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Research report
Autonomic and cardiovascular reflex responses to central estrogen
injection in ovariectomized female rats
*
Monique C. Saleh, Barry J. Connell, Tarek M. Saleh
Department of Anatomy and Physiology, Atlantic Veterinary College, University of Prince Edward Island, Charlottetown, P.E.I., Canada C1A 4P3 Accepted 25 July 2000
Abstract
The role of estrogen in central autonomic nuclei was examined in ovariectomized female Sprague–Dawley rats supplemented daily for 7 days with either estrogen (5mg / kg; sc) or saline (0.9%; sc). Animals were subsequently anaesthetized with sodium thiobutabarbital (Inactin; 100 mg / kg; ip) and instrumented to record blood pressure and heart rate. Efferent vagal parasympathetic (VPNA) and renal sympathetic (RSNA) nerve activities were recorded and used to assess baseline and reflexive changes in autonomic tone. The cardiac baroreflex was evoked using a single bolus injection of phenylephrine (0.1 mg / kg) both before and following either intrathecal injection of estrogen (0.5 mM; 1 ml) or bilateral injection of estrogen (0.5 mM; 100 nl / side) into several central autonomic nuclei. In estrogen-replaced rats, both the baseline and PE-evoked values for mean arterial pressure and RSNA were significantly decreased following injection of estrogen into the nucleus tractus solitarius (NTS), rostral ventrolateral medulla (RVLM), parabrachial nucleus (PBN), central nucleus of the amygdala (CNA) and the intrathecal space. Baseline heart rate and VPNA were significantly decreased following injection of estrogen into NTS, nucleus ambiguus (Amb), PBN and the intrathecal space. PE-evoked changes in heart rate and VPNA were significantly enhanced following injection of estrogen into these same nuclei. Injection of estrogen into the insular cortex (IC) produced significant decreases in baseline and PE-evoked RSNA only. The cardiac baroreflex was significantly enhanced following injection of estrogen into all nuclei and the intrathecal space. In saline-replaced females, injection of estrogen into NTS, RVLM, Amb and the intrathecal space had similar effects on both baseline and PE-evoked parameters although of a reduced magnitude compared to estrogen-replaced rats. However, no significant changes in autonomic tone and baroreflex function were observed following the injection of estrogen into the PBN, CNA or IC of saline-replaced rats. These results demonstrate a role for estrogen in central autonomic nuclei in female rats and suggest a possible alteration of estrogen receptor distribution or efficacy within the central nervous system of estrogen-deficient female rats. 2000 Elsevier Science B.V. All rights reserved.
Theme: Endocrine and autonomic regulation
Topic: Cardiovascular regulation
Keywords: Parabrachial nucleus; Central nucleus of the amygdala; Insular cortex; Nucleus ambiguus; Nucleus tractus solitarius; Rostral ventrolateral medulla; Spinal cord
1. Introduction nucleus ambiguus and intermediolateral cell column of the
spinal cord respectively [18,19]. With the additional evi-There is increasing evidence to support a role for dence of estrogen receptor mRNA [1,22,23] as well as the estrogen as a central modulator of autonomic tone. Experi- estrogen-synthesizing enzyme, aromatase cytochrome P-ments in male and female rats have demonstrated that 450 within discrete regions of the central nervous system intravenous estrogen administration produces significant [16], the contribution of locally-produced estrogen to the changes in autonomic tone via direct effects on para- regulation of autonomic and cardiovascular reflexes be-sympathetic and be-sympathetic preganglionic neurons in the comes more likely.
Experiments in male rats have demonstrated that direct injection of estrogen into cardiovascular and autonomic
*Corresponding author. Tel.: 11-902-566-0819; fax: 1
1-902-566-nuclei in the brain stem elicits significant changes in
0832.
