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Am J Physiol Regul Integr Comp Physiol 289: R1724-R1728, 2005. First published August 25, 2005; doi:10.1152/ajpregu.00468.2005
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WATER AND ELECTROLYTE HOMEOSTASIS

Influence of estradiol on micturition thresholds in the rat: involvement of the hypogastric nerve

Natalia Dmitrieva and Karen J. Berkley

Program in Neuroscience, Florida State University, Tallahassee, Florida

Submitted 30 June 2005 ; accepted in final form 12 August 2005


   ABSTRACT
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METHODS
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Studies have shown that the severity of bladder hyperreflexia induced by acute bladder inflammation varies with the ovarian cycle. These results suggest that the hyperreflexia is modulated by ovarian hormones. Other studies have suggested that such modulation involves the bladder's sympathetic innervation. These hypotheses were tested by assessing the development of bladder hyperreflexia in urethane-anesthetized rats subjected to different hormonal manipulations with or without bilateral hypogastric neurectomy (HYPX). The groups included sham ovariectomy (sham OVX), ovariectomy (OVX), OVX with estradiol replacement (OVX+E), OVX+HYPX, and OVX+HYPX+E. Assessments were performed using repeated cystometrograms (CMGs) to measure micturition thresholds (MT) before and hourly for 3 h after intravesicular treatment with 50% turpentine oil (or olive oil in an OVX+E control group). In the uninflamed bladder, treatment with estradiol increased MTs in the OVX+E group compared with the OVX group. As expected, bladder inflammation induced bladder hyperreflexia in sham OVX rats (studied in estrus). This hyperreflexia was eliminated by OVX and restored by either estradiol replacement or HYPX. Combining estradiol replacement and HYPX (i.e., OVX+E+HYPX) did not increase the severity of bladder hyperreflexia compared with either manipulation alone. These results indicate that the bladder hyperreflexia that is induced by bladder inflammation requires the presence of estradiol and suggest that this hormonal modulation is exerted via the sympathetic control of the bladder, possibly via an increase of {beta}-adrenergic inhibitory actions on the detrusor muscle. Similar mechanisms may contribute to bladder disorders in postmenopausal women.

inflammation; lower urinary tract; ovariectomy

ALTHOUGH BLADDER REFLEXES in healthy women remain stable across the menstrual cycle (37), symptoms and signs of bladder dysfunction are exacerbated perimenstrually (13, 33). Thus it appears that the rapid changes in ovarian hormones that occur perimenstrually can increase the severity of symptoms and signs of bladder dysfunction. This conclusion is consistent with findings that suppression of the menstrual cycle can alleviate symptoms (17).

The situation is somewhat different for postmenopausal women, whose bladders and urethras exhibit a loss of estrogen but not progesterone receptors (26). About one-third of postmenopausal women develop overactive bladder (25). Although it remains uncertain whether the loss of bladder and urethral estrogen receptors and reduction in plasma estrogens in postmenopausal women underlies their bladder overactivity, the conclusion is partially supported by the fact that estrogen treatment, particularly if delivered intravaginally rather than systemically, can alleviate symptoms (12, 23, 25, 27, 34).

These clinical findings indicate that the hormonal milieu influences bladder function. Evidence from animal research provides further support. In rodents as in women, bladder reflexes of the healthy bladder do not vary with the estrous cycle (8, 15). On the other hand, the severity of bladder hyperreflexia induced by bladder inflammation does vary, being more severe in association with the rapid hormonal changes during the periovulatory period (proestrus/estrus) than in other stages of the cycle (metestrus/diestrus; Ref. 15).

Loss of ovarian hormones produced by ovariectomy (OVX) and estrogen replacement (OVX+E) in the rat produce distinct effects on bladder and urethral reflex activity (31). Depending on age, these manipulations also affect responses of the detrusor muscle to cholinergic stimulation (4). Furthermore, OVX+E increases water consumption and micturition volumes but not micturition frequency (19). In mice lacking either one or both estrogen receptor subtypes compared with wild types, there are no strain differences in urodynamic parameters in healthy bladders; but after treatment of the bladder with capsaicin, signs of bladder hyperreflexia fail to appear in mice lacking estrogen receptor-{alpha} (29).

