PMID- 17303690 OWN - NLM STAT- MEDLINE DCOM- 20070521 LR - 20190722 IS - 0009-9147 (Print) IS - 0009-9147 (Linking) VI - 53 IP - 4 DP - 2007 Apr TI - Hyperhomocysteinemia and myocardial expression of brain natriuretic peptide in rats. PG - 773-80 AB - BACKGROUND: Hyperhomocysteinemia (HHcy) has been linked to impaired left ventricular function and clinical class in patients with chronic heart failure. We hypothesized that HHcy stimulates myocardial brain natriuretic peptide (BNP) expression and induces adverse left ventricular remodeling. METHODS: We randomized 50 rats into 5 groups. Groups Co1 and Co2 (controls) received a typical diet. Groups Meth, Hcy1, and Hcy2 were fed the same diet supplemented with 2.4% methionine, 1% homocystine, and 2% homocystine, respectively. After 12 weeks, we measured total plasma homocysteine (tHcy) and BNP in plasma and tissue, and we performed histomorphometric analyses. RESULTS: All animals had comparable baseline body weight [mean (SD) 234 (26) g] and total circulating Hcy [4.7 (1.7) micromol/L]. After 12 weeks of treatment, total circulating Hcy increased in Meth, Hcy1, and Hcy2 [27.3 (8.8), 40.6 (7.0), and 54.0 (46.0) micromol/L, respectively] and remained unchanged in Co1 and Co2. Serum BNP significantly increased in 1 of 10 animals in Meth, 3 of 10 animals in Hcy1, and 3 of 10 animals in Hcy2. Median (25th-75th percentile) BNP tissue concentrations in Hcy1 and Hcy2 were 55% higher than in the corresponding controls [Co1 vs Hcy1, 225 (186-263) vs 338 (262-410) pg/mg protein, P = 0.05; Co2 vs Hcy2, 179 (107-261) vs 308 (192-429) pg/mg protein, P = 0.12]. In the Meth group, BNP expression was comparable to that of controls [200 (159-235) vs 225 (186-263) pg/mg protein, P = 0.32]. The percentage of perivascular and interstitial collagen and mast cell infiltration were comparable in all groups, indicating no adverse cardiac remodeling. CONCLUSION: Three months of intermediate HHcy stimulated increased cardiac BNP expression that was not accompanied by adverse cardiac remodeling. FAU - Herrmann, Markus AU - Herrmann M AD - Department of Clinical Chemistry, University Hospital of Saarland, Homburg/Saar, Germany. FAU - Taban-Shoma, Omid AU - Taban-Shoma O FAU - Hubner, Ulrich AU - Hubner U FAU - Pexa, Anette AU - Pexa A FAU - Kilter, Heiko AU - Kilter H FAU - Umanskaya, Natalia AU - Umanskaya N FAU - Straub, Rainer Hans AU - Straub RH FAU - Bohm, Michael AU - Bohm M FAU - Herrmann, Wolfgang AU - Herrmann W LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070215 PL - England TA - Clin Chem JT - Clinical chemistry JID - 9421549 RN - 114471-18-0 (Natriuretic Peptide, Brain) SB - IM MH - Animals MH - Female MH - Hyperhomocysteinemia/complications/*metabolism MH - Mast Cells/pathology MH - Myocardium/*metabolism/pathology MH - Natriuretic Peptide, Brain/*biosynthesis MH - Organ Size MH - Random Allocation MH - Rats MH - Rats, Wistar MH - Ventricular Remodeling EDAT- 2007/02/17 09:00 MHDA- 2007/05/22 09:00 CRDT- 2007/02/17 09:00 PHST- 2007/02/17 09:00 [pubmed] PHST- 2007/05/22 09:00 [medline] PHST- 2007/02/17 09:00 [entrez] AID - clinchem.2006.077859 [pii] AID - 10.1373/clinchem.2006.077859 [doi] PST - ppublish SO - Clin Chem. 2007 Apr;53(4):773-80. doi: 10.1373/clinchem.2006.077859. Epub 2007 Feb 15.