From toxicological problem to therapeutic use: The discovery of the mode of action of 2‐(2‐nitro‐4‐trifluoromethylbenzoyl)‐1,3‐cyclohexanedione (NTBC), its toxicology and development as a drug

NTBC is a triketone with herbicidal activity that has been shown to have a novel mode of action by inhibiting the enzyme 4‐hydroxyphenylpyruvate dioxygenase in plants. Early studies on the toxicity of this compound found that rats treated with NTBC developed corneal lesions. Investigations aimed at...

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Veröffentlicht in:Journal of inherited metabolic disease 1998-08, Vol.21 (5), p.498-506
Hauptverfasser: Lock, E. A., Ellis, M. K., Gaskin, P., Robinson, M., Auton, T. R., Provan, W. M., Smith, L. L., Prisbylla, M. P., Mutter, L. C., Lee, D. L.
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container_end_page 506
container_issue 5
container_start_page 498
container_title Journal of inherited metabolic disease
container_volume 21
creator Lock, E. A.
Ellis, M. K.
Gaskin, P.
Robinson, M.
Auton, T. R.
Provan, W. M.
Smith, L. L.
Prisbylla, M. P.
Mutter, L. C.
Lee, D. L.
description NTBC is a triketone with herbicidal activity that has been shown to have a novel mode of action by inhibiting the enzyme 4‐hydroxyphenylpyruvate dioxygenase in plants. Early studies on the toxicity of this compound found that rats treated with NTBC developed corneal lesions. Investigations aimed at understanding the mechanistic basis for the ocular toxicity discovered that the rats developed tyrosinaemia and excreted large amounts of 4‐hydroxyphenylpyruvate and 4‐hydroxyphenyllactate, owing to inhibition of the hepatic enzyme 4‐hydroxyphenylpyruvate dioxygenase. The corneal lesions resemble those seen when rats are fed a diet supplemented with tyrosine, leading us to conclude that the ocular toxicity seen with NTBC is a consequence of a marked and sustained tyrosinaemia. Studies in collaboration with Professor Sven Lindstedt showed that NTBC was a potent inhibitor of purified human liver 4‐hydroxyphenylpyruvate dioxygenase. This interaction lead to the concept of using NTBC to treat patients with tyrosinaemia type 1, to block or reduce the formation of toxic metabolites such as succinylacetoacetate in the liver. Zeneca Agrochemicals and Zeneca Pharmaceuticals made NTBC available for clinical use and, with the approval of the Swedish Medical Products Agency, a seriously ill child with an acute form of tyrosinaemia type 1 was successfully treated in February 1991. Subsequently, other children with this inborn error of metabolism in Sweden and other countries have been treated with NTBC. The drug is now available to those in need via Swedish Orphan AB.
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A. ; Ellis, M. K. ; Gaskin, P. ; Robinson, M. ; Auton, T. R. ; Provan, W. M. ; Smith, L. L. ; Prisbylla, M. P. ; Mutter, L. C. ; Lee, D. L.</creator><creatorcontrib>Lock, E. A. ; Ellis, M. K. ; Gaskin, P. ; Robinson, M. ; Auton, T. R. ; Provan, W. M. ; Smith, L. L. ; Prisbylla, M. P. ; Mutter, L. C. ; Lee, D. L.</creatorcontrib><description>NTBC is a triketone with herbicidal activity that has been shown to have a novel mode of action by inhibiting the enzyme 4‐hydroxyphenylpyruvate dioxygenase in plants. Early studies on the toxicity of this compound found that rats treated with NTBC developed corneal lesions. Investigations aimed at understanding the mechanistic basis for the ocular toxicity discovered that the rats developed tyrosinaemia and excreted large amounts of 4‐hydroxyphenylpyruvate and 4‐hydroxyphenyllactate, owing to inhibition of the hepatic enzyme 4‐hydroxyphenylpyruvate dioxygenase. The corneal lesions resemble those seen when rats are fed a diet supplemented with tyrosine, leading us to conclude that the ocular toxicity seen with NTBC is a consequence of a marked and sustained tyrosinaemia. Studies in collaboration with Professor Sven Lindstedt showed that NTBC was a potent inhibitor of purified human liver 4‐hydroxyphenylpyruvate dioxygenase. This interaction lead to the concept of using NTBC to treat patients with tyrosinaemia type 1, to block or reduce the formation of toxic metabolites such as succinylacetoacetate in the liver. Zeneca Agrochemicals and Zeneca Pharmaceuticals made NTBC available for clinical use and, with the approval of the Swedish Medical Products Agency, a seriously ill child with an acute form of tyrosinaemia type 1 was successfully treated in February 1991. Subsequently, other children with this inborn error of metabolism in Sweden and other countries have been treated with NTBC. 