Pubmed-entry ::= {
pmid 10321706,
medent {
em std {
year 1999,
month 7,
day 15
},
cit {
title {
name "Prostaglandin E1 and recombinant bone morphogenetic protein
effect on strength of hydroxyapatite implants."
},
authors {
names ml {
"Ono I",
"Tateshita T",
"Kuboki Y"
},
affil str "Department of Dermatology, Fukushima Medical University,
School of Medicine, Japan."
},
from journal {
title {
iso-jta "J. Biomed. Mater. Res.",
ml-jta "J Biomed Mater Res",
issn "0021-9304",
name "Journal of biomedical materials research"
},
imp {
date std {
year 1999,
month 6,
day 15
},
volume "45",
issue "4",
pages "337-344",
language "eng",
pubstatus ppublish,
history {
{
pubstatus pubmed,
date std {
year 1999,
month 5,
day 13,
hour 2,
minute 5
}
},
{
pubstatus medline,
date std {
year 2000,
month 6,
day 20,
hour 9,
minute 0
}
},
{
pubstatus other,
date std {
year 1999,
month 5,
day 13,
hour 2,
minute 5
}
}
}
}
},
ids {
pubmed 10321706,
pii "10.1002/(SICI)1097-4636(19990615)45:43.0.CO;2-H"
}
},
abstract "Although combinations of hydroxyapatite (HAP) and bone
morphogenetic protein (BMP) are expected to provide potent alternatives to
autogenous bone grafts, it is still anticipated that substances that act
synergistically with BMP will be found because the inducing potential of
purified BMP in bone is not strong enough. We already have shown that
prostaglandin (PG) E1 has a strong and dose-dependent synergistic effect on
the osteoinductive activity induced by recombinant human (rh) BMP and that it
enhances osteoconduction even when used alone. In this study, porous HAP rods
were treated as follows: (1) without PGE1 or rhBMP (control group); (2) with
varying concentrations of PGE1; and (3) with varying concentrations of PGE1
combined with 1 microg of rhBMP-2. The rods were subperiosteally implanted on
the cranial bone of rabbits to evaluate the effect of these treatments on the
mechanical strength of the implanted HAP rods. The HAP rods were removed 3,
6, or 9 weeks after implantation and subjected to mechanical strength
determinations. The control group (no addition of BMP to the rods) showed no
significant increase in three-point bending strength or in compression
strength compared to pre-implantation. On the other hand, PGE1 combined with
rhBMP had a strong and dose-dependent effect on the mechanical strength of
HAP, increasing it significantly, especially compression strength. PGE1 also
increased mechanical strength even when used alone. Histological examination
revealed that PGE1, whether or not it was combined with rhBMP, increased bone
formation into the pores of HAP and consequently increased the mechanical
strength of porous HAP.",
mesh {
{
term "Alprostadil",
qual {
{
mp TRUE,
subh "pharmacology"
}
}
},
{
term "Animals"
},
{
mp TRUE,
term "Biocompatible Materials"
},
{
term "Bone Development",
qual {
{
mp TRUE,
subh "drug effects"
}
}
},
{
term "Bone Morphogenetic Proteins",
qual {
{
mp TRUE,
subh "pharmacology"
}
}
},
{
term "Bone and Bones",
qual {
{
subh "anatomy & histology"
},
{
subh "drug effects"
}
}
},
{
term "Drug Synergism"
},
{
term "Humans"
},
{
mp TRUE,
term "Hydroxyapatites"
},
{
term "Rabbits"
},
{
term "Recombinant Proteins",
qual {
{
subh "pharmacology"
}
}
},
{
term "Tensile Strength"
},
{
term "Time Factors"
}
},
substance {
{
type nameonly,
name "Biocompatible Materials"
},
{
type nameonly,
name "Bone Morphogenetic Proteins"
},
{
type nameonly,
name "Hydroxyapatites"
},
{
type nameonly,
name "Recombinant Proteins"
},
{
type cas,
cit "745-65-3",
name "Alprostadil"
}
},
pmid 10321706,
pub-type {
"Journal Article"
},
status medline
}
}
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