Evaluation of muscular apoptotic changes and myogenin gene expression in experimental trichinosis after stem cells and atorvastatin added to ivermectin treatment

Trichinosis is a common parasitic disease that affects the striated skeletal muscles, causing apoptotic and degenerative changes associated with myogenin expression in the affected myocytes. Hence, this study aimed to assess the ameliorative effects of stem cells and atorvastatin added to ivermectin...

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Veröffentlicht in:Experimental parasitology 2024-10, Vol.265, p.108823, Article 108823
Hauptverfasser: Hassan, Zeinab R., El-Sayed, Samar, Zekry, Kareman M., Ahmed, Samah G., Hassan Abd_Elhamid, Asmaa, Salama, Doaa E.A., Taha, Azza Kamal, Mahmoud, Nihal A., Mohammed, Shaymaa Fathy, Amin, Mona M., Mohamed, Rasha Elsayed, Eraque, Ayat M.S., Mohamed, Shimaa A., Abdelgalil, Ranya M., Atta, Shimaa Attia, Fahmy, Nermeen Talaat, Badr, Mohamed S.
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container_start_page 108823
container_title Experimental parasitology
container_volume 265
creator Hassan, Zeinab R.
El-Sayed, Samar
Zekry, Kareman M.
Ahmed, Samah G.
Hassan Abd_Elhamid, Asmaa
Salama, Doaa E.A.
Taha, Azza Kamal
Mahmoud, Nihal A.
Mohammed, Shaymaa Fathy
Amin, Mona M.
Mohamed, Rasha Elsayed
Eraque, Ayat M.S.
Mohamed, Shimaa A.
Abdelgalil, Ranya M.
Atta, Shimaa Attia
Fahmy, Nermeen Talaat
Badr, Mohamed S.
description Trichinosis is a common parasitic disease that affects the striated skeletal muscles, causing apoptotic and degenerative changes associated with myogenin expression in the affected myocytes. Hence, this study aimed to assess the ameliorative effects of stem cells and atorvastatin added to ivermectin on the infected myocytes during the muscular phase of murine trichinosis. 120 laboratory Swiss albino male mice were divided into 10 groups, and each group was subdivided into intestinal and muscular phases (each n = 6); uninfected control; untreated infected control; infected received ivermectin monotherapy; infected received atorvastatin monotherapy; infected received stem cells monotherapy; infected received ivermectin and atorvastatin dual therapy; infected received ivermectin and stem cells dual therapy; infected received atorvastatin and stem cells dual therapy; infected received ivermectin 0.2, atorvastatin 40, and stem cells triple therapy; and infected received ivermectin 0.1, atorvastatin 20, and stem cells triple therapy. Intestinal phase mice were sacrificed on the 5th day post-infection, while those of the muscular phase were sacrificed on the 35th day post-infection. Parasitological, histopathological, ultrastructural, histochemical, biochemical, and myogenin gene expression assessments were performed. The results revealed that mice that received ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden, marked improvement in the underlying muscular degenerative changes (as was noticed by histopathological, ultrastructural, and histochemical Feulgen stain assessment), lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression. Accordingly, the combination of stem cells, atorvastatin, and ivermectin affords a potential synergistic activity against trichinosis with considerable healing of the underlying degenerative sequel. [Display omitted] •Ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden.•Marked improvement in the underlying muscular degenerative changes was observed with triple therapy.•Lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression were noticed with triple therapy.•IVM has augmented therapeutic activity against trichinosis when combined with Ator and SCs.
