Ractopamine

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Ractopamine
Ractopamine.png
Identifiers
CAS number97825-25-7 N
PubChem56052
ChemSpider50604 YesY
MeSHRactopamine
ChEMBLCHEMBL509336 YesY
Jmol-3D imagesImage 1
Properties
Molecular formulaC18H23NO3
Molar mass301.38 g mol−1
Solubility in water4100 mg/L
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N (verify) (what is: YesY/N?)
Infobox references
 
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Ractopamine
Ractopamine.png
Identifiers
CAS number97825-25-7 N
PubChem56052
ChemSpider50604 YesY
MeSHRactopamine
ChEMBLCHEMBL509336 YesY
Jmol-3D imagesImage 1
Properties
Molecular formulaC18H23NO3
Molar mass301.38 g mol−1
Solubility in water4100 mg/L
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N (verify) (what is: YesY/N?)
Infobox references

Ractopamine is a drug used as a feed additive to promote leanness in animals raised for their meat. Pharmacologically, it is a beta-adrenergic agonist. It is the active ingredient in products known as Paylean for swine and Optaflexx for cattle, developed by Elanco Animal Health, a division of Eli Lilly and Company, for use in food animals for growth promotion.

Ractopamine has been banned in the European Union, mainland China and Russia.[1][2]

Mode of action[edit]

When used as a food additive, ractopamine added to feed can be distributed via the blood to the muscle tissues, where it will bind to specific beta receptors in the muscle cell membranes. A cascade of events will then be initiated to increase protein synthesis, which results in increased muscle fiber size. Ractopamine is known to increase the rate of weight gain, improve feed efficiency, and increase carcass leanness in finishing swine. Its use in finishing swine yields about three kilograms of additional lean pork and improves feed efficiency by 10%.[3] In steers and heifers, ractopamine use increases hot carcass weight by about 5.5 and 5.0 kg, respectively.[4][unreliable source?]

Regulation around the world[edit]

Russia and China have both banned ractopamine in beef, deeming it unfit for human consumption.[5] Twenty-seven other countries, including Japan, South Korea, Mexico, Taiwan, Canada, and the United States, have determined that meat from animals fed ractopamine is safe for human consumption.[6] In the USA, ractopamine is allowed to be used at a feed concentration of 5–20 mg/kg feed for finishing pigs and in dosages of 5–10 mg/kg feed for finishing pigs heavier than 109 kg. In Canada, ractopamine is allowed in meal or pellet feed for finishing barrows, gilts, beef cattle and heavy turkeys only. The maximum residues limit of ractopamine is 50 and 10 ppb in the USA and Japan, respectively.

In August 2012, Taiwan's legislature passed amendments to the Food Safety Act, allowing ractopamine in beef.[7]

Recently, Russia has restricted beef and pork imports to those that are certified free of the additive ractopamine.[8]

Ractopamine is not allowed in the European Union as of 2012.[9][10]

Human use and route of exposure[edit]

Ractopamine is not for use in humans for any medical purposes. The more probable route of exposure to ractopamine in humans is through the consumption of food animals which have been fed ractopamine and its residue remains.

Pharmacokinetics in humans[edit]

A study was conducted to define the pharmacological response of humans to ractopamine. A single oral dose of 40 mg of ractopamine hydrochloride was given to human volunteers. The drug was rapidly absorbed; the mean blood plasma half-life was around 4 hrs and it was not detected in plasma 24 hrs after dosing. Less than 5% of total ractopamine excreted represented the parent drug, while the urinary metabolites were monoglucuronide and monosulfate conjugates, with ractopamine monosulfate being the major metabolite present.[11]

The metabolic fate of ractopamine hydrochloride is similar in the target species (pigs and cattle), laboratory animals, and humans. Besides the pharmacology effect, ractopamine may cause intoxication effect; therefore, any consumption by humans of a meat and/or byproducts of animals that consumed ractopamine with feed for growth stimulation, may result in such clinical effects as tachycardia and other heart rate increases, tremor, headache, muscle spasm, or high arterial blood pressure.[12] The effect of ractopamine on humans is not entirely known, but consumption of products that contain ractopamine residues is not advisable to people with cardiovascular diseases.