E-mail address: [email protected] (T.M. Saleh). autonomic tone and baroreflex function [20]. Specifically,
significant increases in parasympathetic tone and barorefl- daily subcutaneous injections of either estrogen (17b -ex sensitivity were observed following bilateral injection estradiol-3-sulfate, water soluble form; 5 mg / kg; Sigma of estrogen into the nucleus tractus solitarius and nucleus Chemical, St. Louis, MO, USA; n555) or physiological ambiguus. Conversely, sympathetic tone was significantly saline (0.9%; n553) over an additional 7 days. This decreased following injection of estrogen into the nucleus estrogen replacement regimen produces sustained serum tractus solitarius and rostral ventrolateral medulla [20]. In estrogen levels similar to that in an intact rat during general, the apparent role of estrogen in cardiovascular proestrous (40–50 pg / ml) [19].
nuclei is to produce a shift in sympatho-vagal balance On the day of experimentation, animals were anaesthet-toward the parasympathetic limb resulting in an enhance- ized with sodium thiobutabarbital (Inactin; RBI, Natick, ment of baroreflex function which has been shown to MA, USA; 100 mg / kg; ip) and instrumented to record provide antifibrillatory protection on the heart [5]. blood pressure, heart rate and efferent vagal and renal Investigation into the role of estrogen in cardiovascular nerve activities as described previously [17–19]. Blood nuclei of female rats has been limited. In estrogen-replaced pressure and heart rate data were displayed and analysed ovariectomized female rats, the cardiovascular responses to using POLYVIEW PRO/ 32 data acquisition software (Grass;
glutamate injection in the bed nucleus of the stria ter- Warwick, RI, USA). The multi-unit nerve activity was minalis were significantly enhanced when preceded by amplified by a Grass model P55 preamplifier (Grass) with injection of estrogen [6]. Similar injections of estrogen in a 100-Hz to 3-kHz bandpass and 60-Hz notch filter and non-estrogen replaced ovariectomized female rats had no then displayed using thePOLYVIEW PRO/ 32 data acquisition
effect on the glutamate-evoked responses [6] suggesting system (Grass). A sampling rate of 2000 / s was used to that the effects of estrogen within the central nervous record the raw nerve signal. Non-biological noise was system may in fact be dependent on levels of circulating obtained by recording from the nerve after death and was estrogen in the peripheral vasculature. The present in- subtracted from the nerve signal recorded during the vestigation will attempt to expand our understanding of the experiment. A venous catheter (PE-10) was inserted into role of estrogen within the central nervous system as well the right femoral vein to permit administration of drugs. as the contribution of peripheral estrogen levels to the Respiration was facilitated via the insertion of an endotra-neuromodulatory function of estrogen. Specifically, the cheal tube and ventilation with room air on a Harvard effects of estrogen injection into several central autonomic rodent ventilator (65 strokes per min; 2.5-ml tidal volume). nuclei on autonomic tone and baroreflex function will be
examined in estrogen-replaced and saline-replaced ovariec- 2.2. Central injections tomized female rats. Changes in autonomic tone will be
assessed by monitoring efferent vagal and renal nerve Animals (n593) were placed in a David Kopf (Tujunga, activities. Baroreflex function will be assessed using CA, USA) stereotaxic frame and small burr holes were intravenous administration of a single dose of phenylep- drilled bilaterally through the skull to permit stereotaxic hrine hydrochloride. Finally, co-injection of a potent and insertion of a 30-gauge stainless steel, 1-ml Hamilton selective estrogen receptor antagonist, ICI 182,780 [10,25], micro-syringe. A bilateral injection of either estrogen with estrogen into brain nuclei will be used to verify the (17b-estradiol-3-sulphate; Sigma-Aldrich; St. Louis, MO, specificity and receptor-mediated action of estrogen on USA; 0.5 mM; 100 nl per side) or a combination of autonomic tone and baroreflex function. estrogen (0.5mM) and ICI 182,780 (Tocris; Bristol, UK; 1 pM; 100 nl per side) was made into each of the following nuclei according to coordinates obtained from a stereotaxic
2. Materials and methods atlas of the rat brain [15]: nucleus tractus solitarius (NTS),
nucleus ambiguus (Amb), rostral ventrolateral medulla All experiments were carried out in accordance with the (RVLM), parabrachial nucleus (PBN), central nucleus of guidelines of the Canadian Council on Animal Care and the amygdala (CNA) and insular cortex (IC). Control were approved by the University of Prince Edward Island injections of physiological saline (0.9%; 100 nl per side) Animal Care Committee. and ICI 182,780 were made into each nucleus prior to injection of estrogen and ICI 182,780 / estrogen
respective-2.1. General surgical procedures ly.
