(Hypertension. 2001;37:313.)
© 2001 American Heart Association, Inc.
Scientific Contributions |
Pulse Pressure, Aortic Reactivity, and Endothelium Dysfunction in Old Hypertensive Rats
From the Department of Internal Medicine and INSERM, U337, Broussais Hospital, Paris (M.E.S.), and the Medical Research Department (P.C.-C.), CNRS ESA 8078, Marie Lannelongue Hospital, 92350 Le Plessis-Robinson, France (J.F.R., P.C.- C.).
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsReferences |
|---|
The reactivity of old hypertensive rat aortas has not been investigated in relation to each phenotype of the blood pressure curve, mean arterial pressure (MAP), and pulse pressure (PP). Aortic reactivities from 3- to 78-week-old Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR) were studied with the use of organ chambers and invasive blood pressure, carotid diameter, and histomorphometry. MAP and PP were elevated in SHR, but at 78 weeks, a selective increase of PP without further MAP increase was observed for the same carotid diameter as WKY. Aortic relaxation in response to carbamylcholine decreased similarly with age in both strains. With (+) or without (-) endothelium (E), maximal developed tension (MDT) under KCl increased linearly with age in SHR, proportionally to wall thickness and MAP increase. Under norepinephrine (NE), MDT of E- aortas from SHR and controls increased with age and reached plateaus at 12 weeks, whereas MDT of E+ aortas from SHR increased linearly with age. Because the NE-induced MDT was higher for E- than E+, the difference estimated endothelial function. This difference reached plateaus from 12 to 78 weeks in WKY but was abolished beyond 12 weeks in SHR, a finding also observed under NO-synthase inhibition. In old hypertensive rats, (1) increased KCl reactivity is endothelium independent but influenced by the MAP-dependent aortic hypertrophy with resulting increased vascular smooth muscle reactivity, whereas (2) increased NE reactivity is endothelium dependent in association with increased PP, altered endothelial function, and extracellular matrix, with resulting enhanced intrinsic arterial stiffness.
Key Words: rats, spontaneously hypertensive • arteries • endothelium • pulse pressure
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsReferences |
|---|
In hypertension, the blood pressure (BP) curve results from the summation of a steady component, mean arterial pressure (MAP), and a pulsatile component, pulse pressure (PP).1 The relative contributions of the two components of the BP curve are influenced significantly by age, hence by the level of arterial stiffness, one of the major determinants of PP. In younger populations of rats and humans, isobaric carotid and aortic rigidities are similar to those of normotensive controls,2 3 4 in association with proportional increases of MAP and PP.1 5 In the older populations, particularly in humans and some strains of hypertensive rats,6 7 8 isobaric carotid and aortic rigidities are reduced, indicating pressure-independent alterations of the stiffness of wall material,6 7 8 with a disproportional increase of PP over MAP but no increase of stroke volume.1 6 7 8 9 This hemodynamic pattern is usually considered a direct consequence of structural changes within the aortic wall.1 6 7 8 However, acute administration of the exogenous NO-donor sodium nitroprusside is able to reverse the increase of PP (see reviews in References 1 and 101 10 ),1 10 thus, independent of structural vascular changes. In other words, in old hypertensive animals and humans, the contributions of vasomotor tone and of NO-dependent alterations should be taken into account in the mechanism of increased aortic stiffness and PP. Because endothelium function is highly influenced by age,11 12 13 its change should be considered in parallel.
We have previously shown that in Wistar-Kyoto rats (WKY) and spontaneously hypertensive rats (SHR), an intact endothelium (E+) is required to achieve a normal relation between PP and pulsatile diameter.14 15 In the absence of endothelium (E-), carotid and abdominal arterial diameters are increased, suggesting a major role of vasoconstrictive agents in this alteration. Because the function of endothelium is not only to relax vascular smooth muscle (VSM) through NO formation and/or release but to modulate the response of the vessels to vasoconstrictive stimuli,11 13 16 this latter adjustment may interfere critically in the control of the relation between PP and pulsatile diameter and hence arterial stiffness and PP.