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Vitamins ; Herbicides - pharmacology ; Herbicides - therapeutic use ; Herbicides - toxicity ; Humans ; Medical sciences ; Metabolic diseases ; Nitrobenzoates - pharmacology ; Nitrobenzoates - therapeutic use ; Nitrobenzoates - toxicity ; Pharmacology. 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A.</creatorcontrib><creatorcontrib>Ellis, M. K.</creatorcontrib><creatorcontrib>Gaskin, P.</creatorcontrib><creatorcontrib>Robinson, M.</creatorcontrib><creatorcontrib>Auton, T. R.</creatorcontrib><creatorcontrib>Provan, W. M.</creatorcontrib><creatorcontrib>Smith, L. L.</creatorcontrib><creatorcontrib>Prisbylla, M. P.</creatorcontrib><creatorcontrib>Mutter, L. C.</creatorcontrib><creatorcontrib>Lee, D. L.</creatorcontrib><title>From toxicological problem to therapeutic use: The discovery of the mode of action of 2‐(2‐nitro‐4‐trifluoromethylbenzoyl)‐1,3‐cyclohexanedione (NTBC), its toxicology and development as a drug</title><title>Journal of inherited metabolic disease</title><addtitle>J Inherit Metab Dis</addtitle><description>NTBC is a triketone with herbicidal activity that has been shown to have a novel mode of action by inhibiting the enzyme 4‐hydroxyphenylpyruvate dioxygenase in plants. Early studies on the toxicity of this compound found that rats treated with NTBC developed corneal lesions. Investigations aimed at understanding the mechanistic basis for the ocular toxicity discovered that the rats developed tyrosinaemia and excreted large amounts of 4‐hydroxyphenylpyruvate and 4‐hydroxyphenyllactate, owing to inhibition of the hepatic enzyme 4‐hydroxyphenylpyruvate dioxygenase. The corneal lesions resemble those seen when rats are fed a diet supplemented with tyrosine, leading us to conclude that the ocular toxicity seen with NTBC is a consequence of a marked and sustained tyrosinaemia. Studies in collaboration with Professor Sven Lindstedt showed that NTBC was a potent inhibitor of purified human liver 4‐hydroxyphenylpyruvate dioxygenase. This interaction lead to the concept of using NTBC to treat patients with tyrosinaemia type 1, to block or reduce the formation of toxic metabolites such as succinylacetoacetate in the liver. Zeneca Agrochemicals and Zeneca Pharmaceuticals made NTBC available for clinical use and, with the approval of the Swedish Medical Products Agency, a seriously ill child with an acute form of tyrosinaemia type 1 was successfully treated in February 1991. Subsequently, other children with this inborn error of metabolism in Sweden and other countries have been treated with NTBC. The drug is now available to those in need via Swedish Orphan AB.</description><subject>4-Hydroxyphenylpyruvate Dioxygenase - antagonists &amp; inhibitors</subject><subject>Amino Acid Metabolism, Inborn Errors - drug therapy</subject><subject>Aminoacid disorders</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cyclohexanones - pharmacology</subject><subject>Cyclohexanones - therapeutic use</subject><subject>Cyclohexanones - toxicity</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Enzyme Inhibitors - therapeutic use</subject><subject>Enzyme Inhibitors - toxicity</subject><subject>Errors of metabolism</subject><subject>General and cellular metabolism. Vitamins</subject><subject>Herbicides - pharmacology</subject><subject>Herbicides - therapeutic use</subject><subject>Herbicides - toxicity</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Nitrobenzoates - pharmacology</subject><subject>Nitrobenzoates - therapeutic use</subject><subject>Nitrobenzoates - toxicity</subject><subject>Pharmacology. 