Safety concerns[edit]

Target animal safety[edit]

Ractopamine is safe for finishing pigs heavier than 240 lb (110 kg) when administered in the diet at concentrations up to 10 ppm and fed for up to 35 days.[citation needed] However, the number of ractopamine hydrochloride–treated animals exhibiting signs of injury increased during the final drive to slaughter. Since the drug was introduced, more than 160,000 pigs taking ractopamine were reported to have suffered adverse effects, as of March 2011, according to a review of FDA records. The drug has triggered more adverse reports in pigs than any other animal drug on the market. Pigs suffered from hyperactivity, trembling, broken limbs, inability to walk and death, according to FDA reports released under a Freedom of Information Act request.(FDA)[13]

Some show sheep and goats are illegally given ractopamine to enhance muscle growth.[citation needed]

Human safety[edit]

On 6 July 2012, the Codex Alimentarius Commission approved safe limits of residual ractopamine in meats.[14] In the United States, as codified under 21 C.F.R. 556.570, the safe concentrations for total residues of ractopamine hydrochloride are: 0.25 ppm in muscle, 0.75 ppm in liver, and 1.5 ppm in kidney and fat. The acceptable daily intake for total residues of ractopamine is 1.25 micrograms ractopamine hydrochloride per kilogram of body weight per day. The human safety of meat products derived from food animals fed ractopamine has been confirmed by the Joint FAO/WHO Expert Committee on Food Additives in 2004, 2006, and 2010 and by 27 regulatory authorities from around the world.[15][16][17]

Adverse effects[edit]

Acute toxicity[edit]

Oral LD50 levels in mice and rats are 3547–2545 mg/kg body weight (male and female) and 474–365 (male and female), respectively.[18]

Genotoxicity and mutagenicity[edit]

Mutation studies in prokaryotes and eukaryotes show that ractopamine is not mutagenic. However, the results of several in vitro studies, including chromosome aberration tests in human lymphocytes, are positive. The positive genotoxic results are explained with limited evidence to be due to a secondary auto-oxidative mechanism from ractopamine-catechol-producing reactive intermediates.[which?]

Carcinogenicity[edit]

Ractopamine is not considered to be a direct carcinogen. It is not listed by IARC, NTP, ACGIH, or OSHA. The induction of benign leiomyomas (tumors of smooth muscle) in mice and rats can possibly be due to a general feature of beta-adrenergic activity of ractopamine.

Cardiovascular effects[edit]

Dose-dependent changes of heart rate and cardiac output are observed within the first hour after administration of ractopamine and gradually return to baseline values. The systolic blood pressure will also increase in a dose-dependent manner, while the diastolic pressure remains unchanged.

Musculoskeletal effects[edit]

Skeletal muscle tremor is the most common adverse effect of beta-agonists, and is more likely to be seen after oral administration than after inhalation. Tremor results from an imbalance between fast- and slow-twitch muscle groups of the extremities, and its severity varies greatly between individuals. No such effects were recorded at the NOEL determined in the toxicological studies conducted in laboratory animals given ractopamine or in the study in humans on cardiovascular effects of ractopamine.

Behavioral changes[edit]

Feelings of restlessness, apprehension, and anxiety were reported effects after the use of various beta-agonists, particularly after oral or parenteral treatment. In pilot clinical trials with ractopamine, four patients showed little evidence for central nervous system stimulation. It is unclear whether long-term treatment with these drugs results in the development of tolerance to these adverse effects.

Analytical method for residues in meat[edit]

The determinative procedure for the analysis of ractopamine residues in tissue can be performed, using liver or muscle as the target tissues, by high performance liquid chromatography with fluorescence detection. The confirmatory method include reversed-phase HPLC/electrospray ionization triple tandem quadrupole mass spectrometry. The limit of quantification of the drug using this LC/MS instrument was shown to be 1 ng/g.[19]

International controversies[edit]

Mainland China[edit]

In July 2007, officials of the People's Republic of China seized US-produced pork for containing ractopamine residues.[20] Further shipments of ractopamine-fed pork were seized in September, though this time they were Canadian in origin.[21]

Republic of China (Taiwan)[edit]

Ractopamine has been banned in Taiwan since 2006.[22] In the summer of 2007, two US shipments including ractopamine-laced pork were rejected by Taiwan's health authorities, while the Taiwan government had been considering lifting the ban on such imports.[23] This resulted in mass protests in the capital city, Taipei, by swine farmers insisting that the ban remain in place. Health Minister Hou Sheng-mou (侯勝茂) declared there would be no lifting of the ban unless related laws were amended. In August 2012, Taiwan's legislature passed amendments to the food safety act allowing ractopamine in beef.

Malaysia[edit]

According to the Malaysian Food Act 1983 and Regulations (as of 5 January 2010), ractopamine is allowed in pig muscle and fat (MRL of 10 ppb), pig liver (MRL of 40 ppb) and pig kidney (MRL of 90 ppb).[24] Ractopamine is allowed as its half-life is lower, leading to reduced residues in the food, and the dose required to affect humans is much higher than other beta agonists.[25] On 30 December 2008, the Malaysian Veterinary Services Department quarantined 10 of the 656 pig farms in Malaysia, as the livestock were found to contain the banned chemical.[26][27]

Russia[edit]

On 6 June 2011, the Russian Ministry of Agriculture notified key meat exporters in Russia of the coming prohibition on the use of ractopamine in meat exported to Russia, and the requirement of submission of compliance certificates (confirming absence of ractopamine) that accompany such exported meat.