In SHR, sympathetic overactivity is
present.9 17
Central conduit arteries are hyperresponsive to 
-adrenergic receptor
stimulation and blockade,5
associated with an increased affinity of VSM -adrenergic
receptors.18 This
characteristic feature is of major importance because at the level of
the carotid arterial bed, we and others have shown that the
vasoconstrictive properties of
norepinephrine (NE) are counterbalanced by NO formation
and/or
release.11 12 13 16 19 20
This mechanism is operating in young
SHR,20 21 but its
relevance in old hypertensive rats has not been fully investigated. In
this study, our working hypothesis is that an age-related change of the
endothelial NE–NO interaction is an important target
mechanism that explains, in old hypertensive rats, the presence of a
pressure-independent increase of arterial stiffness with
resulting PP increase.
In this study, we investigated at different ages the aortic reactivity of SHR by comparison with normotensive WKY controls. The first objective was to show that, with the use of organ-chamber experiments, the contractile responses to NE of E+ and E- thoracic aortas reflected specific age-related changes of the NE–NO interactions in SHR and differed from the responses to KCl. The second objective was to attempt to correlate such alterations to the increased arterial stiffness and PP already observed and described in old hypertensive animals and humans.1 6 7 8
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsReferences |
|---|
All procedures were carried out in accordance with institutional guidelines for animal experimentation. Male SHR (n=35) and WKY (n=35) were studied at 3 (n=8), 5 (n=18), 12 (n=26), 52 (n=8), and 78 (n=10) weeks of age. They were obtained from Iffa-Credo, Lyon, France. Body weights of WKY and SHR, respectively, were at 3 weeks, 70±1 and 62±1 g; at 5 weeks, 165±1 and 130±1 g; at 12 weeks, 369±2 and 315±1 g; at 52 weeks, 486±7 and 443±6 g; at 78 weeks, 698±4 and 489±3 g. Animals were housed in the same environment and allowed free access to food and water at 25°C and exposed to a 12-hour light/dark cycle.
Rats were anesthetized with 50 mg/kg IP pentobarbital. A Teflon catheter (0.9-mm ID) filled with saline and coupled to a Statham P2S1D pressure transducer (Gould Statham) was inserted through the right common carotid artery and placed in the middle of the lumen for intra-arterial BP measurements. In parallel, carotid arterial diameter was determined noninvasively with an echo-tracking ultrasound technique, previously described and validated.2 3 22 With this procedure, mean diameter is calculated from the integral of its measured pulsatile changes, with a coefficient of variability of 3%. Because we previously published diameter measurements of rats 12 weeks of age,5 we limited the carotid determinations to 6 SHR that were 12 and 52 weeks old and 6 WKY and 6 SHR rats that were 78 weeks old.
The procedure for organ-chamber experiments has been
described in detail
elsewhere.11 12 13 18
Rings from thoracic aorta were equilibrated for 45 to 60 minutes. They
were stretched progressively and exposed repeatedly to 40 mmol/L
KCl to induce contraction for each new level of stretching until a
maximal contractile response to KCl was obtained (40 mmol/L, a
submaximal concentration independent of age and species). This basal
tension was considered the optimal point on a length-tension curve.
E+ and E-
experiments were performed in parallel. Endothelium was
considered to be intact when carbamylcholine
(10-9/10-5
mol/L) caused complete relaxation of rings precontracted with
3x10-7 mol/L NE and effectively removed
when carbamylcholine did not induce
relaxation.11 12 13 18
The -adrenergic contraction was evaluated by addition of cumulative
NE concentrations
(10-9/10-5
mol/L). Thereafter, the endothelium-independent
relaxation elicited by 10-5 mol/L
papaverine was studied on the same aortic preparations precontracted by
3x10-7 mol/L NE, and, finally,
vasorelaxation in response to carbamylcholine was investigated.
Concentration of the drugs are expressed as final molar (mol/L) or
millimolar (mmol/L).
