Academic Thesis

Basic information

Name Kadekaru Sho
Belonging department
Occupation name
researchmap researcher code R000032212
researchmap agency Okayama University of Science

Title

Metabolic, pathological, and genetic analyses of foals neonatal foals that died in Noma horses

Bibliography Type

Joint Author

Author

Keiichi HISAEDA, Nu Anh Thu LE, Sho KADEKARU, Tetsushi ONO, Yasuharu HIASA, Emi OHZAWA, Akihisa HATA, Kenji KUTARA, Keisuke SUGIMOTO, Yumi UNE, Eri IWATA, Tetsuo KUNIEDA, Chunhua ZHANG, Hitoshi KITAGAWA

Summary

We evaluated metabolic abnormalities in six neonatal Noma foals (Nos. 54–57, 62, and 66) that died shortly after birth, using laboratory tests, pathological examinations, serum amino acid (AA) analyses, gas chromatography/mass spectrometry (GC/MS), and genetic analyses. Nonspecific clinical symptoms, such as poor suckling and weakness, were commonly observed at birth. Sepsis caused by various bacterial infections was detected in foal Nos. 54, 62, and 66, while a heart malformation was identified in foal No. 57. Laboratory tests showed high aspartate transaminase, lactate dehydrogenase, and creatine kinase levels and low globulin and glucose levels in dead foals. The AA and GC/MS analyses revealed elevated levels of ammonia, orotic acid, and uracil in foal Nos. 54 and 55, while citrulline, arginine, and ornithine levels were low or within normal ranges, suggesting accelerated pyrimidine synthesis and suppressed urea cycle activity. Foal No. 56 had high uric acid and tyrosine levels, hypoglycemia, and liver dysfunction, suggesting glycogen storage disease. In foal No. 57, hypertyrosinemia was suggested because of high phenylalanine and tyrosine levels. We conducted a sequencing analysis of the ornithine transcarbamylase, argininosuccinatelyase, argininosuccinate synthase 1, uridine monophosphate synthase, G6PC1, and G6PT1/SLC37A4 genes associated with metabolic disorders. However, no mutations were detected. In conclusion, although metabolic pathways abnormalities resembling certain hereditary metabolic disorders were observed in neonatal foals that died in Noma horses, no specific mutations were identified in candidate genes, making hereditary disorders less likely.

Magazine(name)

Journal of Equine Science

Publisher

Volume

36

Number Of Pages

2

StartingPage

55

EndingPage

65

Date of Issue

2025/06

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

1340-3516

DOI

10.1294/jes.36.55

NAID

PMID

URL

J-GLOBAL ID

arXiv ID

ORCID Put Code

DBLP ID