0% found this document useful (0 votes)
7 views3 pages

Anticestodal Drugs

The document discusses various anticestodal drugs used to treat tapeworm infections in animals, categorizing them into natural organic compounds, inorganic compounds, and synthetic organic compounds. It highlights the mechanisms of action, clinical uses, and potential toxicities of these drugs, including Niclosamide, Praziquantel, and Epsiprantel. The document emphasizes the importance of complete parasite removal for effective treatment.

Uploaded by

erenyeager667788
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
7 views3 pages

Anticestodal Drugs

The document discusses various anticestodal drugs used to treat tapeworm infections in animals, categorizing them into natural organic compounds, inorganic compounds, and synthetic organic compounds. It highlights the mechanisms of action, clinical uses, and potential toxicities of these drugs, including Niclosamide, Praziquantel, and Epsiprantel. The document emphasizes the importance of complete parasite removal for effective treatment.

Uploaded by

erenyeager667788
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 3

01-Jun-21

Introduction
• Cestodes- true tapeworms
• Taeniacides: Anticestodal (Antitapeworms) drugs that
cause the death of the tapeworm in situ are referred to
Anticestodal Drugs as taeniacides e.g. Dichlorophen
• Taeniafuge: Compounds that cause or facilitate
tapeworm expulsion are termed taeniafuge e.g.
Arecoline HBr
Dr Mazhar Ul Haq • They interfere with the ability of the tapeworms to
Dr Asif Riaz maintain their position in the digestive tract by
mucosal attachment of the scolex & by undulation
• The administration of taeniafuge is generally
accompanied by purgation

1 2

Background Natural organic compounds


• Undulation: Action of moving smoothly up and down • Earliest drugs
• Destrobilization: Some drugs merely remove the
proglottids & soma but leave the scolex intact • Plant origin
• This is unsatisfactory in antiparasitic action • Examples include
• As cestodes scolex is capable of regeneration an entire • Pomegranate, Pumpkin seeds, Cucurbitine,
organism
Male fern extract, Arecoline, Nicotine sulfate,
• Successful antitapeworm treatment is complete
removal of the parasite Kamomela
• The usual interval from destrobilization to potency is
approx 3 weeks

3 4

Inorganic compounds Synthetic Organic Compounds


• Tin dust, Lead arsenate, CuSO4, KMnO4 • Bunamidine HCl was developed in 1960s
• For long time, lead arsenate (often mixed with • Available as tablets
Phenothiazine) was used to treat tapeworm • Requires fasting before treatment
infections in sheep • Used in cestode infection in dogs & cats
• Due to low safety margin, no longer used • Bunamidine Hydroxynaphtrate – oral
• CuSO4 drench used to control stomach worms suspension
• KMnO4 is used for the control of parasitic • Effective against Moneizia infection in small
infestations in fish ruminants
5 6

1
01-Jun-21

Niclosamide Dichlorophen
• Widely been used for treatment of Cestodes in dogs & • 1st synthetic anticestodal drug (1946)
cats (1960-1980)
• Administred after 12 h fasting
• Used as taeniacide in veterinary medicine for
• A laxative is required before Niclosamide many years (dogs & cats)
• A purgative is required 2 h after Niclosamide in simple • Widely used in small ruminants for Moneizia
stomach and 4 h in ruminants expansa in sheep
• Inhibition od parasites mitochodrial anerobic • For dogs & cats used with Toluene
phosphorylation of ADP
• Has inconsistent efficacy against Dipylidium spp. • Successfully removes 95% of ascarids
• Not ovicidal • Has been superceded by Praziquantel &
• Dog@50mg/Kg PO repeat after 1 week Niclosamide

7 8

Resorantel Bithionol
• Anticestodal drug for ruminants • A phenolic compound, Agrochemical(pKa4.82)
• Has been used for tapeworms in dog, cat &
• Highly effective against Moniezia spp. In both poultry
sheep & cattle • Also used for rumen flukes of sheep, goat and
• Resorantel and Oxyclosanide are drug of cattle
choice against adult and immature rumen • Readily absorbed from GIT & widely distributed
throughout the body
flukes • Withdrawn from the market after finding it a
• Also has efficacy against rumen flukes when potent photosensitizer caused serious skin
used @ 65mg/Kg PO disorders

9 10

Praziquantel Praziquantel …
• Novel anthelmintic with excellent activity against • Has a significant 1st pass effect
a wide spectrum of adult & larval cestodes of
animals and humans • Crosses BBB- an asset for larval stages
• Effective against all species of schistosomes • Quickly metabolized to inactive form in liver
pathogenic to humans
• Sparingly soluble in H2O • Renal excretion is the main route of
• Soluble in most organic solvents elimination
• Quickly & almost completely absorbed from GIT • increased F value once co-administered with
after oral administration Albendazole
• Css is achieved in 30-120 min in dogs

11 12

2
01-Jun-21

Mechanism of Action Clinical Use


• Primary effect is instantenous • In dog/cat @5mg/Kg PO @5.8mg/Kg SQ
• Rapid & sustained tetanic contraction of parasitic
musculature • Cat @12mg/Kg Spot-on
• Rapid vacoulization of the syncytial tegument • For lung flukes @25mg/Kg SID for 3 cons. Days
• Increase visible blobs above tegument surface
• Vacoulization of tegument is restricted to anterior • In combination with Febantel (Paste) and
region of strobila of tapeworm Pyrantel (Tablets)
• Metabolic changes include decrease in glucose uptake,
glycogen storage, ATP content & lactate release • Praziquantel (1-1.5mg/Kg) + Febantel (10-
• All effects are thought to be mediated by release of 15mg/Kg) used in the traetment of GI
intracelluar stored Ca++ nematodes & Cestodes for 3 consecutive days
13 14

Clinical Toxicities/Adverse Effects


• A triple combination of Praziquantel, Pyrantel • Wide margin of safety ~10x
& Oxantel is marketed as broad spectrum • Safe in breeding and pregnancies
dewormer for dogs & cats • Contraindicated for ocular Cysticercosis –
• Other combinations include Praziquantel plus destruction of organism may damage eye
Oxibendazole, Mebendazole & Fenbendazole • Contraindicated in puppies <4wks, kitten<6wks
• A recent combination of Praziquantel with • Vomiting is frequent after PO
Emodepside as broad spectrum anthelmintic • Transient injection site pain is frequent after IM
for cats

15 16

Epsiprantel Comparison
• Cestocidal compound chemically related to
Praziquantel
• Used specifically for treatment of tapeworms in
dogs & cats
• Causes tegumental damage in both adult& larva
• Fasting before administration is not necessary
• Poor GI absorption, high conc. Fecal elimination
• Practically insoluble in water
• Systemic availability after PO is negligible
• Dog @5.5mg/Kg [email protected]/Kg
17 18

You might also like