For the analysis of dose-response curves, the
response was expressed as the percentage of the preceding contraction
for relaxation-eliciting agents. For contraction-inducing agents, the
response was expressed as the absolute change of maximal developed
tension (MDT, in mg). On the basis of the analysis of
dose-response curves to KCl and NE obtained from preliminary
experiments, MDT was achieved with 30 mmol/L KCl and
3x10-7 mol/L NE concentrations,
independent of age and strain. For both relaxing and contracting
agents, the concentrations inducing 50% of the maximal effect were
expressed as pD2 values and calculated with the
use of specific software (Microcalô Software
Inc).18 Finally, from the
dose-response curves studied plotted for each aorta’s
E+ and E-
responses, we defined 2 indexes of endothelial function
for this, and calculated the differences between the NE-induced MDT of
E- and the MDT of
E+. The
(E-–E+)
difference was called 
NE and used as an index of the NE-dependent
participation of the endothelium during aging. In some
experiments, the NO-synthase inhibitor
N
-nitro-L-arginine
(LNNA) (10-4 mol/L) was added to the
preparation in which the -adrenergic contractions were measured. The
increase of MDT under this inhibitor, called LNNA, was
used as an index of NO-dependent endothelial function
and, consequently, NE-NO interactions. Potassium chloride,
carbamylcholine chloride, and norepinephrine bitartrate
salt (Arterenol) were purchased from Sigma Chemical Co. All the drugs
were dissolved in distilled water and prepared daily. At the end of the
experiments, the histomorphometric parameters of the
thoracic aorta were determined, as previously described for rats 3, 5,
12, and 78 weeks
old.23
For statistical analyses, mean±1 SEM values are given. For each animal, each dose-response curve was derived from the means of 3 to 6 aortic rings. For all the animals in each subgroup, MDT and pD2 were calculated. The aortic responses were analyzed by a 2-way ANOVA. To evaluate the age-related changes of MDT, 3 different models (linear, semilogarithmic, and hyperbolic) were used, enabling linear relation to be distinguished from those reaching a plateau. A 2-way ANOVA was used to show that for each strain, MDT E- was significantly higher than MDT E+ at different ages. A value of P<0.05 was considered to be significant after Bonferroni and post hoc tests had been performed.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsReferences |
|---|
Intra-Arterial BP, Carotid Diameter, and Histomorphometric Changes
Figure 1 summarizes the BP changes between 5 and 78 weeks of age. For both strains, MAP increased with age (P<0.01), reaching plateaus at 12 weeks of age (Figure 1, upper panel). MAP was significantly higher in SHR than in WKY (P<0.01). At 12 and 52 weeks, carotid diameters measured in SHR at operational MAP were, respectively, 1048±41 and 1315±24 µm (NS). At 78 weeks of age, MAP was 183±7 mm Hg in SHR and 136±4 mm Hg in WKY (P<0.001), whereas operational carotid diameters did not differ significantly (1149±26 versus 1124±29 µm). Thus, at 78 weeks of age, the same diameter was achieved in the presence of higher MAP values in SHR, indicating a pressure-independent increase of carotid stiffness in old SHR.
|
PP was significantly higher in SHR than in WKY (P<0.01) (Figure 1, lower panel). Although PP was practically unchanged with age in WKY, it increased significantly with age in SHR (P<0.05), particularly from 52 to 78 weeks (P<0.01), resulting in a significant interaction (P<0.01) with normotensive WKY controls.
Table 1 indicates that medial cross-sectional area (MCSA), collagen content, and the collagen/elastin ratio increased significantly with age (P<0.005), with significantly higher values in SHR, particularly at 78 weeks of age (interaction: P<0.005). For the elastin content, there was a highly significant age effect without strain effect and a slight significant interaction (P<0.05).
|
VSM Relaxation Induced by Carbamylcholine
and Papaverine
For both strains, endothelium-dependent
carbamylcholine-induced relaxation was reduced significantly
(P<0.005) with age in
association with previously
described11 12 13
prostaglandin-mediated contractions at the higher
concentrations
(Figure 2). Between 3 and 12 weeks, age-related changes were
more marked in SHR than WKY, causing slightly less relaxation in SHR
than in WKY at 12 weeks
(P<0.05). Finally, obvious
differences in the age-related kinetics of relaxation were seen between
the two strains (interaction:
P=0.05). In contrast,
non–endothelium-dependent relaxation by papaverine was
the same for WKY and SHR and decreased slightly with age
(P<0.02) (data not
shown).