Together, these results indicate that reproductive status and hormonal milieu exert potent influences on lower urinary tract function and on responses of the bladder to pathophysiology in both women and experimental animals. In particular, they suggest that loss (or suppression) of estrogens masks and the presence of estrogens increases the bladder's vulnerability to inflammation-induced bladder hyperreflexia.

The means by which these reproductive and hormonal influences occur are poorly understood. One possibility is that regulation of detrusor activity by the hypogastric nerve is involved. Studies have shown that activation of the hypogastric nerve inhibits the detrusor muscle (3) and that acute hypogastric neurectomy (HYPX) increases motility of the healthy bladder (6). Furthermore, relaxation of the detrusor muscle by {beta}3-adrenergic agents, whose major source is the hypogastric nerve (3, 24), is increased by hormonal manipulations such as OVX and decreased by OVX+E (21, 32, 40). Estrogen treatment influences hypogastric nerve actions on the bladder (28).

It is therefore possible that when the bladder is inflamed, the presence of sufficient estradiol levels reduces the hypogastric nerve's inhibition of detrusor reflexes and that depletion of estradiol augments the inhibition. The present study tested this hypothesis in urethane-anesthetized rats by assessing the influence of OVX and OVX+E with or without HYPX on volume voiding thresholds (micturition thresholds, MTs) measured using cystometry before and after bladder inflammation with intravesicular turpentine (7, 22). If the hypothesis is correct, OVX should reduce the severity of inflammation-induced bladder hyperreflexia only when the hypogastric nerve is intact, and estradiol replacement should prevent this effect.


   METHODS
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Animals. Adult female Sprague-Dawley rats weighing 250–300 g were used. They were individually housed in chip-bedded plastic cages and maintained on a 12:12-h light-dark cycle. Each rat's reproductive status was assessed by daily vaginal smears for at least 3 wk before the experiment. Estrous stage was defined using the traditional stage assessment protocol (see Fig. 3 in Ref. 2). The study was approved by Florida State University's Institutional Animal Care and Use Committee.

Experimental groups. Seven to 10 days before the day of the experiment, rats that had exhibited at least two regular 4-day estrous cycles were subjected to OVX, sham OVX, or OVX+E. Some rats in the OVX and OVX+E groups also underwent HYPX performed as described previously by Temple et al. (36). During the experiment, the bladder was treated with either turpentine (inflammation) or olive oil. These preparations resulted in six experimental groups of 8–13 rats/group: 1) sham OVX, bladder inflammation; 2) OVX only, bladder inflammation; 3) OVX + HYPX, bladder inflammation; 4) OVX+E, bladder inflammation; 5) OVX+E+HYPX, bladder inflammation; and 6) OVX+E, olive oil treatment.

Surgical procedures for OVX, sham OVX, OVX+E, and HYPX rats. Rats were anesthetized intraperitoneally with ketamine and xylazine anesthesia (73 and 9 mg/kg, respectively). A ventral midline incision was made to expose the ovaries, which were then removed (OVX) or identified and left in place (sham OVX). In some OVX rats, a silastic capsule (Dow Corning, Midland, MI) filled with 17{beta}-estradiol was inserted subcutaneously into the nape of the neck. The capsule was 5 mm in length with a 1.57-mm internal diameter. Capsules of this size have been shown to maintain a steady ~50–60 pg/ ml 17{beta}-estradiol plasma level (18). In some OVX and OVX+E rats, the left and right hypogastric nerves were identified as they exited the inferior mesenteric ganglion, and a 5-mm section of each nerve was cut out. The abdominal incision was then sutured in layers. Hormonal status was verified by daily vaginal smears after the surgery. OVX rats produced a continued daily presence of leukocytes (diestrus-like smear pattern); OVX+E rats produced a continuous presence of cornified cells (estrus-like smear pattern); in sham OVX rats, the 4-day cyclical pattern did not change.

