Antinematodal agent used mainly for livestock.
A depolarizing neuromuscular-blocking agent, that causes persistent nicotinic activation resulting in spastic paralysis of susceptible nematodes. It is a drug of second-choice after benzimidazoles for treatment of ascariasis, hookworm, and pinworm infections, being effective after a single dose. (From Smith and Reynard, Textbook of Pharmacology, 1992, p920)
A species of parasitic nematode usually found in domestic pigs and a few other animals. Human infection can also occur, presumably as result of handling pig manure, and can lead to intestinal obstruction.
Agents destructive to parasitic worms. They are used therapeutically in the treatment of HELMINTHIASIS in man and animal.

Activation of single nicotinic receptor channels from Caenorhabditis elegans muscle. (1/8)

Nicotinic acetylcholine receptors (nAChRs) are pentameric neurotransmitter-gated ion channels that mediate synaptic transmission throughout the nervous system in vertebrates and invertebrates. Caenorhabditis elegans is a nonmammalian model for the study of the nervous system and a model of parasitic nematodes. Nematode muscle nAChRs are of considerable interest because they are targets for anthelmintic drugs. We show single-channel activity of C. elegans muscle nAChRs for the first time. Our results reveal that in the L1 larval stage acetylcholine (ACh) activates mainly a levamisole-sensitive nAChR (L-AChR). A single population of 39 pS channels, which are 5-fold more sensitive to levamisole than ACh, is detected. In contrast to mammalian nAChRs, open durations are longer for levamisole than for ACh. Studies in mutant strains reveal that UNC-38, UNC-63, and UNC-29 subunits are assembled into a single L-AChR in the L1 stage and that these subunits are irreplaceable, suggesting that they are vital for receptor function throughout development. Recordings from a strain mutated in the LEV-1 subunit show a main population of channels with lower conductance (26 pS), prolonged open durations, and reduced sensitivity to levamisole. Thus, although LEV-1 is preferentially incorporated into native L-AChRs, receptors lacking this subunit can still function. No single-channel activity from levamisole-insensitive nAChRs is detected. Thus, during neuromuscular transmission in C. elegans, the majority of ACh-activated current flows through L-AChRs. This study contributes to the understanding of the molecular mechanisms underlying functional diversity of the nAChR family and offers an excellent strategy to test novel antiparasitic drugs.  (+info)

Morantel allosterically enhances channel gating of neuronal nicotinic acetylcholine alpha 3 beta 2 receptors. (2/8)

 (+info)

Glutamine 57 at the complementary binding site face is a key determinant of morantel selectivity for {alpha}7 nicotinic receptors. (3/8)

 (+info)

The positive allosteric modulator morantel binds at noncanonical subunit interfaces of neuronal nicotinic acetylcholine receptors. (4/8)

 (+info)

Specificity determinants of allosteric modulation in the neuronal nicotinic acetylcholine receptor: a fine line between inhibition and potentiation. (5/8)

 (+info)

Effect of an anthelmintic program with morantel tartrate on the performance of beef cattle. (6/8)

A field trial was conducted to determine (1) the effectiveness of an anthelmintic program using morantel tartrate (MT) to control subclinical gastrointestinal parasitism among cattle on pasture and (2) the effects of the program on the performance of cattle. Two Hereford herds, each on a separate pasture with forage of comparable quality and quantity, were used. A stocking rate of .62 ha/cow-calf was maintained in both pastures. One herd consisted of 124 cows and 122 calves and served as a non-mediated control group. The second herd consisted of 126 cows and 124 calves. Cows and calves from the latter group were treated with a bolus formulation of MT at a dosage of 10 mg/kg body weight at the beginning of the trial and again 55 d later. Calves were treated again 42 d after the second treatment. Cattle were weighed individually each month and rectal fecal samples for nematode egg counts were obtained from 36 cows and 36 calves from each group at that time. These donor cattle were selected at random at the time of the first weighing; fecal samples were then obtained from the same animals throughout the study. Eggs of the Cooperia-Ostertagia-Trichostrongylus complex predominated in all fecal samplings. There was no difference in the number of nematode eggs from the two groups of cows. However, the medicated cows gained significantly more weight than the controls and had an average weight gain advantage of 28.8 kg. The medicated calves had significantly lower average egg counts and made higher weight gains than the unmedicated calves. The medicated calves had an average weight gain advantage over the control group of 11.1 kg.  (+info)