|
VSM Contraction Under KCl
The dose-response curves of MDT in response to
increasing KCl concentrations are shown in
Figure 3, A and B, respectively. In both strains,
significantly (P<0.005) higher
MDT values were obtained at 12, 52, and 78 weeks than at 3 and 5 weeks,
with markedly enhanced SHR responses especially at 78 weeks. In
Figure 3C, MDT was evaluated as function of age in WKY and
SHR. Whereas MDT increased with age until 12 weeks in WKY and then did
not change significantly until 78 weeks, a progressively increasing
linear relation was observed for SHR, resulting in a significantly
higher MDT in SHR than in WKY at 78 weeks of age
(P<0.005). In SHR, MDT and
MCSA were significantly, positively and linearly correlated
(r=0.70). In WKY, a plateau was
reached at 12 weeks (r=0.41).
All these results were observed with E-
aortas but did not differ for E+
preparations (data not shown).
|
VSM Contraction Under NE
The dose-response curves, plotting MDT against
increasing NE concentrations obtained with
E+ (upper panels) and
E- (lower panels) thoracic aortas from WKY
(left side; A, C) and SHR (right side; B, D), are shown in
Figure 4. First, regardless of the strain and the presence
or absence of endothelium, MDT increased with age, with
significantly higher values at 12, 52, and 78 weeks than at 3 and 5
weeks. Second, MDT was significantly higher with
E- than E+
regardless of age and strain
(P<0.001), except for older
SHR (interaction: P<0.01) (see
below). Third, the MDT responses of SHR were higher than those of WKY,
but this enhancement was observed only for
E+ aorta, particularly in older animals (see
below).
|
Table 2 indicates the pD2 values for WKY and SHR. With E- preparations, pD2 decreased with age (P<0.005), and this reduction was more pronounced in SHR (P<0.05), particularly at 52 and 78 weeks. No significant changes were seen with E+ aortas.
|
NE-induced changes of MDT as a function of age were significant for both E+ and E- preparations (P<0.005) (Figure 5). Although the MDT of E+ aortas from WKY remained relatively stable after 12 weeks of age, SHR value increased linearly with age, resulting in significantly higher MDT in SHR than in WKY at 52 and 78 weeks (P<0.005). With E- aortas, MDT did not differ and increased similarly for both strains, stabilizing between 12 and 78 weeks.
|
Indexes of NE-Dependent
Endothelial Function
NE, indicated as
Tmax(E-)-Tmax(E+)
in
Figure 6, increased with age up to 12 weeks for WKY and then
achieved a plateau. A similar pattern was observed for LNNA (data
not shown). For SHR, NE also increased with age, with even higher
values than in WKY between 3 and 12 weeks of age
(Figure 6). Thereafter, NE fell sharply and was
significantly lower than in WKY
(P<0.005). A similar pattern
was observed for SHR LNNA, which decreased markedly from 52 to 78
weeks of age
(Figure 7). Finally, for 78-week old SHR, NE
(Figure 6) and LNNA
(Figure 7) were strongly reduced, whereas PP was selectively
increased
(Figure 1).
|
|
Comments
In agreement with results previously reported in the
literature,1 7 8
we observed that MAP and PP were increased in SHR as compared with
normotensive controls. However, whereas in both strains MAP almost
reached a plateau at 12 weeks of age, PP increased sharply at 78 weeks
only in SHR. This enhancement was associated with increased intrinsic
carotid arterial stiffness, aortic MCSA, and
collagen/elastin ratio but mostly with substantial changes of aortic
reactivity. First, endothelium-dependent and
non–endothelium-dependent relaxations were
significantly reduced with age but were not influenced by the presence
of hypertension. Second, VSM contractions were stronger in old
hypertensive rats, but their extent differed markedly depending, on
whether membrane depolarization was induced by KCl or NE. Contractions
under KCl were endothelium independent and associated
MAP and the degree of VSM hypertrophy. Contractions under
NE were endothelium dependent and involved complex
interactions between NE and NO, particularly at 78 weeks of age, in
association with the selective PP increase.