Cystometrograms. MTs were measured by obtaining repetitive cystometrograms (CMGs) before and after treatment of the bladder with turpentine or olive oil. The methods have been described in detail elsewhere (5). Briefly, on the day of the experiment, the rats were anesthetized with urethane (1.2 g/kg intraperitoneal injection). Rats in the group that cycled (sham OVX) were studied on the day of estrus. Body temperature was maintained at ~37°C throughout the experiment using a heating pad and warming lamp. The bladder was catheterized transurethrally with polyethylene tubing (outer diameter, 0.97 mm) with the tip placed within the lumen so that it did not touch the bladder wall. A suture was tied around the surrounding skin to prevent leakage. An abdominal incision was made in the lower abdomen to expose the bladder so that it could be emptied by gentle pressure and suction (using a cotton wick placed in the open end of the catheter) before each CMG was obtained. The incision was covered by a gauze pad soaked in warm saline. The catheter was connected to a small-volume pressure transducer whose signals were amplified and relayed to strip chart and videotape recorders for offline analyses.

Each CMG was obtained by slowly filling the bladder (0.055 ml/min). The MT was defined as the intraluminal volume that produced the first micturition contraction.

Two or three CMGs obtained at 10-min intervals were run to establish a baseline MT, and then the bladder was filled with 0.7 ml of 50% turpentine oil (in olive oil) or olive oil. The bladder was emptied 1 h later, and the first posttreatment CMG was obtained. CMGs were then obtained twice more at hourly intervals.

Data analyses. Comparisons of the effects of the various manipulations on baseline MTs were assessed using one-way ANOVA. When significant, ANOVA were followed by Bonferroni post hoc tests. Differences in MTs before and after turpentine or olive oil treatment were analyzed using repeated-measures ANOVA followed, as appropriate, by Bonferroni post hoc tests. Significance was set at P < 0.05.


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Uninflamed bladder (baseline). MTs in the sham OVX group (run in estrus) were similar to those reported previously in intact, normally cycling rats in estrus (15). As shown in the comparison of baseline MTs among four groups in Figs. 1A and 2A, OVX had no influence on MTs of the uninflamed bladder compared with the sham OVX condition. In contrast, OVX+E rats demonstrated significantly increased MTs compared with the OVX and OVX+HYPX groups (P < 0.05).



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  		Fig. 1. Effects of ovariectomy (OVX) with or without estradiol replacement (OVX+E) on the development of inflammation-induced bladder hyperreflexia. A: micturition thresholds (MTs) measured before and 1, 2, and 3 h after treating the bladder with turpentine (inflammation) or olive oil. *P < 0.05 compared with baseline in the OVX+E group. B: decreases in micturition thresholds (MTs) before and after inflammation as specified in A. *P < 0.05; **P < 0.01, compared with oil control; #P < 0.05, ##P < 0.01, and ###P < 0.005, compared with OVX rats.

 


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  		Fig. 2. Effects of hypogastric neurectomy (HYPX) on the development of inflammation-induced bladder hyperreflexia. A: MTs measured before and 1, 2, and 3 h after treating the bladder with turpentine. *P < 0.05, compared with baseline in OVX+E group. B: differences in the MTs before and after inflammation as specified in A. #P < 0.05, ##P < 0.01, and ###P < 0.005, compared with OVX rats.

 
Influence of OVX and OVX+E on bladder inflammation. As shown in Fig. 1, treatment of the bladder with turpentine induced a significant, progressive decrease in MTs in sham OVX rats in estrus that was similar in time course and magnitude to the decrease previously reported from regularly cycling rats in estrus (15). MTs in OVX rats, however, did not decrease significantly after turpentine treatment (Fig. 1A). As a result, the reduction in MTs in OVX rats was significantly less than that in sham OVX rats (P < 0.005) (Fig. 1B).