Experiments were performed on a total of 108 female 2.3. Intrathecal injections Sprague–Dawley rats (Charles Rivers; Montreal, PQ)
membrane. The catheter was advanced caudally through Changes in nerve activity and phenylephrine-induced the subarachnoid space placing the tip of the catheter cardiovascular responses were analysed by two-way immediately rostral to the lumbar enlargement (T ) To12 . ANOVA for repeated measures followed by a Student– inject, the catheter was slowly withdrawn over a distance Newman–Keul’s post hoc analysis (Sigma Stat). In all of 5 cm while making 200-nl injections at 1-cm intervals cases, differences were considered significant if P#0.05. between the lumbar enlargement (T ) and the base of the12
cervical spinal cord (T ) Control injections of saline1 . 2.6. Histology (0.9%; 1 ml) preceded intrathecal estrogen injection.
Control injections of saline / ICI 182,780 (0.9%; 1 pM; 1 At the end of each experiment animals were perfused ml) preceded intrathecal injection of estrogen / ICI 182,780. transcardially with 0.9% saline followed by 10% formalin. The brains were removed and stored in 10% formalin until 2.4. Baroreflex testing and autonomic tone the location of micro-syringe tracks could be verified
measurements histologically in thionin-stained coronal sections (6100
mm). For verification of intrathecal catheter placement, 1 In all animals, the baroreflex was evoked by the ml of blue ink was injected using the protocol described intravenous administration of phenylephrine hydrochloride above and the presence of ink in the region of the base of (PE; 0.1 mg / kg) 5 min prior to, and 5, 30, 60, 90 and 120 the cervical spinal cord (T ) to the rostral tip of the lumbar1 min following the central injection of estrogen and 5 min enlargement (T ) was confirmed.12
prior to, and 5, 30, and 60 min following the central injection of estrogen / ICI 182, 780. As well, the baroreflex
was tested 5 min prior to and 5 and 30 min following 3. Results
control injections of saline and ICI 182,780.
Sympatho-vagal balance was assessed at each time point by moni- 3.1. Effect of estrogen on baseline parameters toring changes in renal and vagal efferent nerve activities,
as well as by calculating the ratio of the bradycardic 3.1.1. Estrogen-replaced animals
response to the phenylephrine-evoked pressor response Prior to estrogen injection, mean arterial pressure (Index of Baroreflex Function5DHR /DMAP beats per (MAP) and heart rate (HR) were 100612 mmHg and
min / mmHg). 298619 beats per min respectively (n555). Baseline
values for vagal parasympathetic nerve activity (VPNA) 2.5. Data analysis and renal sympathetic nerve activity (RSNA) were 1964 mV (n555) and 1565 mV (n555) respectively. Control All data are presented as mean6standard error of the injections of saline and co-injection of estrogen / ICI mean (S.E.M.). Changes in blood pressure, heart rate and 182,780 into all nuclei and the intrathecal space had no nerve activity data were calculated at pertinent time points effect on baseline blood pressure, heart rate or nerve using the analysis mode of the POLYVIEW PRO/ 32 software activities (data not shown). Baseline mean arterial pressure
program. Changes in blood pressure and heart rate were and RSNA were significantly decreased 30 min following analysed by a one-way analysis of variance (ANOVA) for injection of estrogen into NTS (n54), RVLM (n54), PBN repeated measures followed by a Student–Newman– (n54), CNA (n54) and the intrathecal space (n53; Table Keul’s post hoc analysis (Sigma Stat, Jandel Scientific). 1). Injection of estrogen into the IC (n54) produced a