It has previously been reported that arterial endothelium-dependent relaxation is reduced in mature SHR.11 12 13 24 However, this alteration is known to be not uniform, depending on the model and the vascular bed studied.13 24 In this report, the carbamylcholine-induced relaxation was slightly reduced in 12-week-old SHR compared with WKY controls, but the overall reduction of relaxation was mainly influenced by age. For both strains, similar decreases with age were observed but with obvious kinetic differences, leading to steeper reduction of relaxation with age in younger SHR than in controls (Figure 2). These results strongly suggest that age, more than the increase of BP, was the main factor acting on the reduction of aortic smooth muscle relaxation in rats.
In this study, aortic smooth muscle contractions under KCl were increased in old hypertensive rats and were proportional to the development of VSM hypertrophy. Folkow et al17 postulated that according to LaPlace’s law, resistant vessels in hypertensive rats undergo structural changes, causing the medial layer to thicken and resulting in a geometrically related increased response to vasoactive stimuli. The data reported here extend this alteration to hypertensive conduit arteries, with 3 particularities. First, according to LaPlace’s law, this change concerns exclusively the steady component of BP, MAP.17 Second, the increased reactivity occurs in proportion with the degree of increased MCSA that develops very early (Table 1), at a period during which there is no pressure-independent increase of arterial stiffness.2 3 8 10 Third, the KCl-induced contractions are not endothelium dependent and thus differ markedly from those observed under NE.
In SHR, although a number of vasoactive stimuli such as
endothelin or prostanoids may act on the vessel wall through changes in
endothelial
function,11 24 NE
is certainly of major importance because activation of the sympathetic
nervous system is a characteristic hallmark of these animals. In
agreement with a previous
study,18 our VSM
pD2 values obtained with
E- aortic rings were significantly lower
for SHR, indicating an altered muscle structure-activity coupling.
Within this framework, a major function of endothelium
is to modulate the response of VSM cells to contractile agents. NE acts
on the endothelial cells to increase NO formation
and/or release, thus attenuating its own contractile effect on
VSM.19 20 21
In our experiments, this mechanism was operating, as shown from the
experiments involving LNNA. However, whereas these responses,
represented by the two calculated indexes of
endothelial function, NE and LNNA, were observed
at all ages in WKY, they differed markedly in younger and older
SHR.
In younger SHR, we found that NE was maintained and was
even higher than in controls
(Figure 6). Numerous molecular biology studies have shown
that NO formation and/or release is upregulated in young SHR and should
be considered a compensatory mechanism for the presence of neurogenic
vasoconstriction.10 11 13 18 19 20 21 24
In parallel, we and
others2 3 4 5
have observed that in younger rats, carotid arterial
diameter and isobaric distensibility did not differ in WKY and SHR
strains, whereas BP and arterial wall thickness were higher
in hypertensive than in normotensive animals. Thus in SHR, the altered
NE-NO interaction contributes to the maintenance of normal
arterial function and proportional increases of MAP and PP
in the face of severe constrictive
influences.5
In 78-week-old hypertensive rats, we observed that compared
with WKY of the same age, NE and LNNA were significantly reduced
or even abolished, in association with increased intrinsic
arterial stiffness and PP. Several reported findings may
point to a specific link between altered endothelial
function and increased PP. First, in vitro experiments showed that NO
release and endothelial NO-synthase mRNA and protein,
which are markedly influenced by
age,25 26 are
more significantly associated with pulsatile than steady mechanical
factors.27 Second, in old
hypertensive animals and humans, exogenous NO donors are able to
normalize PP acutely and selectively, with minor changes of MAP and no
alteration of the structure of the hypertrophied and stiffened
arterial
vessels.1 6 10
This acute change occurs in older but not in younger populations, for
example, in the presence of an age-induced alteration of the
endothelium.6 11 12 13
Finally, in a recent study on the response of aortic rings to the
diuretic agent
cicletanine,28 we observed
that this compound induced NO- and
endothelium-dependent relaxation, which was mainly due
to stimulation of NO-synthase and was more pronounced in older animals.
