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International journal for parasitology. Drugs and drug resistance2026; 31; 100642; doi: 10.1016/j.ijpddr.2026.100642

Terpenic compounds possess anthelmintic and immunomodulatory properties with potential for controlling equine cyathostomin infections.

Abstract: The emergence of anthelmintic-resistant parasite isolates necessitates alternative control strategies. The use of dietary additives with anti-parasitic or immunomodulatory activities has been proposed as a solution, but whether such additives can simultaneously exert dual bioactivities within this context has rarely been explored. Here, we evaluated whether selected terpenes could exert dual bioactivities (anti-parasitic and immunomodulatory) with a view to their use as food additives that can limit strongyle infections in horses. In vitro tests with cyathostomin larval development, larval migration, and immune modulation showed that cinnamaldehyde and carvacrol possessed high activity, and nemabiome analysis revealed that both compounds modulated cyathostomin community structure. Moreover, they also displayed significant anti-inflammatory activity in equine mononuclear cells and modulated gene expression induced by parasite antigen in monocytes, including an upregulation of an antioxidant defense network. However, no effects of cinnamaldehyde were observed on parasite egg excretion or host blood cell profiles during a 28 day in vivo feeding study. These data suggest that whilst terpenes have broad-acting bioactivities, gaps between in vitro properties and in vivo efficacy need to be overcome to realize their potential to improve host resistance to parasites.
Publication Date: 2026-04-12 PubMed ID: 42001742PubMed Central: PMC13101707DOI: 10.1016/j.ijpddr.2026.100642Google Scholar: Lookup
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  • Journal Article

Summary

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Terpenic compounds, such as cinnamaldehyde and carvacrol, show promising anti-parasitic and immunomodulatory effects against equine cyathostomin infections in laboratory tests, but their effectiveness in live horses remains uncertain.

Background and Purpose

  • Equine cyathostomins (small strongyle parasites) are common and problematic intestinal parasites in horses.
  • Resistance to conventional anthelmintic drugs is increasing, making alternative control strategies essential.
  • Dietary additives with anti-parasitic and immune system–modulating properties are proposed as sustainable control options.
  • The study aimed to determine whether certain terpenes could provide dual benefits — both killing or inhibiting parasites and modulating the horse’s immune response — for potential use as feed additives against cyathostomin infections.

Methods

  • In vitro assays were conducted to test effects of selected terpenes (including cinnamaldehyde and carvacrol) on:
    • Cyathostomin larval development (growth and maturation)
    • Larval migration ability (movement through substrates)
    • Immune modulation in equine immune cells exposed to parasite antigens
  • Nemabiome analysis: genetic sequencing was used to assess the impact of terpenes on the composition and community structure of cyathostomin populations.
  • An in vivo feeding study was performed where live horses were given cinnamaldehyde for 28 days to observe effects on:
    • Parasite egg excretion in feces
    • Host blood cell profiles (as indicators of immune status)

Key Findings

  • In vitro anti-parasitic activity: Cinnamaldehyde and carvacrol significantly inhibited cyathostomin larval development and migration.
  • Impact on parasite communities: Both compounds altered cyathostomin community structure, indicating selective effects on parasite populations.
  • Immunomodulatory effects in vitro:
    • Both terpenes reduced inflammatory responses in equine mononuclear immune cells.
    • They modulated gene expression induced by parasite antigens in monocytes, upregulating antioxidant defense pathways.
  • In vivo results: Despite promising in vitro data, cinnamaldehyde did not significantly impact parasite egg counts or blood immune cell profiles over 28 days in live horses.

Conclusions and Implications

  • Terpenes show broad-spectrum bioactivities relevant to parasite control, combining direct anti-parasitic effects with beneficial immune modulation.
  • There is a disconnect between laboratory (in vitro) efficacy and live animal (in vivo) effectiveness, highlighting challenges in translating these findings to practical therapies.
  • Further research is needed to optimize delivery methods, dosing, or combinations that can realize the potential of terpenic compounds as natural feed additives to help control cyathostomin infections and improve horse health sustainably.

Cite This Article

APA
Malsa J, Chereau A, Guégnard F, Serreau D, Gesbert A, Reigner F, Chamoin L, Guillot J, Vernudachi A, Mach N, Fleurance G, Lacroix-Lamandé S, Williams AR, Sallé G. (2026). Terpenic compounds possess anthelmintic and immunomodulatory properties with potential for controlling equine cyathostomin infections. Int J Parasitol Drugs Drug Resist, 31, 100642. https://doi.org/10.1016/j.ijpddr.2026.100642

Publication

ISSN: 2211-3207
NlmUniqueID: 101576715
Country: Netherlands
Language: English
Volume: 31
Pages: 100642
PII: 100642

Researcher Affiliations

Malsa, Joshua
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France; Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Dyrlægevej 100, 1870, Frederiksberg C, Denmark.
Chereau, Angélique
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.
Guégnard, Fabrice
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.
Serreau, Delphine
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.
Gesbert, Amandine
  • INRAE, Unité Expérimentale de Physiologie Animale de l'Orfrasière, Nouzilly, France.
Reigner, Fabrice
  • INRAE, Unité Expérimentale de Physiologie Animale de l'Orfrasière, Nouzilly, France.
Chamoin, Léonie
  • Oniris VetAgroBio, 44300, Nantes, France.
Guillot, Jacques
  • Oniris VetAgroBio, 44300, Nantes, France.
Vernudachi, Alexandre
  • INVENesis, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.
Mach, Nuria
  • IHAP, Université de Toulouse, INRAE, ENVT, Cedex 3, Toulouse, 31076, France.
Fleurance, Géraldine
  • Institut français du cheval et de l'équitation, Pôle développement, Innovation et Recherche, Saint-Genès-Champanelle, France; INRAE, Université Clermont Auvergne, VetAgro Sup, UMR 1213 Herbivores, Saint-Genès-Champanelle, France.
Lacroix-Lamandé, Sonia
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.
Williams, Andrew R
  • Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Dyrlægevej 100, 1870, Frederiksberg C, Denmark. Electronic address: arw@sund.ku.dk.
Sallé, Guillaume
  • INRAE, Université de Tours, UMR 1282 Infectiologie et Santé Publique, Nouzilly, France.

Conflict of Interest Statement

Conflict of interest statement The authors have no financial or other conflicts of interest to declare.

References

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