Table 1
Effect of estrogen injection in central autonomic nuclei on baseline parameters
Injection site DMAP (mmHg) DHR (bpm) DVPNA (%) DRSNA (%)
significant decrease in RSNA only (Table 1). Baseline heart rate was significantly decreased and VPNA was heart rate was significantly decreased and VPNA was significantly increased at 5 min post-estrogen injection into significantly increased at 5 min post-estrogen injection into NTS, Amb (n54) and the intrathecal space (Table 1). All NTS, Amb (n54), PBN and the intrathecal space (Table baseline parameters returned to pre-injection values 60 min 1). All baseline parameters returned to pre-injection values post-estrogen injection. Injection of estrogen into PBN 60 min post-estrogen injection. (n54), CNA (n54) and IC (n54) had no significant effect
on MAP, HR, VPNA or RSNA (Table 1). 3.1.2. Saline-replaced animals
Prior to estrogen injection mean arterial pressure (MAP) 3.2. Effect of estrogen on baroreflex function and heart rate (HR) were 111615 mmHg and 329622
beats per min respectively (n553) which were signifi- 3.2.1. Estrogen-replaced animals
cantly elevated compared to estrogen-replaced animals Testing of the baroreflex with phenylephrine (PE) prior (P,0.05). Baseline values for vagal parasympathetic nerve to central injection of estrogen evoked an increase in MAP activity (VPNA) and renal sympathetic nerve activity (1762 mmHg; n555) accompanied by a reflexive de-(RSNA) were 1663 mV (n553) and 1865 mV (n553) crease in HR (21162 beats per min; n555; Figs. 1A and respectively. Control injections of saline and co-injection 2A). As well, during baroreflex testing VPNA was in-of estrogen / ICI 182,780 into all nuclei and the intrathecal creased 45610% (n555) and RSNA was decreased space had no effect on baseline blood pressure, heart rate 2668% (n555) relative to baseline levels (Fig. 1A). The or nerve activities (data not shown). Baseline mean arterial index of baroreflex function at this time point was pressure and RSNA were significantly decreased 30 min 0.760.05 beats per min / mmHg (n555; Fig. 4A). RSNA following injection of estrogen into NTS (n54), RVLM and the pressor response to PE were significantly at-(n54) and the intrathecal space (n54; Table 1). Baseline tenuated 30 min following injection of estrogen into NTS
Fig. 2. Mean changes from baseline in mean arterial pressure (MAP) and heart rate (HR) in response to phenylephrine injection (0.1 mg / kg; i.v.) before and following central injection of saline (0.9%, control) or estrogen (0.5mM; 100 nl per side; estrogen) in estrogen-replaced (A) or saline-replaced (B) ovariectomized female rats. Asterisks indicate significance (P,0.05; ANOVA) from pre-injection value (before). NTS, nucleus tractus solitarius; Amb, nucleus ambiguus; RVLM, rostral ventrolateral medulla; PBN, parabrachial nucleus; CNA, central nucleus of the amygdala; IC, insular cortex; i.t., intrathecal space of the spinal cord.
Fig. 3. Mean changes in vagal (VPNA) and renal (RSNA) efferent nerve activities given as a per cent change from baseline (0%) in response to phenylephrine injection (0.1 mg / kg; i.v.) following central injection of saline (0.9%, control) or estrogen (0.5mM; estrogen) in estrogen-replaced (A) or saline-replaced (B) ovariectomized female rats. Asterisks indicate significance (P,0.05; ANOVA) from pre-injection value (before). NTS, nucleus tractus solitarius; Amb, nucleus ambiguus; RVLM, rostral ventrolateral medulla; PBN, parabrachial nucleus; CNA, central nucleus of the amygdala; IC, insular cortex; i.t., intrathecal space of the spinal cord.
