Tetracycline chemical structure
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Tetracycline

This article deals with the specific antibiotic called Tetracycline. For the group of antibiotics known as the Tetracyclines, see Category:Tetracycline_antibiotics. more...

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Tetracycline is an antibiotic produced by the streptomyces bacterium, indicated for use against many bacterial infections. It is commonly used to treat acne. It is sold under the brand names Sumycin®; Tetracyn®; Tetralysal 300®, Panmycin®, Brodspec® and Tetracap®, among others. Actisite® is a thread-like fiber form, used in dental applications. It is also used to produce several semi-synthetic derivatives, which are known as the Tetracyclines.

History

Tetracycline was first discovered by Lloyd Conover in the research departments of Pfizer. The patent for Tetracycline was first issued in 1955 (patent number 2,699,054). Tetracycline sparked the development of many chemically altered antibiotics and in doing so has proved to be one of the most important discoveries made in the field of antibiotics.

Mechanism and resistance

Tetracycline inhibits cell growth by inhibiting translation. It binds to the 30S ribosomal subunit and prevents the amino-acyl tRNA from binding to the A site of the ribosome. The binding is reversible in nature.

Cells become resistant to tetracyline by at least two mechanisms: efflux and ribosomal protection. In efflux, a resistance gene encodes a membrane protein that actively pumps tetracycline out of the cell. This is the mechanism of action of the tetracycline resistance gene on the artificial plasmid pBR322. In ribosomal protection, a resistance gene encodes a protein which binds to the ribosome and prevents tetracycline from acting on the ribosome.

Contraindications

When ingested, it is usually recommended that tetracycline should be taken on an empty stomach with a full glass of water unless upset stomach becomes a problem (please ask your doctor). This is partly due to the fact that tetracycline binds easily with magnesium, aluminium, iron, and calcium, which reduces its ability to be completely absorbed by the body. Dairy products, preparations containing iron, or large amounts of sunlight are not recommended directly after taking the drug.

Tetracycline use should be avoided during pregnancy and in the very young (less than 6 years) because it will result in permanent staining of teeth causing an unsightly cosmetic result.

Tetracyclines also become dangerous past their expiration dates. While most prescription drugs lose potency after their expiration dates, tetracyclines are known to become toxic over time; expired tetracyclines can cause serious damage to the kidneys.

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Pleurodesis with tetracycline or with talc-variables measured in terms of effectiveness
From CHEST, 10/1/05 by Sara Freitas

PURPOSE: establish the effectiveness of pleurodesis according to treatment option (tetracycline, tale slurry or thoracoscopic talc poudrage) correlating analytical parameters of pleural fluid.

METHODS: retrospective analysis over a five year period from January 2000 to December 2004 which included 71 procedures carried out in a Pulmonology department. Fifteen cases were excluded from the study for not fulfilling the required criteria.

RESULTS: Fifty-six pleurodesis were performed on 54 patients; 34 procedures the sclerosant agent used was tetracycline and in 22 talc. 47 cases the underlying cause was malignant pleural effusion, four pleural effusions of unknown aetiology, one pleural effusion due to Waldenstrom macroglobulinemia with lung involvement, one recurrent pneumothorax and 1 hydropneumothorax. Failure was indicated by evidence of recurrent pleural fluid. Pleurodesis with talc was successful in 29 of 34 (85%) and with tetracycline in 17 of 22 (77%).Analytical parameters of pleural fluid were thoroughly evaluated showing mean pH measurement of 7.56, total protein 4.24 mg/dl, glucose 95 mg/dl, LDH 922 U/L, ADA 16.2 mg/dl in successful pleurodesis with talc;mean pH measurement of 7.34,total protein 4.39 mg/dl, glucose 88.8mg/dl, LDH 734.7 U/L, ADA 15.8 mg/dl in successful pleurodesis with tatracycline; mean pH measurement of 7.73,total protein 4.39 mg/dl, glucose 88.8 mg/dl, LDH 734.7 U/L, ADA 15.8 mg/dl in successful pleurodesis with talc; mean ph 7.34, total protein 4.04 mg/dl,glucose 54.5 mg/dl, LDH 3078 U/L, ADA 9.87 mg/dl in unsuccessful pleurodesis with tetracycline; mean pH measurement of 7.52, total protein 4.9mg/dl, glucose 45.5, LDH 3078 U/L, ADA 9.87 mg/dl in unsuccessful pleurodesis with talc. Total cell count of pleural fluid, blood measurement of reactive C protein and LDH were also considered in this study.

CONCLUSION: pleurodesis with talc was more successful than with tetracycline. The comparative study of successful and unsuccessful cases with both the pleural sclerosants shows there are significant variations of pleural glucose, LDH and ADA in tale pleurodesis and pH, glucose and LDH in tetracycline pleurodesis.

CLINICAL IMPLICATIONS: Talc is the agent of choice when utilizing pleurodesis and pleural analytival parameters may be useful prognostic tools.

DISCLOSURE: Sara Freitas, None.

Sara Freitas MD * Jessica Cemlyn-Jones MD Carlos R. Cordeiro PhD Luis C. Oliveira PhD Manuel F. Baganha PhD Departamento de Ciencias Pneumologicas e Alergologicas dos HUC, Coimbra, Portugal

COPYRIGHT 2005 American College of Chest Physicians
COPYRIGHT 2005 Gale Group

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