On 7 December 2012, the above prohibition went into force, and the pork and beef export became possible only upon checks that confirm such meat is ractopamine-free.


Comparison to clenbuterol[edit]

Similar to ractopamine, clenbuterol is a growth-promoting compound belonging to the beta-agonist family. It is known to have the effect of enhancing weight gain and proportion of muscle to fat. However, clenbuterol is known to have a much longer half-life in blood than ractopamine, thus has a greater potential for bioaccumulation.

Clenbuterol is reported to induce unintended side effects on humans, such as increased heart rate, muscular tremors, headache, nausea, fever, and chills. The US FDA has concluded these side effects to be unacceptable. The use of clenbuterol in food animals has been prohibited in almost all countries, including the USA, Canada, Taiwan, and Hong Kong.

See also[edit]

References[edit]

  1. ^ Bottemiller, Helena (January 25, 2012). "Dispute over drug in feed limiting US meat exports". Bottom Line. 
  2. ^ Garina, Anastasia. "Russia throws poisonous meat back to US". Pravda.ru. Retrieved 14 December 2012. 
  3. ^ Apple JK et al. (2007). "Meta-analysis of the ractopamine response in finishing swine". Prof. Anim. Sci. 23: 179–196. 
  4. ^ Elanco Study Nos. T4V200321, T4V080342, T4V160328, T4V480326, T4V080325 & T4V200324. Projection based upon a summary of Optaflexx Post-approval Research in Heifers. October 2006. Data on file.
  5. ^ http://www.usatoday.com/story/money/business/2013/06/14/smithfield-foods-4q-profit-falls-63/2423401/
  6. ^ "The Facts about U.S. Beef and Ractopamine". American Institute in Taiwan. Retrieved 5 March 2012. 
  7. ^ http://www.taipeitimes.com/News/taiwan/archives/2012/08/02/2003539254
  8. ^ http://beefmagazine.com/foreign-trade/russian-ban-ractopamine-boosts-brazilian-exports
  9. ^ http://www.globalmeatnews.com/Industry-Markets/EU-opposes-ractopamine-limit
  10. ^ http://www.efsa.europa.eu/en/efsajournal/pub/1041.htm
  11. ^ RACTOPAMINE (addendum). WHO FOOD ADDITIVES SERIES: 53
  12. ^ "Safety evaluation of ractopamine EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP)". EFSA Journal. 7 April 2009. doi:10.2903/j.efsa.2009.1041. Retrieved 2013-03-21. 
  13. ^ "Dispute Over Drug in Feed Limiting US Meat Exports". The Fern. January 25, 2012. 
  14. ^ http://www.fao.org/news/story/en/item/150953/icode/
  15. ^ Evaluation of Certain Veterinary Drug Residues in Food (Sixty-second report of the Joint FAO/WHO Expert Committee on Food Additives). WHO Technical Report Series. No. 925, 2004.
  16. ^ Evaluation of Certain Veterinary Drug Residues in Animals and Foods (Sixty-sixth report of the Joint FAO/WHO Expert Committee on Food Additives). WHO Technical Report Series. No. 939, 2006.
  17. ^ Residue Evaluation of Certain Veterinary Drugs. Joint FAO/WHO Expert Committee on Food Additives. FAO JECFA Monographs 9. 2010.
  18. ^ Safety evaluation of ractopamine. 2009. p. 10. 
  19. ^ Sakai T et al. (2007). "Determination method for ractopamine in swine and cattle tissues using LC/MS". Shokuhin Eiseigaku Zasshi 48 (5): 144–147. doi:10.3358/shokueishi.48.144. PMID 18027547. 
  20. ^ "China fights back, goes after U.S. meat", USA Today, July 14, 2007.
  21. ^ "China stops imports from Canadian pork plant over banned additive", Canada Press (2007-09-19)[dead link]
  22. ^ Lin, Hermia (August 22, 2007). "Swine farmers get rowdy over ractopamine issue". Taiwan News. Retrieved January 25, 2012. [dead link]
  23. ^ "Taiwanese farmers urge continuation of US pork import ban". Associated Press. August 21, 2007. Archived from the original on January 25, 2012. 
  24. ^ Fifteenth A Schedule, Table 1, Maximum Permitted Proportion of Drug Residues in Food.
  25. ^ "Beta-agonists hog the limelight". The Star. November 5, 2006. Retrieved January 25, 2012. 
  26. ^ "Vet Dept seals 10 pig farms". The Star. December 31, 2008. Retrieved January 25, 2012. 
  27. ^ "10 pig farms under quarantine". The Star. December 30, 2008. Archived from the original on January 25, 2012. 

External links[edit]