindications|Contraindications]]'''
'''| [[Streptomycin warnings and precautions|Warnings and Precautions]]'''
'''| [[Streptomycin adverse reactions|Adverse Reactions]]'''
'''| [[Streptomycin drug interactions|Drug Interactions]]'''
'''| [[Streptomycin overdosage|Overdosage]]'''
'''| [[Streptomycin clinical studies|Clinical Studies]]'''
'''| [[Streptomycin dosage and administration|Dosage and Administration]]'''
'''| [[Streptomycin how supplied|How Supplied]]'''
'''| [[Streptomycin labels and packages|Labels and Packages]]'''
 
==Mechanism of Action==
 
==Historical Perspective==
It was first isolated on October 19, 1943 by Albert Schatz, a graduate student, in the laboratory of [[Selman Abraham Waksman]] at Rutgers University.  Waksman and his laboratory discovered several antibiotics, including [[actinomycin]], clavacin, streptothricin, streptomycin, grisein, [[neomycin]], fradicin, [[candicidin]] and candidin.  Of these, streptomycin and neomycin found extensive application in the treatment of numerous infectious diseases. Streptomycin was the first [[antibiotic]] that could be used to cure the disease [[tuberculosis]]; early production of the drug was dominated by [[Merck & Co.]] under [[George W. Merck]].
It was first isolated on October 19, 1943 by Albert Schatz, a graduate student, in the laboratory of [[Selman Abraham Waksman]] at Rutgers University.  Waksman and his laboratory discovered several antibiotics, including [[actinomycin]], clavacin, streptothricin, streptomycin, grisein, [[neomycin]], fradicin, [[candicidin]] and candidin.  Of these, streptomycin and neomycin found extensive application in the treatment of numerous infectious diseases. Streptomycin was the first [[antibiotic]] that could be used to cure the disease [[tuberculosis]]; early production of the drug was dominated by [[Merck & Co.]] under [[George W. Merck]].


The first [[randomized controlled trial]] to be completed and, therefore, the first to be published, it was run by England's Medical Research Council and pitted streptomycin and bed rest against bed rest alone, which was then the standard TB therapy. It accrued its first patients in January 1947.
The first [[randomized controlled trial]] to be completed and, therefore, the first to be published, it was run by England's Medical Research Council and pitted streptomycin and bed rest against bed rest alone, which was then the standard TB therapy. It accrued its first patients in January 1947.


== Uses ==
 
==Uses==
 
===Treatment of disease===
===Treatment of disease===


Line 41: Line 57:
ornamental crops, and controls algae in ornamental ponds and aquaria. A major use is in the control of fireblight on apple and pear trees. As in medical applications, extensive use can be associated with the development of resistant strains.
ornamental crops, and controls algae in ornamental ponds and aquaria. A major use is in the control of fireblight on apple and pear trees. As in medical applications, extensive use can be associated with the development of resistant strains.


==See also==
*[[Neomycin]]
*[[Philip D'Arcy Hart]]
== References ==
*Hurt, J. A., S. A. Thibodeau, A. S. Hirsh, C. O. Pabo and J. K. Joung (2003). "Highly specific zinc finger proteins obtained by directed domain shuffling and cell-based selection." Proc Natl Acad Sci U S A 100(21): 12271-6.
*Joung, J. K., E. I. Ramm and C. O. Pabo (2000). "A bacterial two-hybrid selection system for studying protein-DNA and protein-protein interactions." Proc Natl Acad Sci U S A 97(13): 7382-7.
*Kingston, William (2004). [http://jhmas.oxfordjournals.org/cgi/content/abstract/59/3/441 Streptomycin, Schatz v. Waksman, and the Balance of Credit for Discovery]. ''Journal of the History of Medicine and Allied Sciences'' 59 (3), 441-462.
*Mistiaen, Veronique. [http://www.guardian.co.uk/weekend/story/0,3605,823114,00.html Time, and the great healer]. The Guardian, Saturday 2 November 2002. The history behind the discovery of streptomycin.
*Lawrence, Peter A. (2002). [http://www.nature.com/cgi-taf/DynaPage.taf?file=/nature/journal/v415/n6874/full/415835a_fs.html The misallocation of credit is endemic in science]. ''[[Nature (journal)|Nature]]'' 415 (6874), 835-836.
*[http://www.epa.gov/oppsrrd1/REDs/factsheets/0169fact.pdf EPA R.E.D. Facts sheet] on use of streptomycin as a pesticide.
{{Antidiarrheals, intestinal anti-inflammatory/anti-infective agents}}
{{AminoglycosideAntiBiotics}}
[[Category:Aminoglycoside antibiotics]]
[[Category:Tuberculosis]]