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Vitamins</topic><topic>Herbicides - pharmacology</topic><topic>Herbicides - therapeutic use</topic><topic>Herbicides - toxicity</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Nitrobenzoates - pharmacology</topic><topic>Nitrobenzoates - therapeutic use</topic><topic>Nitrobenzoates - toxicity</topic><topic>Pharmacology. Drug treatments</topic><topic>Tyrosine - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lock, E. A.</creatorcontrib><creatorcontrib>Ellis, M. K.</creatorcontrib><creatorcontrib>Gaskin, P.</creatorcontrib><creatorcontrib>Robinson, M.</creatorcontrib><creatorcontrib>Auton, T. R.</creatorcontrib><creatorcontrib>Provan, W. M.</creatorcontrib><creatorcontrib>Smith, L. L.</creatorcontrib><creatorcontrib>Prisbylla, M. P.</creatorcontrib><creatorcontrib>Mutter, L. C.</creatorcontrib><creatorcontrib>Lee, D. 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L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>From toxicological problem to therapeutic use: The discovery of the mode of action of 2‐(2‐nitro‐4‐trifluoromethylbenzoyl)‐1,3‐cyclohexanedione (NTBC), its toxicology and development as a drug</atitle><jtitle>Journal of inherited metabolic disease</jtitle><addtitle>J Inherit Metab Dis</addtitle><date>1998-08</date><risdate>1998</risdate><volume>21</volume><issue>5</issue><spage>498</spage><epage>506</epage><pages>498-506</pages><issn>0141-8955</issn><eissn>1573-2665</eissn><coden>JIMDDP</coden><abstract>NTBC is a triketone with herbicidal activity that has been shown to have a novel mode of action by inhibiting the enzyme 4‐hydroxyphenylpyruvate dioxygenase in plants. Early studies on the toxicity of this compound found that rats treated with NTBC developed corneal lesions. Investigations aimed at understanding the mechanistic basis for the ocular toxicity discovered that the rats developed tyrosinaemia and excreted large amounts of 4‐hydroxyphenylpyruvate and 4‐hydroxyphenyllactate, owing to inhibition of the hepatic enzyme 4‐hydroxyphenylpyruvate dioxygenase. The corneal lesions resemble those seen when rats are fed a diet supplemented with tyrosine, leading us to conclude that the ocular toxicity seen with NTBC is a consequence of a marked and sustained tyrosinaemia. Studies in collaboration with Professor Sven Lindstedt showed that NTBC was a potent inhibitor of purified human liver 4‐hydroxyphenylpyruvate dioxygenase. This interaction lead to the concept of using NTBC to treat patients with tyrosinaemia type 1, to block or reduce the formation of toxic metabolites such as succinylacetoacetate in the liver. Zeneca Agrochemicals and Zeneca Pharmaceuticals made NTBC available for clinical use and, with the approval of the Swedish Medical Products Agency, a seriously ill child with an acute form of tyrosinaemia type 1 was successfully treated in February 1991. Subsequently, other children with this inborn error of metabolism in Sweden and other countries have been treated with NTBC. The drug is now available to those in need via Swedish Orphan AB.</abstract><cop>Dordrecht</cop><pub>Kluwer Academic Publishers</pub><pmid>9728330</pmid><doi>10.1023/A:1005458703363</doi><tpages>9</tpages></addata></record>
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subjects 4-Hydroxyphenylpyruvate Dioxygenase - antagonists & inhibitors
Amino Acid Metabolism, Inborn Errors - drug therapy
Aminoacid disorders
Animals
Biological and medical sciences
Cyclohexanones - pharmacology
Cyclohexanones - therapeutic use
Cyclohexanones - toxicity
Enzyme Inhibitors - pharmacology
Enzyme Inhibitors - therapeutic use
Enzyme Inhibitors - toxicity
Errors of metabolism
General and cellular metabolism. Vitamins
Herbicides - pharmacology
Herbicides - therapeutic use
Herbicides - toxicity
Humans
Medical sciences
Metabolic diseases
Nitrobenzoates - pharmacology
Nitrobenzoates - therapeutic use
Nitrobenzoates - toxicity
Pharmacology. Drug treatments
Tyrosine - metabolism
title From toxicological problem to therapeutic use: The discovery of the mode of action of 2‐(2‐nitro‐4‐trifluoromethylbenzoyl)‐1,3‐cyclohexanedione (NTBC), its toxicology and development as a drug
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