desmosine and Aortic-Aneurysm

desmosine has been researched along with Aortic-Aneurysm* in 4 studies

Other Studies

4 other study(ies) available for desmosine and Aortic-Aneurysm

ArticleYear
Characteristic change of urinary elastin peptides and desmosine in the aortic aneurysm.
    Biological & pharmaceutical bulletin, 1999, Volume: 22, Issue:8

    To estimate elastin metabolism in aneurysm, urinary levels of desmosine and elastin peptide in patients (n=23, range 54 to 85 years old) with aneurysm were measured by ELISA and compared between two control groups divided by age (<10 years old and >20 years old). The amounts of urinary desmosine and elastin peptide in the aneurysm group were significantly increased compared with those in the older control group (>20 years old). There was a correlation between urinary desmosine and elastin peptide in the young group. On the other hand, no such correlation was observed in the aneurysm group and the older control group. The distribution of the ratio (desmosine/elastin peptide) in the aneurysm group was different from that of the young control group. We conclude that assay of elastin peptide and desmosine in urine are useful in characterizing elastin degradation in a patient with aneurysm.

    Topics: Adult; Aged; Aged, 80 and over; Aortic Aneurysm; Child; Child, Preschool; Desmosine; Elastin; Humans; Infant; Middle Aged; Peptide Fragments

1999
Prevention of aneurysm development and rupture by local overexpression of plasminogen activator inhibitor-1.
    Circulation, 1998, Jul-21, Volume: 98, Issue:3

    Arterial aneurysms exhibit a loss of elastin and an increase in the plasminogen activators urokinase plasminogen activator (u-PA) and tissue plasminogen activator (t-PA). Because u-PA, t-PA, and plasmin have a limited proteolytic activity against elastin, the role of plasminogen activators in the aneurysmal disease is unclear. To investigate this question, we overexpressed plasminogen activator inhibitor-1 (PAI-1), an inhibitor of t-PA and u-PA, in a rat model of aortic aneurysm.. Guinea pig-to-rat aortic xenografts were seeded with syngeneic Fischer 344 rat smooth muscle cells retrovirally transduced with the rat PAI-1 gene (LPSN group) or the vector alone (LXSN group). Some grafts were not seeded with cells (NO group). Western blots showed increased PAI-1 in grafts from the LPSN group compared with LXSN and NO groups. All grafts in the NO group (n=8) and 40% in the LXSN group ruptured between days 4 and 14. At 4 weeks in the LXSN group, the remaining unruptured grafts (n=6) were aneurysmal (diameter increase > or =100%), whereas in the LPSN group (n=6) none of the grafts had ruptured or were aneurysmal. Elastin was preserved in the LPSN group. t-PA, the major PA expressed in the model, was decreased in the LPSN group compared with the other groups, as determined by zymography. Quantitative zymography showed decreased levels of two matrix metalloproteinases (MMPs), a 28-kD caseinase, and activated MMP-9 in the LPSN group.. The blockade of plasminogen activators prevents formation of aneurysms and arterial rupture by inhibiting MMP activation.

    Topics: Animals; Aorta; Aortic Aneurysm; Aortic Rupture; Desmosine; Elastin; Guinea Pigs; Immunization; Male; Metalloendopeptidases; Plasminogen Activator Inhibitor 1; Plasminogen Activators; Rats; Rats, Inbred F344; Time Factors; Tissue Plasminogen Activator; Transplantation, Heterologous

1998
Elastin content, cross-links, and mRNA in normal and aneurysmal human aorta.
    Journal of vascular surgery, 1992, Volume: 16, Issue:2

    Although elastin depletion is thought to be an etiologic factor in abdominal aortic aneurysm, little is known about its transcription and posttranslational modification in normal and diseased human aorta. Our objectives were to quantify total elastin and elastin cross-links (desmosine/isodesmosine [DID]) and to determine if elastin mRNA was detectable in the disease-prone infrarenal aorta from patients with abdominal aortic aneurysm and a comparative group with no aneurysmal diseases. After preliminary extraction and thermolysin digestion, content of DID and the elastin tetrapeptide, valine-alanine-proline-glycine (VAPG), were determined by high-performance liquid chromatography. Tissue mRNA was studied by Northern blot analysis. Mean values (+/- SE) were compared by Student's t test. The proportion of insoluble elastin was markedly decreased in abdominal aortic aneurysm tissue (1.3% +/- 0.04% vs 12% +/- -2.8%; p less than 0.001). There was no difference in the small percentage of elastin solubilized during extraction in abdominal aortic aneurysm (5.3% +/- 1%) and no aneurysmal disease (6.0% +/- 1.2%; p = 0.71) tissues. The DID concentration of insoluble elastin was not different for abdominal aortic aneurysm and no aneurysmal disease tissue (0.18% +/- 0.07 vs 0.18 +/- 0.05 nm DID/nm VAPG; p = 0.97). On the basis of VAPG content, only 26% +/- 4% of the sodium hydroxide insoluble residue from abdominal aortic aneurysm was elastin; the predominate protein(s) was high in polar amino acids. Elastin mRNA was detectable in all tissues.(ABSTRACT TRUNCATED AT 250 WORDS)

    Topics: Aged; Amino Acid Sequence; Aorta, Abdominal; Aortic Aneurysm; Blotting, Northern; Chromatography, High Pressure Liquid; Desmosine; Elastin; Humans; Isodesmosine; Linear Models; Molecular Sequence Data; RNA, Messenger; Thermolysin

1992
Desmosines in aneurysms of the ascending aorta (annulo-aortic ectasia).
    Biochimica et biophysica acta, 1982, Jul-16, Volume: 717, Issue:1

    Amino acid chromatography was used for determination of the elastin-specific amino acids desmosine and isodesmosine in acid hydrolyzates of intima-medial samples taken intraoperatively from aneurysms of human ascending aorta. Elastin concentration of the specimens was also estimated by hot alkali extraction followed by nitrogen determination of the extracted material and the insoluble residue. All patients studied had annulo-aortic ectasia i.e., dilatation of the aortic annulus and the ascending aorta. Two patients with the Marfan syndrome had low aortic elastin concentration determined by both methods. A third Marfan syndrome patient, youngest of the three, also had a slightly reduced concentration of elastin in the aorta. Aortic samples were studied from five patients who did not have the classical Marfan syndrome. Two patients of those five had decreased aortic elastin concentration. The change in elastin concentration was accompanied by high hydroxyproline/proline or hydroxylysine/lysine ratios which indicates that the proteins of the aneurysmatic aortic wall contained more collagen than the proteins of the control aortic wall. These findings point to a change in the structure or metabolism of elastin in the aortic wall in the Marfan syndrome and at least in some other patients with annulo-aortic ectasia.

    Topics: Adolescent; Adult; Amino Acids; Aorta, Thoracic; Aortic Aneurysm; Child; Desmosine; Elastin; Female; Humans; Male; Marfan Syndrome; Middle Aged

1982