Estrogen replacement restored the inflammation-induced reduction in MTs to a level that did not differ significantly from that in the sham OVX group (Fig. 1, A and B).

Influence of HYPX on bladder inflammation. As shown in Fig. 2, HYPX, like estradiol replacement, restored bladder hyperreflexia in OVX rats, so that the reduction in MTs in OVX+HYPX rats did not differ significantly from that observed in sham OVX rats (Fig. 1). Combining HYPX and estradiol replacement with ovariectomy did not affect the inflammation-induced reduction in MTs produced by estradiol replacement. However, differences in MTs in OVX+E and OVX+E+HYPX rats were significantly different from those in OVX rats (P < 0.005) (Fig. 2B).

Control treatment of bladder. As expected, MTs after treatment of the bladder with olive oil did not change significantly over time (Fig. 1).


   DISCUSSION
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The present results show that treatment of the ovariectomized rat with 17{beta}-estradiol for 7–10 days increased MTs of the uninflamed bladder. The results also show that the bladder hyperreflexia that is produced by treating the bladder with turpentine (i.e., reduction in micturition thresholds) in cycling rats in estrus is eliminated after ovariectomy and restored by estrogen replacement. The results suggest that the hypogastric nerve contributes to these effects.

Uninflamed bladder. OVX has been found to decrease the responsiveness of isolated bladder muscle strips to cholinergic stimulation, to decrease maximum urine flow rate and voiding frequency, and to increase urethral opening pressure (4). These results led the authors to conclude that OVX compromises either the urethral wall musculature or urethral innervation. In the present study, we found that OVX had no effect on baseline MTs compared with regularly cycling rats. Because the intraluminal bladder pressure in the present study was measured via a transurethral catheter, the MT depended mostly on the motility of the bladder itself. Thus the influence of OVX may be less on the detrusor muscle than on urethral activity. In contrast to the lack of effects of OVX, however, estradiol replacement significantly increased baseline MTs, which is consistent with the report that estradiol increases micturition volumes compared with OVX and sham OVX rats (19). Furthermore, long-term estrogen replacement has been shown to increase bladder contractile responsiveness to carbachol compared with sham OVX rats (19). These findings are consistent with urodynamic assessments in postmenopausal women with and without estrogen replacement that indicate that estrogen replacement increases bladder sensory threshold (9).

Bladder inflammation and estradiol. Consistent with our earlier findings in regularly cycling intact rats in estrus (15), bladder inflammation in the present study induced significant bladder hyperreflexia in sham OVX rats in estrus. In the same earlier study, we also found that the severity of hyperreflexia induced by bladder inflammation decreased during the 2 days following the acute fall in ovarian hormones, that is, during metestrus and diestrus (15). This reduction is consistent with our finding in the present study that 7–10 days after OVX, inflammation-induced bladder hyperreflexia was significantly reduced.

The {beta}3-adrenoreceptor has recently been identified in the rat bladder (10). In the bladder of the rat and other species, activation of this receptor relaxes smooth muscles (10, 20, 30, 38, 39). Thus, in a rat model of bladder hyperactivity, the {beta}3-adrenoreceptor agonist CL316,243 inhibits bladder hyperreflexia and detrusor instability (38), increases micturition interval, and decreases micturition volume in rats with prostaglandin E2-induced bladder hyperreflexia (35).

Recent studies by others have shown that OVX increases the relaxant effect of a {beta}3-adrenoreceptor agonist on detrusor muscles and that estradiol replacement abolishes this increase (21, 32) Thus one possible means by which the low ovarian hormone levels that result from OVX could decrease inflammation-induced bladder hyperreflexia is via an increase in {beta}3-adrenergic activity. Because the opposite condition created by estradiol replacement restored hyperreflexia, it is possible that estradiol tonically suppresses {beta}3-adrenergic activity.

