The aim of the study was to ascertain whether Ce, a lanthanide that ha
s been implicated in the pathogenesis of tropical endomyocardial fibro
sis, interferes with the biosynthetic repertoire of the cardiac muscle
in vivo. Female Sprague-Dawley rats received Ce chloride iv at 1.3 mg
/kg body wt.; controls received an equal volume of physiological salin
e. Rates of protein synthesis and transcription in cardiac muscle, mea
sured in terms of incorporation of (H-3)-phenylalanine and (H-3)-uridi
ne, respectively, into trichloroacetic acid-insoluble material were fo
und to be significantly higher in Ce-treated animals. As low levels of
Ce were earlier shown to stimulate collagen as well as noncollagen pr
otein synthesis in cardiac fibroblasts in vitro, the stimulatory effec
t of the element in vivo reported here supports the speculation that i
t may influence the expression of proteins Like collagen in the heart
and contribute to their accumulation as in endomyocardial fibrosis.