Role of endothelin-1 in age-dependent cerebrovascular hypotensive responses after brain injury
Departments of Anesthesia and Pharmacology, University of Pennsylvania and The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104 This study was designed to compare the effect of fluid percussion brain injury (FPI) on the hypotensive cerebrovascular response in newborn and ju...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1999-11, Vol.277 (5), p.H1884-H1894 |
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Zusammenfassung: | Departments of Anesthesia and Pharmacology, University of
Pennsylvania and The Children's Hospital of Philadelphia,
Philadelphia, Pennsylvania 19104
This study was designed to compare the effect
of fluid percussion brain injury (FPI) on the hypotensive
cerebrovascular response in newborn and juvenile pigs as a function of
time postinsult and to determine the role of endothelin-1 (ET-1) in any
age-dependent differences in hypotensive cerebrovascular regulation
after injury. Ten minutes of hypotension (10-15 ml blood/kg)
decreased mean arterial blood pressure uniformly in both groups
(~45%). In the newborn, hypotensive pial artery dilation (PAD) was
blunted within 1 h, remained diminished for at least 72 h, but was
resolved within 168 h postinjury (66 ± 4, 69 ± 4, 71 ± 4, and 64 ± 4% inhibition at 1, 4, 8, and 72 h post-FPI). During
normotension, regional cerebral blood flow (rCBF) was decreased by FPI,
and hypotension further reduced the already decremented rCBF for at
least 72 h. Cerebrospinal fluid (CSF) ET-1 was increased from 26 ± 4 to 206 ± 25 pg/ml within 72 h post-FPI, whereas an ET-1
antagonist partially restored impaired hypotensive PAD and altered
hypotensive rCBF. In contrast, hypotensive PAD and altered CBF were
only inhibited for 4 h post-FPI in the juvenile (56 ± 3 and
34 ± 4% inhibition at 1 and 4 h post-FPI). CSF ET-1 was
only increased from 27 ± 4 to 67 ± 9 pg/ml at 4 h, whereas the
concentration returned to preinjury value by 8 h post-FPI. ET-1
antagonism similarly partially restored impaired hypotensive PAD and
altered hypotensive rCBF. These data show that FPI disturbs cerebral
autoregulation during hypotension both to a greater magnitude and for a
longer duration in the newborn than in the juvenile. These data suggest
that the greater FPI-induced ET-1 release in the newborn could
contribute to age-dependent differences in impaired hypotensive
cerebral autoregulation after FPI.
newborn; cerebral circulation; hemorrhagic hypotension |
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ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1999.277.5.h1884 |