Bladder inflammation and HYPX. Similarly to OVX+E, OVX+HYPX also restored inflammation-induced bladder hyperreflexia compared with OVX alone. That HYPX added to OVX+E did not increase the hyperreflexia even further than either manipulation alone suggests that estradiol and HYPX could reinstate inflammation-induced bladder hyperreflexia in the OVX rats via the same mechanism, i.e., by decreasing {beta}3-adrenergic activity. The converse might also apply, i.e., that inflammation-induced activity in hypogastric nerve fibers relaxes the estrogen-depleted bladder by increasing {beta}3-adrenergic activity. Consistent with this possibility is that application of noradrenaline inhibits contractions of guinea pig bladder strips that are induced by stimulating the hypogastric nerve (11).

Acute activation of hypogastric nerve activity has been shown to inhibit micturition (3), while acute HYPX reduces micturition thresholds (6). It is therefore possible that the development of inflammation-induced bladder hyperreflexia involves activity in hypogastric nerve fibers, particularly sensory afferents. Thus OVX could reduce the bladder hyperreflexia induced by bladder inflammation by influencing hypogastric nerve activity. However, the fact that OVX did not reduce baseline MTs (i.e., MTs in the uninflamed bladder), an effect that one would expect if the sensitivity of the hypogastric nerve to sensory stimulation changed, is inconsistent with this possibility.

Clinical relevance. These results may be relevant to women's health. Postmenopausal women have a higher risk of urinary tract infections (14). Despite such a risk, there is evidence to suggest that the bladder in postmenopausal women may not respond to inflammation as it does in young females. Thus postmenopausal women have been found to void with weaker detrusor contractions compared with premenopausal women (16), which may at least be partly due to a decreased intramural_bladder thickness in postmenopausal women, which positively correlates with the circulating estradiol level (1). As the present results suggest, hormonal depletion may also lead to a decreased response of the bladder to bladder inflammation, possibly because of an abnormal relaxant response to hypogastric nerve activation. If so, then postmenopausal women may be at risk of having bladder inflammation go unnoticed because bladder hyperreflexia is a major problem associated with this condition.


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This study was supported by National Institute of Neurological Disorders and Stroke Grant R01-NS-11892.


   ACKNOWLEDGMENTS
 
We thank John Chalcraft for help with the figures.


   FOOTNOTES
 

Address for reprint requests and other correspondence: N. Dmitrieva, Program in Neuroscience, Florida State Univ., Copeland St., Tallahassee, FL 32306–1270 (E-mail: dmitrieva{at}psy.fsu.edu)

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.