In vivo, cicletanine was shown to produce a MAP-independent decrease of
arterial stiffness and
PP.29
In conclusion, KCl- and NE-dependent aortic reactivities are increased in old SHR. The former is endothelium independent and associated with MAP, whereas the latter is endothelium dependent and more directly related to PP. Increased PP may be due not only to modified composition of the arterial wall but also to changes in vasomotor tone of endothelial origin mainly involving altered NE-NO interactions.
|
Acknowledgments |
|---|
This study was performed with the financial support of INSERM, Association Claude-Bernard and GPH-CV. We thank Anne Safar and Pr Bernard Levy for their help.
|
Footnotes |
|---|
Correpondence to Professeur Michel Safar, Médecine Interne 1 Hôpital Broussais 96 rue Didot, 75674 Paris Cedex 14 France.
Received June 1, 2000; first decision July 24, 2000; accepted August 7, 2000.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsReferences |
|---|
1. Nichols WW, O’Rourke M. McDonald’s Blood Flow in Arteries. Theoretical, Experimental and Clinical Principles. 4th ed. London/Sydney/Auckland: Arnold E; 1998:54–113, 201–222, 284–292, 347–401.
2.
Laurent S.
Arterial wall hypertrophy and stiffness in
essential hypertensive patients.
Hypertension. 1995;26:355–362.
3. Zanchi A, Brunner HR, Hayoz D. Age-related changes of the mechanical properties of the carotid artery in spontaneously hypertensive rats. J Hypertens. 1997;15:1415–1422.[Medline] [Order article via Infotrieve]
4.
Bezie Y, Lamazier
JM, Laurent S, Challande P, Cunha RS, Bonnet J, Lacolley P.
Fibronectine expression and aortic wall elastic modulus in
spontaneously hypertensive rats.
Arterioscler Thromb Vasc Biol. 1998;18:1027–1034.
5.
Cunha R, Dabire H,
Bezie I, Weiss AM, Chaouche-Teyara K, Laurent S, Safar M, Lacolley P.
Mechanical stress of the carotid artery at the early phase of
spontaneous hypertension in rats.
Hypertension. 1997;29:992–998.
6. Simon AC, Safar ME, Levenson JA, Kheder AM, Levy BI. Systolic hypertension: hemodynamic mechanism and choice of antihypertensive treatment. Am J Cardiol. 1979;44:505–511.[Medline] [Order article via Infotrieve]
7. Atkinson J. Vascular calcium overload. Drugs. 1992;44(suppl 1):111—118.
8.
Marque V, Kieffer
P, Atkinson J, Lartaud-Idjouadienne I. Elastic properties and
composition of the aortic wall in old spontaneously hypertensive rats.
Hypertension. 1999;34:415–422.
9.
Pfeffer JM, Pfeffer
MA, Fishbein MC, Frohlich ED. Cardiac function and morphology with
aging in the spontaneously hypertensive rat.
Am J Physiol. 1979;237:H461–H468.
10.
Safar ME, Blacher
J, Mourad JJ, London GM. Stiffness of carotid artery wall material and
blood pressure in humans.
Stroke. 2000;31:782–790.
11.
Küng CF,
Lüscher TF. Different mechanisms of endothelial
dysfunction with aging and hypertension in rat aorta.
Hypertension. 1995;25:194–200.
12. Marin J. Age-related changes in vascular responses: a review. Mech Ageing Dev. 1995;79:71–114.[Medline] [Order article via Infotrieve]
13.
Barton M,
Cosentino F, Brandes RP, Moreau P, Shaw S, Lüscher F. Anatomic
heterogeneity of vascular aging: role of nitric oxide
and endothelin. Hypertension. 1997;30:817–824.