Milk production effect of a morantel tartrate treatment at calving in dairy cows with subclinical parasitism. (7/8)

A field trial involving 217 dairy cows from 13 herds located in four different areas of Quebec was conducted to determine the level of subclinical parasitism. The effect on milk production was evaluated on 116 cows following a single anthelmintic treatment with morantel tartrate administered at freshening. The results showed that this treatment increased milk production in nine herds, which was statistically significant at P 0.05).  (+info)

Activation and cooperative multi-ion block of single nicotinic-acetylcholine channel currents of Ascaris muscle by the tetrahydropyrimidine anthelmintic, morantel. (8/8)

1. We have investigated activation and block, by the tetrahydropyrimidine anthelmintic, morantel, of nicotinic-acetylcholine receptor (AChR) currents in membrane vesicles isolated from somatic muscle cells of the nematode parasite Ascaris suum. Standard single-channel recording techniques were employed. Morantel in the pipette (6 nM to 600 microM), activated single nicotinic AChR currents. 2. Kinetic properties of the main-conductance state of morantel-activated currents were investigated in detail throughout the concentration range, 0.6 microM to 600 microM. Open-time distributions were best fitted by a single exponential. Mean open-times were slightly voltage-dependent, increasing from 0.9 ms at +75 mV to 1.74 ms at -75 mV in the presence of 0.6 microM morantel. At low concentrations, closed-time distributions were best fitted by the sum of two or three exponential components. 3. As the concentration of morantel was increased (100-600 microM), fast-flickering open channel-block was observed at positive potentials, even though morantel, a cation, was only present at the extracellular surface of the membrane. The block rate was dependent on morantel concentration and both block rate and duration of block increased as the potential became less positive. A simple channel-block mechanism did not explain properties of this block. 4. At negative potentials, as the morantel concentration increased, a complex block was observed. With increases in morantel concentration two additional gap components appeared in closed-time distributions: one was short with a duration (approximately 13 ms) independent of morantel concentration; the other was long with a duration that increased with morantel concentration (up to many minutes). In combination, these two components produced a marked reduction in probability of channel opening (Po) with increasing morantel concentration. The relationship between the degrees of block and morantel concentration had a Hill coefficient of 1.6, suggesting the involvement of at least two blocking molecules. The data were analysed by use of a simple sequential double block kinetic model.  (+info)

Morantel is an anthelmintic (a medication used to treat infections caused by parasitic worms) that belongs to the class of drugs called tetrahydropyrimidines. It works by paralyzing the worms, which are then expelled from the body. Morantel is commonly used to treat roundworm and stomach worm infections in animals, particularly in swine and cattle.

It's important to note that morantel is not approved for use in humans and should only be administered under the supervision of a veterinarian to animals.

Pyrantel is an anthelmintic medication used to treat and prevent gastrointestinal parasitic infections caused by roundworms, hookworms, and pinworms in humans and animals. It works by paralyzing the parasites, allowing them to be expelled from the body. Pyrantel is available in various formulations, including tablets, suspensions, and pastes, for human and veterinary use. Common brand names include Pin-X, Reese's Pinworm Medicine, and Strongid.

'Ascaris suum' is a species of roundworm that primarily infects pigs, although it can also rarely infect humans. It is a type of parasitic nematode that lives in the intestines of its host and obtains nutrients from ingested food. The adult female worm can grow up to 40 cm in length and produces thousands of eggs every day. These eggs are passed in the feces of infected animals and can survive in the environment for years, making them a significant source of infection for other pigs or humans who come into contact with them.

In pigs, 'Ascaris suum' infection can cause a range of symptoms, including diarrhea, vomiting, and stunted growth. In severe cases, it can lead to intestinal blockages or pneumonia. Humans who become infected with 'Ascaris suum' typically experience milder symptoms, such as abdominal pain, coughing, and wheezing. However, in rare cases, the infection can cause more serious complications, particularly if the worms migrate to other parts of the body.