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  1. Battaglia C, Salvatori M, Giulini S, Primavera MR, Gallinelli A, and Volpe A. Hormonal replacement therapy and urinary problems as evaluated by ultrasound and color Doppler. Ultrasound Obstet Gynecol 13: 420–424, 1999.[Medline]
  2. Becker JB, Arnold AP, Berkley KJ, Blaustein JD, Eckel LA, Hampson E, Herman JP, Marts S, Sadee W, Steiner M, Taylor J, and Young E. Strategies and methods for research on sex differences in brain and behavior. Endocrinology 146: 1650–1673, 2005.[Abstract/Free Full Text]
  3. De Groat WC and Theobald RJ. Reflex activation of sympathetic pathways to vesical smooth muscle and parasympathetic ganglia by electrical stimulation of vesical afferents. J Physiol 259: 223–237, 1976.[Abstract/Free Full Text]
  4. Diep N and Constantinou CE. Age dependent response to exogenous estrogen on micturition, contractility and cholinergic receptors of the rat bladder. Life Sci 64: PL279–PL289, 1999.[CrossRef]
  5. Dmitrieva N and Berkley KJ. Contrasting effects of WIN 55212-2 on motility of the rat bladder and uterus. J Neurosci 22: 7147–7153, 2002.[Abstract/Free Full Text]
  6. Dmitrieva N, Johnson OL, and Berkley KJ. Bladder inflammation and hypogastric neurectomy influence uterine motility in the rat. Neurosci Lett 313: 49–52, 2001.[CrossRef][ISI][Medline]
  7. Dmitrieva N, Shelton D, Rice AS, and McMahon SB. The role of nerve growth factor in a model of visceral inflammation. Neuroscience 78: 449–459, 1997.[CrossRef][ISI][Medline]
  8. Dörr W. Endogenous factors modulating urinary bladder compliance in mice. J Urol 150: 1938–1944, 1993.[Medline]
  9. Fantl JA, Wyman JF, Anderson RL, Matt DW, and Bump RC. Postmenopausal urinary incontinence: comparison between non-estrogen-supplemented and estrogen-supplemented women. Obstet Gynecol 71: 823–828, 1988.[Medline]
  10. Fujimura T, Tamura K, Tsutsumi T, Yamamoto T, Nakamura K, Koibuchi Y, Kobayashi M, and Yamaguchi O. Expression and possible functional role of the {beta}3-adrenoceptor in human and rat detrusor muscle. J Urol 161: 680–685, 1999.[CrossRef][ISI][Medline]
  11. Gillespie JI. Noradrenaline inhibits autonomous activity in the isolated guinea pig bladder. BJU Int 93: 401–409, 2004.[Medline]
  12. Hextall A. Oestrogens and lower urinary tract function. Maturitas 36: 83–92, 2000.[CrossRef][ISI][Medline]
  13. Hextall A, Bidmead J, Cardozo L, and Hooper R. The impact of the menstrual cycle on urinary symptoms and the results of urodynamic investigation. BJOG 108: 1193–1196, 2001.[Medline]
  14. Hooton TM. Recurrent urinary tract infection in women. Int J Antimicrob Agents 17: 259–268, 2001.[CrossRef][ISI][Medline]
  15. Johnson OL and Berkley KJ. Estrous influences on micturition thresholds of the female rat before and after bladder inflammation. Am J Physiol Regul Integr Comp Physiol 282: R289–R294, 2002.[Abstract/Free Full Text]
  16. Karram MM, Partoll L, Bilotta V, and Angel O. Factors affecting detrusor contraction strength during voiding in women. Obstet Gynecol 90: 723–726, 1997.[Abstract]
  17. Lentz GM, Bavendam T, Stenchever MA, Miller JL, and Smalldridge J. Hormonal manipulation in women with chronic, cyclic irritable bladder symptoms and pelvic pain. Am J Obstet Gynecol 186: 1268–1273, 2002.[Medline]
  18. Lerant A and Freeman ME. Ovarian steroids differentially regulate the expression of PRL-R in neuroendocrine dopaminergic neuron populations: a double label confocal microscopic study. Brain Res 802: 141–154, 1998.[CrossRef][ISI][Medline]
  19. Longhurst PA, Kauer J, Leggett RE, and Levin RM. The influence of ovariectomy and estradiol replacement on urinary bladder function in rats. J Urol 148: 915–919, 1992.[ISI][Medline]
  20. Longhurst PA and Levendusky M. Pharmacological characterization of {beta}-adrenoceptors mediating relaxation of the rat urinary bladder in vitro. Br J Pharmacol 127: 1744–1750, 1999.[CrossRef]