14.
Levy BI,
Benessiano J, Poitevin P, Safar ME.
Endothelium-dependent mechanical properties of carotid
artery in WKY and SHR: role of angiotensin converting
enzyme inhibition. Circ Res. 1990;66:321–328.
15.
Boutouyrie P,
Bezie Y, Lacolley P, Challande P, Chamiot-Clerc PH, Benetos A, Renaud
de la Faverie JF, Safar M, Laurent S. Wall viscosity of abdominal
aorta: in vivo and in vitro comparison: influence of
endothelial function.
Arterioscler Thromb Vasc Biol. 1997;17:1346–1355.
16. Moncada S, Palmer RMJ, Higgs EA. Nitric oxide: physiology, pathophysiology and pharmacology. Pharmacol Rev. 1991;43:109—142.[Medline] [Order article via Infotrieve]
17. Folkow B. Structural factor in primary and secondary hypertension. Hypertension. 1990;16:89–101.
18. Chamiot-Clerc PH, Colle M-H, Legrand M, Sassard J, Safar ME, Renaud J-F. Evidence for a common defect associated to the pressure in the aorta of two hypertensive rats. Clin Exp Pharmacol Physiol. 1999;26:883–888.[Medline] [Order article via Infotrieve]
19. Cocks TM, Angus JA. Endothelium-dependent relaxation of coronary arteries by noradrenaline and serotonin. Nature. 1983;305:627–630.[Medline] [Order article via Infotrieve]
20. Nishida Y, Ding J, Zhou M-S, Chen Q-H, Murkami H, Wu X-Z, Kosaka H. Role of nitric oxide in vascular hyper-responsiveness to norepinephrine in hypertensive Dahl rats. J Hypertens. 1998;16:1611–1618.[Medline] [Order article via Infotrieve]
21.
Radaelli A,
Mircoli L, Mancia G, Ferrari AU. Nitric oxide-dependent vasodilation in
young spontaneously hypertensive rats.
Hypertension. 1998;32:735–739.
22. Lacolley P, Ghodsi N, Glazer E, Challande P, Brisac AM, Safar ME, Laurent S. Influence of graded changes in vasomotor tone on the carotid arterial mechanics in live spontaneously hypertensive rats. Br J Pharmacol. 1995;115:1235–1244.[Medline] [Order article via Infotrieve]
23.
Albaladejo P,
Bouaziz H, Duriez M, Gohlke P, Levy B, Safar M, Benetos A.
Angiotensin converting enzyme inhibition prevents the
increase in aortic collagen in rats.
Hypertension. 1994;23:74–82.
24. Ruschitzka F, Corti R, Noll G, Lüscher TF. A rationale for treatment of endothelial dysfunction in hypertension. J Hypertens. 1999;17(suppl 1):S25–S35.
25.
Cernadas MR, de
Miguel LS, Garcia-Duran M, Gonzalez-Fernandez F, Millas I, Monton M,
Rodrigo J, Rico L, Fernandez P, de Frutos T, Rodriguez-Feo JA, Guerra
J, Caramelo C, Casado S, Lopez-Farre A. Expression of constitutive and
inducible nitric oxide synthases in the vascular wall of young and
aging rats. Circ Res. 1998;83:279–286.
26.
Bauersachs J,
Bouloumié A, Mülsch A, Wiemer G, Fleming I, Busse R. Vasodilator
dysfunction in aged spontaneously hypertensive rats: changes in NO
synthase III and soluble guanylate cyclase expression and
in superoxide anion production.
Cardiovasc Res. 1998;37:772–779.
27.
Hutcheson IR,
Griffith TM. Release of endothelium-derived relaxing
factor is modulated both by frequency and amplitude of pulsatile flow.
Am J Physiol. 1991;261:H257–H262.