MAP, HR, VPNA and RSNA returned to pre-injection unilateral or outside the intended region produced no values 90 min post-estrogen injection. Injection of estrogen significant effects on baseline parameters nor on PE-into PBN (n54), CNA (n54) and IC (n54) had no evoked changes in the same parameters (data not shown). significant effect on the PE-evoked changes in MAP, HR, As well, the sites of injection for saline and ICI 182,780 VPNA or RSNA (Figs. 2B and 3B). controls have been omitted from Figs. 5 and 6 for clarity.
3.3. Histological verification of cannulae placement
4. Discussion
Figs. 5 and 6 are composite diagrams indicating the
Fig. 4. Effect of central estrogen (0.5 mM; 100 nl / side; estrogen) injection on baroreflex function in estrogen-replaced (A) and saline-replaced (B) ovariectomized female rats. Index of baroreflex function given as a ratio of the peak change in heart rate to blood pressure in response to a single dose of phenylephrine (0.1 mg / kg; i.v.). Control injections of saline (0.9%; control) had no effect on baroreflex function. Asterisks indicate significance (P,0.05; ANOVA) from pre-injection value (before). NTS, nucleus tractus solitarius; Amb, nucleus ambiguus; RVLM, rostral ventrolateral medulla; PBN, parabrachial nucleus; CNA, central nucleus of the amygdala; IC, insular cortex; i.t., intrathecal space of the spinal cord.
cardiovascular autonomic reflexes. These findings are 4.1. Estrogen receptors in the CNS consistent with similar experiments in male rats [20] with
(i.e. Amb.) or indirectly by an attenuation of sympathetic output at the level of the brain stem (RVLM) or spinal cord [18]. In addition, injection of estrogen into forebrain and midbrain nuclei suggests a possible role for estrogen as a modulator of ascending and / or descending car-diovascular and autonomic information.
4.2. Estrogen vs. saline-replaced female rats
Co-injection of estrogen with the estrogen receptor antagonist ICI 182,780 provides confirmation that the changes in autonomic tone and cardiovascular reflex function observed following estrogen injection are in fact mediated by the activation of estrogen receptors. With this assumption, it is tempting to speculate that the apparent ineffectiveness of estrogen in forebrain nuclei of saline-replaced rats was due to an absence of estrogen receptors. In situ hybridization studies have demonstrated a correla-tion between estrogen receptor mRNA in the hypothalamus and serum estrogen levels in ovariectomized dogs and rats [21,24]. Specifically, estrogen receptor mRNA was found to be very low in the ovariectomized dog or rat and significantly increased following exogenous estrogen ad-ministration [21,24]. The functional significance of these findings remains unclear and warrants further investiga-tion. However, if estrogen receptor populations are in fact down-regulated in response to decreased serum estrogen levels, results in this study would suggest a progressive loss of receptors originating in the forebrain and proceed-ing towards the brain stem.
Another scenario which may be entertained is that of an accelerated clearance or inactivation of estrogen in fore-brain nuclei of saline-replaced female rats. There is evidence to suggest that steroid hormones are rendered
Fig. 5. Serial schematic diagram of coronal sections (6100mm) of the
inactive when sulfated and returned to a bioactive form in
rat brain depicting the approximate placement of microinjection cannulae
the presence of a sulphatase enzyme [9]. Estrone sulfatase
within brain stem nuclei. (A) Rostral ventrolateral medulla (RVLM) and
nucleus ambiguus (Amb). (B) Nucleus tractus solitarius (NTS). Numbers activity has been demonstrated in several tissues including on the right indicate distance from bregma in mm [15]. Injection sites are brain [9], however investigation into the correlation be-depicted unilaterally for purposes of clarity. Open circles represent sites
tween estrone sulfatase activity and serum estrogen levels
of estrogen injection which produced significant changes in either
has been limited to studies involving tissue homogenates
cardiovascular parameters or autonomic tone during baroreflex testing.
