Ractopamine
Encyclopedia
Ractopamine is a drug that is used as a feed additive to promote leanness in pigs raised for their meat. Pharmacologically, it is a beta-adrenoceptor 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 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 3 kilograms of additional lean pork and improves feed efficiency by 10%. In steers and heifers, ractopamine use increases hot carcass weight by about 5.5 kilograms and 5 kilograms, respectively.

Mode of action

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. Cascade of event will then be initiated to increase protein synthesis, which results in increase in muscle fiber size.

Metabolism

Ractopamine has been shown to be absorbed, distributed and eliminated rapidly in pigs, cattle, laboratory animals and primates. It is excreted mainly via urine and feces in the original form or its metabolites. The metabolites, which were formed by conjugation of the hydroxyl group, are identified to be monoglucuronides of ractopamine. Significant biliary excretion occurs, which is indicative of first pass metabolism. The metabolic fate of ractopamine is similar among various species.

Regulations of ractopamine around the world

Ractopamine is currently allowed to be used as growth promoters to increase lean muscle mass in pigs and cattle in around 25 countries worldwide, including USA, Canada, Korea, Mexico and Indonesia. 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, finishing beef cattle and finishing heavy turkeys (toms and hens) only. The maximum residues limit of ractopamine is 50 ppb and 10 ppb in the USA and Japan, respectively.

On the contrary, over 150 countries, including EU, China and Taiwan, have prohibited the use of ractopamine as leanness-enhancing agent. In Taiwan, shipments of beef from the USA are reported to be rejected by the health authority, due to positive result for ractopamine tested with the beef. There is still no global consensus on the safety of the feed additive

Human use and route of exposure

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

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 the volunteers. Ractopamine was rapidly absorbed. The mean half-life was around 4 h. Ractopamine was not detected in plasma 24 hrs after dosing. It was shown that <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.

Safety concerns

The Codex Alimentarius Commission has reaffirmed the human safety for Elanco’s feed ingredient compound ractopamine during its 33rd session in Geneva, Switzerland, by holding the maximum residue levels at Step 8 with a work plan. .

Target animal safety

Ractopamine is safe for finishing pigs heavier than 240 pounds when administered in the diet at concentrations up to 10 ppm and fed for up to 35 days. However, there was an increase in the number of ractopamine hydrochloride-treated animals exhibiting signs of injury during the final drive to slaughter. (FDA)

Human safety

As codified under 21 CFR 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 (JECFA) in 2004, 2006, and 2010 and by 27 regulatory authorities from around the world.

Acute toxicity

Oral in mouse and rat are 3547-2545 mg/kg bw (male and female) and 474-365 (male and female), respectively.

Genotoxicity and mutagen
Mutagen
In genetics, a mutagen is a physical or chemical agent that changes the genetic material, usually DNA, of an organism and thus increases the frequency of mutations above the natural background level. As many mutations cause cancer, mutagens are therefore also likely to be carcinogens...

icity

Mutation studies in prokaryote
Prokaryote
The prokaryotes are a group of organisms that lack a cell nucleus , or any other membrane-bound organelles. The organisms that have a cell nucleus are called eukaryotes. Most prokaryotes are unicellular, but a few such as myxobacteria have multicellular stages in their life cycles...

s and eukaryote
Eukaryote
A eukaryote is an organism whose cells contain complex structures enclosed within membranes. Eukaryotes may more formally be referred to as the taxon Eukarya or Eukaryota. The defining membrane-bound structure that sets eukaryotic cells apart from prokaryotic cells is the nucleus, or nuclear...

s show that ractopamine is non-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.

Carcinogenicity

Ractopamine is considered not to be a direct carcinogen. It is not listed by IARC
IARC
IARC may refer to:* International Aerial Robotics Competition* International Agency for Research on Cancer* International Arctic Research Center* Israel Amateur Radio Club* iArc, South Korean architecture firm...

, NTP
NTP
-Politics:* Nation Transformation Party, a political party in Papua New Guinea* National Toxicology Program, part of the United States Department of Health and Human Services* Ninh Thuan Province, a province in Vietnam...

, ACGIH, or OSHA
OSHA
OSHA may refer to:* Occupational Safety and Health Administration, a federal agency of the United States that regulates workplace safety and health...

. 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

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.

Musculo-skeletal effects

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 low-twitch muscle groups of the extremities, and its severity varies greatly between individuals. No such effects were recorded at the NOEL
Noel
Noel is a masculine French given name derived from noël . The actual feminine form is Noelle, but in English-speaking regions Noel is sometimes used for females as well...

 determined in the toxicological studies conducted in laboratory animals given ractopamine or in the study in humans on cardiovascular effects of ractopamine.

Behavioral changes

Feelings of restlessness, apprehension, and anxiety were reported side-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

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
High performance liquid chromatography
High-performance liquid chromatography , HPLC, is a chromatographic technique that can separate a mixture of compounds and is used in biochemistry and analytical chemistry to identify, quantify and purify the individual components of the mixture.HPLC typically utilizes different types of stationary...

 (HPLC) with fluorescence detection. The confirmatory method include reversed-phase HPLC/electrospray ionization triple tandem quadrupole mass spectrometry (LC/ESI-MS-MS). The limit of quantification (LOQ) of the drug using LC/MS was shown to be 1 ng/g.

People's Republic of China

In July 2007 Chinese officials seized U.S.-produced pork for containing ractopamine residues. Further shipments of ractopamine fed pork were seized in September, though this time they were Canadian in origin.

Republic of China (Taiwan)

Ractopamine has been banned in Taiwan since 2006.

In the summer of 2007, the substance caused considerable controversy in Taiwan
Taiwan
Taiwan , also known, especially in the past, as Formosa , is the largest island of the same-named island group of East Asia in the western Pacific Ocean and located off the southeastern coast of mainland China. The island forms over 99% of the current territory of the Republic of China following...

. Two U.S. 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. This resulted in mass protests in the capital of Taipei
Taipei
Taipei City is the capital of the Republic of China and the central city of the largest metropolitan area of Taiwan. Situated at the northern tip of the island, Taipei is located on the Tamsui River, and is about 25 km southwest of Keelung, its port on the Pacific Ocean...

by swine farmers insisting that the ban remain in place. Department of Health Minister Hou Sheng-mou (侯勝茂) declared that there would be no lifting of the ban unless related laws were amended.

Malaysia

According to the Malaysian Food Act 1983 and Regulations (as of 5th 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). (Fifteenth A Schedule, Table 1, Maximum Permitted Proportion of Drug Residues in Food). Ractopamine is allowed as its half-life is lower, leading to reduced residues in the food, and the dose required to affect in humans is much higher that other beta agonists. On 30 December 2008, the Malaysian Veterinary Services Department quarantined 10 out of the 656 pig farms in Malaysia, as the livestock were found to contain the banned chemical.

Comparision of ractopamine and clenbuterol

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 and 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. Its use has been prohibited in almost all countries, including the USA, Canada, Taiwan, Hong Kong. On the contrary, ractopamine is allowed to be used at the recommended concentrations in food animals for growth promotion in some countries such as the United States, Canada, Australia.

External links

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