doi_str_mv 10.1016/j.exppara.2024.108823
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Hence, this study aimed to assess the ameliorative effects of stem cells and atorvastatin added to ivermectin on the infected myocytes during the muscular phase of murine trichinosis. 120 laboratory Swiss albino male mice were divided into 10 groups, and each group was subdivided into intestinal and muscular phases (each n = 6); uninfected control; untreated infected control; infected received ivermectin monotherapy; infected received atorvastatin monotherapy; infected received stem cells monotherapy; infected received ivermectin and atorvastatin dual therapy; infected received ivermectin and stem cells dual therapy; infected received atorvastatin and stem cells dual therapy; infected received ivermectin 0.2, atorvastatin 40, and stem cells triple therapy; and infected received ivermectin 0.1, atorvastatin 20, and stem cells triple therapy. Intestinal phase mice were sacrificed on the 5th day post-infection, while those of the muscular phase were sacrificed on the 35th day post-infection. Parasitological, histopathological, ultrastructural, histochemical, biochemical, and myogenin gene expression assessments were performed. The results revealed that mice that received ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden, marked improvement in the underlying muscular degenerative changes (as was noticed by histopathological, ultrastructural, and histochemical Feulgen stain assessment), lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression. Accordingly, the combination of stem cells, atorvastatin, and ivermectin affords a potential synergistic activity against trichinosis with considerable healing of the underlying degenerative sequel. [Display omitted] •Ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden.•Marked improvement in the underlying muscular degenerative changes was observed with triple therapy.•Lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression were noticed with triple therapy.•IVM has augmented therapeutic activity against trichinosis when combined with Ator and SCs.</description><identifier>ISSN: 0014-4894</identifier><identifier>ISSN: 1090-2449</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/j.exppara.2024.108823</identifier><identifier>PMID: 39187057</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis ; Apoptosis - drug effects ; Atorvastatin ; Atorvastatin - pharmacology ; Atorvastatin - therapeutic use ; Feulgen ; Gene Expression - drug effects ; Ivermectin - pharmacology ; Ivermectin - therapeutic use ; Male ; Mice ; Microscopy, Electron, Transmission ; Muscle, Skeletal - drug effects ; Muscle, Skeletal - parasitology ; Muscle, Skeletal - pathology ; Myogenin ; Myogenin - genetics ; Myogenin - metabolism ; Stem Cell Transplantation ; Stem cells ; Stem Cells - drug effects ; Trichinella spiralis - drug effects ; Trichinella spiralis - genetics ; Trichinellosis - drug therapy ; Trichinellosis - parasitology ; Trichinosis</subject><ispartof>Experimental parasitology, 2024-10, Vol.265, p.108823, Article 108823</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c313t-42fb12f5f11a18f639ba376f3bb0077b008d15cb7318ef0f360e262caa2f497c3</cites><orcidid>0009-0008-3809-3819 ; 0000-0001-8980-9196 ; 0000-0002-6767-6764 ; 0000-0003-1307-9320</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014489424001267$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39187057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hassan, Zeinab R.</creatorcontrib><creatorcontrib>El-Sayed, Samar</creatorcontrib><creatorcontrib>Zekry, Kareman M.</creatorcontrib><creatorcontrib>Ahmed, Samah G.</creatorcontrib><creatorcontrib>Hassan Abd_Elhamid, Asmaa</creatorcontrib><creatorcontrib>Salama, Doaa E.A.</creatorcontrib><creatorcontrib>Taha, Azza Kamal</creatorcontrib><creatorcontrib>Mahmoud, Nihal A.</creatorcontrib><creatorcontrib>Mohammed, Shaymaa Fathy</creatorcontrib><creatorcontrib>Amin, Mona M.</creatorcontrib><creatorcontrib>Mohamed, Rasha Elsayed</creatorcontrib><creatorcontrib>Eraque, Ayat M.S.</creatorcontrib><creatorcontrib>Mohamed, Shimaa A.</creatorcontrib><creatorcontrib>Abdelgalil, Ranya M.</creatorcontrib><creatorcontrib>Atta, Shimaa Attia</creatorcontrib><creatorcontrib>Fahmy, Nermeen Talaat</creatorcontrib><creatorcontrib>Badr, Mohamed S.