from brain and pituitary [2]. The authors found estrone
Closed circles represent sites of estrogen / ICI 182,780 injection in which
phenylephrine-induced changes in cardiovascular parameters and au- sulphatase activity to be two-fold higher in the anterior tonomic tone were not significantly different from pre-injection values. pituitary of intact females compared to ovariectomized Both saline and ICI 182,780 control injection sites have been omitted
female or male rats suggesting that normal female rats are
from the figure for clarity. 12, hypoglossal nucleus; Amb, nucleus
exposed to a larger pool of estrogen in its bioactive form
ambiguus; AP, area postrema; cc, corpus callosum; LPGi, lateral
while ovariectomized females and males possess greater
paragigantocellular nucleus; NTS, nucleus tractus solitarius; py,
pyrami-dal tract; ROb, raphe obscurus nucleus; RVLM, rostral ventrolateral quantities of estrogen in an inactive form. No such nucleus; Sp5C, spinal trigeminal nucleus, caudal part; Sp5I, spinal correlation was observed between serum estrogen levels trigeminal nucleus, interpolar part.
Fig. 6. Serial schematic diagram of coronal sections (6100mm) of the rat brain depicting the approximate placement of microinjection cannulae within the (A) insular cortex (IC), (B) central nucleus of the amygdala (CNA) and (C) parabrachial nucleus (PBN). Numbers on the right indicate distance from bregma in mm [15]. Injection sites are depicted unilaterally for purposes of clarity. Open circles represent sites of estrogen injection which produced significant changes in either cardiovascular parameters or autonomic tone during baroreflex testing. Closed circles represent sites of estrogen / ICI 182,780 injection in which phenylephrine-induced changes in cardiovascular parameters and autonomic tone were not significantly different from pre-injection values. Both saline and ICI 182,780 control injection sites have been omitted from the figure for clarity. 4V, fourth ventricle; BL, basolateral amygdaloid nucleus; CA3, field CA3 of Ammon’s horn; cc, corpus callosum; CNA, central amygdaloid nucleus; CPu, caudate putamen; IC, insular cortex; Ic, internal capsule; LH, lateral hypothalamic area; PBN, parabrachial nucleus; py, pyramidal tract; Sp5O, spinal trigeminal nerve, oral part.
sion and neuropeptidergic characterization of estrogen receptors
included in this study. Further investigation into the
(ERa and ERb) throughout the rat brain: anatomical evidence of
conditions under which estrogen is released into central
distinct roles of each subtype, J. Neurobiol. 36 (1998) 357–378.
nuclei will provide valuable insight into the role of this [12] L. Leduc, N. Wasserstrum, T. Spillman, D.B. Cotton, Baroreflex hormone in central cardiovascular regulation. function in normal pregnancy, Am. J. Obstet. Gynecol. 165 (1991)
886–890.
[13] A.D. Loewy, K.M. Spyer, Central autonomic pathways, in: A.D. Loewy, K.M. Spyer (Eds.), Central Regulation of Autonomic
Acknowledgements
Function, Oxford University Press, New York, 1990, pp. 88–103. [14] C.T. Minson, J.R. Halliwill, T.M. Young, M.J. Joyner, Influence of
This works was funded by a grant ([615122) from the the menstrual cycle on sympathetic activity, baroreflex sensitivity,
Heart and Stroke Foundation of Prince Edward Island. and vascular transduction in young women, Circulation 101 (2000) 862–868.
[15] G. Paxinos, C. Watson, The Rat Brain in Stereotaxic Coordinates, Academic Press, New York, 1986.