28. Chamiot-Clerc P, Choukri N, Legrand M, Droy-Lefay MT, Safar ME, Renaud JF. Relaxation of vascular smooth muscle by cicletanine in aged Wistar aorta under stress conditions. Am J Hypertens. 2000;13:208–213.[Medline] [Order article via Infotrieve]
29. Levy B, Curmi P, Poitevin P, Safar ME. Modifications of the arterial mechanical properties of normotensive and hypertensive rats without arterial pressure changes. J Cardiovasc Pharmacol. 1989;14:253–259. [Medline] [Order article via Infotrieve]
This article has been cited by other articles:
 |
|
 |
|
  G. F. Mitchell, V. Gudnason, L. J. Launer, T. Aspelund, and T. B. Harris Hemodynamics of Increased Pulse Pressure in Older Women in the Community-Based Age, Gene/Environment Susceptibility-Reykjavik Study Hypertension, April 1, 2008; 51(4): 1123 - 1128. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 E. Cosson, M. Herisse, D. Laude, F. Thomas, P. Valensi, J.-R. Attali, M. E. Safar, and H. Dabire Aortic stiffness and pulse pressure amplification in Wistar-Kyoto and spontaneously hypertensive rats Am J Physiol Heart Circ Physiol, May 1, 2007; 292(5): H2506 - H2512. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. M. McEniery, S. Wallace, I. S. Mackenzie, B. McDonnell, Yasmin, D. E. Newby, J. R. Cockcroft, and I. B. Wilkinson Endothelial Function Is Associated With Pulse Pressure, Pulse Wave Velocity, and Augmentation Index in Healthy Humans Hypertension, October 1, 2006; 48(4): 602 - 608. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
C. Labat, R. S. A. Cunha, P. Challande, M. E. Safar, and P. Lacolley Respective contribution of age, mean arterial pressure, and body weight on central arterial distensibility in SHR Am J Physiol Heart Circ Physiol, April 1, 2006; 290(4): H1534 - H1539. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. E. Safar and P. Laurent Pulse pressure and arterial stiffness in rats: comparison with humans Am J Physiol Heart Circ Physiol, October 1, 2003; 285(4): H1363 - H1369. [Full Text] [PDF]
|
|
|
|
 |
|
 J. A. Payne, J. F. Reckelhoff, and R. A. Khalil Role of oxidative stress in age-related reduction of NO-cGMP-mediated vascular relaxation in SHR Am J Physiol Regulatory Integrative Comp Physiol, September 1, 2003; 285(3): R542 - R551. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 Y.-J. Gao, H. Yang, K. Teoh, and R. M.K.W. Lee Detrimental effects of papaverine on the human internal thoracic artery J. Thorac. Cardiovasc. Surg., July 1, 2003; 126(1): 179 - 185. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 A. Lerman and J. Herrmann Endothelial function under pressure J. Am. Coll. Cardiol., May 21, 2003; 41(10): 1759 - 1760. [Full Text] [PDF]
|
|
|
|
 |
|
 M. M. Engler, M. B. Engler, D. M. Pierson, L. B. Molteni, and A. Molteni Effects of Docosahexaenoic Acid on Vascular Pathology and Reactivity in Hypertension Experimental Biology and Medicine, March 1, 2003; 228(3): 299 - 307. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. Behr-Roussel, P. Chamiot-Clerc, J. Bernabe, K. Mevel, L. Alexandre, M. E. Safar, and F. Giuliano Erectile dysfunction in spontaneously hypertensive rats: pathophysiological mechanisms Am J Physiol Regulatory Integrative Comp Physiol, March 1, 2003; 284(3): R682 - R688. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
M. Safar, P. Chamiot-Clerc, G. Dagher, and J. F. Renaud Pulse Pressure, Endothelium Function, and Arterial Stiffness in Spontaneously Hypertensive Rats Hypertension, December 1, 2001; 38(6): 1416 - 1421. [Abstract] [Full Text] [PDF]
|
|
|
|
|
|
D. Susic, J. Varagic, and E. D. Frohlich Isolated Systolic Hypertension in Elderly WKY Is Reversed With L-Arginine and ACE Inhibition Hypertension, December 1, 2001; 38(6): 1422 - 1426. [Abstract] [Full Text] [PDF]
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||