</creatorcontrib><title>Evaluation of muscular apoptotic changes and myogenin gene expression in experimental trichinosis after stem cells and atorvastatin added to ivermectin treatment</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>Trichinosis is a common parasitic disease that affects the striated skeletal muscles, causing apoptotic and degenerative changes associated with myogenin expression in the affected myocytes. Hence, this study aimed to assess the ameliorative effects of stem cells and atorvastatin added to ivermectin on the infected myocytes during the muscular phase of murine trichinosis. 120 laboratory Swiss albino male mice were divided into 10 groups, and each group was subdivided into intestinal and muscular phases (each n = 6); uninfected control; untreated infected control; infected received ivermectin monotherapy; infected received atorvastatin monotherapy; infected received stem cells monotherapy; infected received ivermectin and atorvastatin dual therapy; infected received ivermectin and stem cells dual therapy; infected received atorvastatin and stem cells dual therapy; infected received ivermectin 0.2, atorvastatin 40, and stem cells triple therapy; and infected received ivermectin 0.1, atorvastatin 20, and stem cells triple therapy. Intestinal phase mice were sacrificed on the 5th day post-infection, while those of the muscular phase were sacrificed on the 35th day post-infection. Parasitological, histopathological, ultrastructural, histochemical, biochemical, and myogenin gene expression assessments were performed. The results revealed that mice that received ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden, marked improvement in the underlying muscular degenerative changes (as was noticed by histopathological, ultrastructural, and histochemical Feulgen stain assessment), lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression. Accordingly, the combination of stem cells, atorvastatin, and ivermectin affords a potential synergistic activity against trichinosis with considerable healing of the underlying degenerative sequel. 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Hence, this study aimed to assess the ameliorative effects of stem cells and atorvastatin added to ivermectin on the infected myocytes during the muscular phase of murine trichinosis. 120 laboratory Swiss albino male mice were divided into 10 groups, and each group was subdivided into intestinal and muscular phases (each n = 6); uninfected control; untreated infected control; infected received ivermectin monotherapy; infected received atorvastatin monotherapy; infected received stem cells monotherapy; infected received ivermectin and atorvastatin dual therapy; infected received ivermectin and stem cells dual therapy; infected received atorvastatin and stem cells dual therapy; infected received ivermectin 0.2, atorvastatin 40, and stem cells triple therapy; and infected received ivermectin 0.1, atorvastatin 20, and stem cells triple therapy. 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[Display omitted] •Ivermectin, atorvastatin, and stem cell triple therapies showed the maximum reduction in the adult worm and larvae burden.•Marked improvement in the underlying muscular degenerative changes was observed with triple therapy.•Lower biochemical levels of serum NK-κB and tissue NO, and lower myogenin expression were noticed with triple therapy.•IVM has augmented therapeutic activity against trichinosis when combined with Ator and SCs.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39187057</pmid><doi>10.1016/j.exppara.2024.108823</doi><orcidid>https://orcid.org/0009-0008-3809-3819</orcidid><orcidid>https://orcid.org/0000-0001-8980-9196</orcidid><orcidid>https://orcid.org/0000-0002-6767-6764</orcidid><orcidid>https://orcid.org/0000-0003-1307-9320</orcidid></addata></record>
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1090-2449
1090-2449
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subjects Animals
Apoptosis
Apoptosis - drug effects
Atorvastatin
Atorvastatin - pharmacology
Atorvastatin - therapeutic use
Feulgen
Gene Expression - drug effects
Ivermectin - pharmacology
Ivermectin - therapeutic use
Male
Mice
Microscopy, Electron, Transmission
Muscle, Skeletal - drug effects
Muscle, Skeletal - parasitology
Muscle, Skeletal - pathology
Myogenin
Myogenin - genetics
Myogenin - metabolism
Stem Cell Transplantation
Stem cells
Stem Cells - drug effects
Trichinella spiralis - drug effects
Trichinella spiralis - genetics
Trichinellosis - drug therapy
Trichinellosis - parasitology
Trichinosis
title Evaluation of muscular apoptotic changes and myogenin gene expression in experimental trichinosis after stem cells and atorvastatin added to ivermectin treatment
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