==References==
{{Reflist|2}}


{{WH}}
[[Category:Antibiotics]]
{{WS}}
[[Category:Wikinfect]]

Revision as of 17:25, 6 January 2014

Streptomycin
STREPTOMYCIN® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Dosage and Administration
How Supplied
Labels and Packages

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Streptomycin is an antibiotic drug, the first of a class of drugs called aminoglycosides to be discovered, and was the first antibiotic remedy for tuberculosis. It is derived from the actinobacterium Streptomyces griseus. Streptomycin stops bacterial growth by damaging cell membranes and inhibiting protein synthesis. Specifically, it binds to the 16S rRNA of the bacterial ribosome, interfering with the binding of formyl-methionyl-tRNA to the 30S subunit. This prevents initiation of protein synthesis. Humans have structurally different ribosomes from bacteria, thereby allowing the selectivity of this antibiotic for bacteria. Streptomycin cannot be given orally, but must be administered by regular intramuscular injection. An adverse effect of this medicine is ototoxicity. It can result in permanent hearing loss.

Category

Aminoglycoside

US Brand Names

STRPETOMYCIN

FDA Package Insert

Description | Clinical Pharmacology | Microbiology | Indications and Usage | Contraindications | Warnings and Precautions | Adverse Reactions | Drug Interactions | Overdosage | Clinical Studies | Dosage and Administration | How Supplied | Labels and Packages

Mechanism of Action

Historical Perspective

It was first isolated on October 19, 1943 by Albert Schatz, a graduate student, in the laboratory of Selman Abraham Waksman at Rutgers University. Waksman and his laboratory discovered several antibiotics, including actinomycin, clavacin, streptothricin, streptomycin, grisein, neomycin, fradicin, candicidin and candidin. Of these, streptomycin and neomycin found extensive application in the treatment of numerous infectious diseases. Streptomycin was the first antibiotic that could be used to cure the disease tuberculosis; early production of the drug was dominated by Merck & Co. under George W. Merck.

The first randomized controlled trial to be completed and, therefore, the first to be published, it was run by England's Medical Research Council and pitted streptomycin and bed rest against bed rest alone, which was then the standard TB therapy. It accrued its first patients in January 1947.


Uses

Treatment of disease

  • In veterinary medicine, streptomycin is the first line antibiotic for use against gram negative bacteria in large animals (horses, cattle, sheep etc.). It is commonly combined with procaine penicillin for intramuscular injection.

Bacterial selection experiments

When grown on medium containing streptomycin, bacteria such as Escherichia coli are dependent upon expression of the aadA gene in order to survive (Joung et al., 2000). Thus, a suitably engineered E. coli strain, can be combined with a streptomycin-doped medium to select only bacteria hosting a successful interaction in two-hybrid screening experiments and methods derivative of two-hybrid screening (Hurt et al., 2003; Joung et al., 2000)

Pesticide

Streptomycin is also used as a pesticide, to combat the growth of bacteria, fungi, and algae. Streptomycin controls bacterial and fungal diseases of certain fruit, vegetables, seed, and ornamental crops, and controls algae in ornamental ponds and aquaria. A major use is in the control of fireblight on apple and pear trees. As in medical applications, extensive use can be associated with the development of resistant strains.


References