Preventing 'Ascaris suum' infection involves good hygiene practices, such as washing hands thoroughly after handling animals or coming into contact with soil that may contain infected feces. It is also important to properly cook pork before eating it and to avoid consuming raw or undercooked meat. In areas where 'Ascaris suum' is common, deworming programs for pigs can help reduce the risk of infection for both animals and humans.

Anthelmintics are a type of medication used to treat infections caused by parasitic worms, also known as helminths. These medications work by either stunting the growth of the worms, paralyzing them, or killing them outright, allowing the body to expel the worms through normal bodily functions. Anthelmintics are commonly used to treat infections caused by roundworms, tapeworms, flukeworms, and hookworms. Examples of anthelmintic drugs include albendazole, mebendazole, praziquantel, and ivermectin.

  • Morantel is closely related to pyrantel. (wikipedia.org)
  • Since the 1960s, there have predominantly been three classes of broad-spectrum anthelmintic drugs used to control helminths in mammals: benzimidazole/pro-benzimidazole (such as fenbendazole and febantel), tetrahydropyrimidines/imidazothiazoles (such as pyrantel, morantel/levamisole), and macrocyclic lactones (such as ivermectin and moxidectin). (vin.com)
  • Oxantel pamoate belongs to a class of drugs called tetrahydropyrimidines that also include pyrantel and morantel. (affygility.com)
  • The 'BZ's's are often combined with Morantel or Pyrantel to reduce the level of resistant worms to treatment, and to treat tapeworm infection. (ourimbahvet.com.au)
  • Morantel, prasterone, and levamisole were tested in the S. ratti rat model using dosages of 1-100 mg/kg. (biomedcentral.com)
  • Prasterone lacked activity in vivo, while treatment with 100 mg/kg morantel and levamisole cured all rats. (biomedcentral.com)
  • Prevention: For the treatment and control of abamectin sensitive strains of internal parasites (including benzimidazole, levamisole, and morantel resistant strains) of sheep and itch mite and nasal bot of sheep. (dalgetyah.com.au)
  • Broad spectrum abamectin and morantel tartrate horse worm and bot paste. (equineperformance.com.au)
  • MECWORMA and TAPE ALLWORMER utilises a combination of two horse wormers from different classes, abamectin (macrocyclic lactone) and morantel tartrate (tetrahydropyrimidine). (iahp.com.au)
  • Abamectin and morantel tartrate are both broad spectrum anthelmintics that allow for combined treatment and control of both large and small strongyles, tapeworm, cutaneous onchocerciasis and nematodes including Habronema and Draschia spp. (iahp.com.au)
  • The purpose of this study was to determine the efficacy of an abamectin (ABA) and morantel (MOR) combination(AMMO Allwormer) for the treatment of ivermectin (IVM) and ABA resistant PE. (edu.au)
  • Morantel is an anthelmintic drug used for the removal of parasitic worms in livestock. (wikipedia.org)
  • Morantel (MRT) had the highest detection frequency (100%) in compost, suggesting its ubiquitous usage and resistance to degradation during composting. (bvsalud.org)
  • The highest detection rate (96.3%) in influents was noted for the morantel, which was a feed additive. (bvsalud.org)
  • Belot, J, Camus, E & Mishra, GS 1979, ' Essai d'efficacité du traitement à base de tartrate de morantel (Exhelm II) sur la strongylose gastro-intestinale bovine en Côte d'Ivoire ', Archives de l'Institut Pasteur de Tunis , vol. 56, pp. 91-104. (itg.be)
  • For the treatment and control of abamectin sensitive strains of internal parasites of sheep (including benzimidazole, levamisole and morantel resistant strains), nasal bot and itch mite of sheep and as an aid in the control of selenium deficiency in sheep. (covine.com.au)
  • For the treatment and control of gastrointestinal parasites including those that have single, dual or triple resistance to macrocyclic lactones (including abamectin resistant strains), benzimidazoles, imidazothiazoles (levamisole/morantel) or monepantel. (farmco.com.au)

No images available that match "morantel"