To determine the existence of the kallikrein-kinin system in the heart, we
have studied in vitro and in vivo whether rat heart expresses kininogens (K
GNs). The reverse transcription-polymerase chain reaction (RT-PCR) for KGN
mRNAs demonstrated that the cardiac tissue of adult male rats expresses T-K
GN mRNA but not high-molecular-weight (H-) KGN mRNA. An intravenous injecti
on of lipopolysaccharide (LPS) resulted in a significant increase in T-KGN
mRNA levels of rat heart within 12 h. Polyacrylamide gel electrophoresis of
cDNA products generated by RT-PCR from heart mRNA using primers specific f
or either T- or low-molecular-weigh (L-) KGN revealed that rat heart expres
sed not only T-KGN gene but also L-KGN gene, and that LPS injection exclusi
vely stimulated the expression of T-KGN but not of L-KGN gene. T-KGN mRNA w
as also detected in cultured myocytes derived from fetal rat heart, and the
expression was markedly enhanced by an addition of LPS to cultures. These
results demonstrated that rat cardiomyocytes are the source of T- and L-KGN
s but not of H-KGN, and that their expression of T-KGN mRNA is stimulated b
y LPS, probably via LPS-receptor CD14. (C) 1999 Elsevier Science B.V. All r
ights reserved.