References [16] C.E. Roselli, S.E. Abdelgadir, O.K. Ronnekleiv, S.A. Klosterman,
Anatomic distribution and regulation of aromatase gene expression [1] A. Amundesson, O. Hermanson, A. Blomqvist, Estrogen receptor- in the rat brain, Biol. Reprod. 58 (1998) 79–87.
like immunoreactivity in the medullary and spinal dorsal horn of the [17] T.M. Saleh, B.J. Connell, Role of 17b-estradiol in the modulation of female rat, Neurosci. Lett. 196 (1996) 25–28. baroreflex sensitivity in male rats, Am. J. Physiol. 275 (1998) [2] P.B. Connolly, J.A. Resko, Estrone sulphatase activity in rat brain R770–R778.
and pituitary: effects of gonadectomy and the estrous cycle, J. [18] T.M. Saleh, B.J. Connell, Centrally mediated effect of 17b-estradiol Steroid Biochem. 33 (1989) 1013–1018. on parasympathetic tone in male rats, Am. J. Physiol. 276 (1999) [3] K.P. Corodimas, J.I. Morrell, Estradiol-concentrating forebrain and R474–R481.
midbrain neurons project directly to the medulla, J. Comp. Neurol. [19] T.M. Saleh, B.J. Connell, 17b-estradiol modulates baroreflex sen-291 (1990) 609–620. sitivity and autonomic tone of female rats, J. Autonom. Nerv. Syst. [4] M. El-Mas, A.A. Abdel-Rahman, Estrogen enhances baroreflex 80 (2000) 148–161.
control of heart rate in conscious ovariectomized rats, Can. J. [20] M.C. Saleh, T.M. Saleh, B.J. Connell, 17b-estradiol modulates Physiol. Pharmacol. 76 (1998) 381–386. baroreflex sensitivity and autonomic tone in the brainstem and spinal [5] M. Esler, The autonomic nervous system and cardiac arrhythmias, cord of male rats, Brain Res. 867 (2000) 200–209.
Clin. Auton. Res. 2 (1992) 33–135. [21] P.J. Shughrue, C.D. Bushnell, D.M. Dorsa, Estrogen receptor mRNA [6] L.N. Gibbons, J. Ciriello, Effect of oestrogen on the cardiovascular in female rat brain during the estrous cycle: a comparison with responses to glutamate stimulation of bed nucleus of the stria ovariectomized females and intact males, Endocrinology 131 (1992) terminalis, Fundam. Clin. Pharmacol. 11 (1997) 105s–108s. 381–388.
[7] X. He, W. Wang, J.T. Crofton, L. Share, Effects of 17b-estradiol on [22] P.J. Shughrue, L.V. Lane, I. Merchenthaler, Comparative distribution sympathetic activity and pressor response to phenylephrine in of estrogen receptor-a and -b mRNA in the rat central nervous ovariectomized rats, Am. J. Physiol. 275 (1998) R1202–R1208. system, J. Comp. Neurol. 388 (1997) 507–525.
[8] X. He, W. Wang, J.T. Crofton, L. Share, Effects of 17b-estradiol on [23] R.B. Simerly, C. Chang, M. Muramatsu, L.W. Swanson, Distribution the baroreflex control of sympathetic activity in conscious ovariec- of androgen and estrogen receptor mRNA-containing cells in the rat tomized rats, Am. J. Physiol. 277 (1999) R493–R498. brain: an in situ hybridization study, J. Comp. Neurol. 294 (1990) [9] R. Hobrick, Steroid sulphotransferases and steroid sulphate sulfat- 76–95.
ases: characteristics and biological roles, Can. J. Biochem. Cell Biol. [24] H. Tani, T. Inaba, S. Matsuyama, Y. Takamori, T. Sawada, Enhance-63 (1985) 1127–1144. ment of estrogen receptor gene expression in the mediobasal [10] S.M. Hyder, C. Chiappetta, L. Murthy, G.M. Stancel, Selective hypothalamus during anestrus in the beagle bitch, Neurosci. Lett.
inhibition of estrogen-regulated gene expression in vivo by the pure 227 (1997) 149–152.