  21. Matsubara S, Okada H, Shirakawa T, Gotoh A, Kuno T, and Kamidono S. Estrogen levels influence {beta}3-adrenoceptor-mediated relaxation of the female rat detrusor muscle. Urology 59: 621–625, 2002.[CrossRef][Medline]
  22. McMahon SB and Abel C. A model for the study of visceral pain states: chronic inflammation of the chronic decerebrate rat urinary bladder by irritant chemicals. Pain 28: 109–127, 1987.[CrossRef][ISI][Medline]
  23. Miodrag A, Castleden CM, and Vallance TR. Sex hormones and the female urinary tract. Drugs 36: 491–504, 1988.[ISI][Medline]
  24. Morrison JFB. Reflex control of the lower urinary tract. In: The Physiology of the Lower Urinary Tract, edited by Torrens M and Morrison JFB. London, UK: Springer, 1987, p. 193–235.
  25. Ouslander JG. Management of overactive bladder. N Engl J Med 350: 786–799, 2004.[Free Full Text]
  26. Rizk DE, Raaschou T, Mason N, and Berg B. Evidence of progesterone receptors in the mucosa of the urinary bladder. Scand J Urol Nephrol 35: 305–309, 2001.[Medline]
  27. Rufford J, Hextall A, Cardozo L, and Khullar V. A double-blind placebo-controlled trial on the effects of 25 mg estradiol implants on the urge syndrome in postmenopausal women. Int Urogynecol J Pelvic Floor Dysfunct 14: 78–83, 2003.[Medline]
  28. Sato S, Hayashi RH, and Garfield RE. Mechanical responses of the rat uterus, cervix, and bladder to stimulation of hypogastric and pelvic nerves in vivo. Biol Reprod 40: 209–219, 1989.[Abstract]
  29. Schroder A, Pandita RK, Hedlund P, Warner M, Gustafsson JA, and Andersson KE. Estrogen receptor subtypes and afferent signaling in the bladder. J Urol 170: 1013–1016, 2003.[CrossRef][Medline]
  30. Seguchi H, Nishimura J, Zhou Y, Niiro N, Kumazawa J, and Kanaide H. Expression of {beta}3-adrenoceptors in rat detrusor smooth muscle. J Urol 159: 2197–2201, 1998.[CrossRef][Medline]
  31. Seidlová-Wuttke D, Schultens A, Jarry H, and Wuttke W. Urodynamic effects of estradiol (E2) in ovariectomized (ovx) rats. Endocrine 23: 25–32, 2004.[Medline]
  32. Shenfeld OZ, McCammon KA, Blackmore PF, and Ratz PH. Rapid effects of estrogen and progesterone on tone and spontaneous rhythmic contractions of the rabbit bladder. Urol Res 27: 386–392, 1999.[CrossRef][ISI][Medline]
  33. Shimonovitz S, Monga AK, and Stanton SL. Does the menstrual cycle influence cystometry? Int Urogynecol J Pelvic Floor Dysfunct 8: 213–215, 1997.[Medline]
  34. imuni V, Banovi I, Ciglar S, Jeren L, Pavici Baldini D, and prem M. Local estrogen treatment in patients with urogenital symptoms. Int J Gynaecol Obstet 82: 187–197, 2003.[Medline]
  35. Takeda H, Yamazaki Y, Igawa Y, Kaidoh K, Akahane S, Miyata H, Nishizawa O, Akahane M, and Andersson KE. Effects of {beta}3-adrenoceptor stimulation on prostaglandin E2-induced bladder hyperactivity and on the cardiovascular system in conscious rats. Neurourol Urodyn 21: 558–565, 2002.[CrossRef][Medline]
  36. Temple JL, Bradshaw HB, Wood E, and Berkley KJ. Effects of hypogastric neurectomy on escape responses to uterine distention in the rat. Pain Suppl 6: S13–S20, 1999.
  37. Visco AG, Cholhan HJ, O'Toole L, and Guzick DS. Effects of menstrual cycle and urinary tract instrumentation on uroflowmetry. Neurourol Urodyn 19: 147–152, 2000.[CrossRef][ISI][Medline]
  38. Woods M, Carson N, Norton NW, Sheldon JH, and Argentieri TM. Efficacy of the {beta}3-adrenergic receptor agonist CL-316243 on experimental bladder hyperreflexia and detrusor instability in the rat. J Urol 166: 1142–1147, 2001.[CrossRef][Medline]
  39. Yamazaki Y, Takeda H, Akahane M, Igawa Y, Nishizawa O, and Ajisawa Y. Species differences in the distribution of {beta}-adrenoceptor subtypes in bladder smooth muscle. Br J Pharmacol 124: 593–599, 1998.[CrossRef]
  40. Yono M, Yoshida M, Takahashi W, Inadome A, Seshita H, Miyamoto Y, and Ueda S. Effects of ovarian hormones on {beta}-adrenergic receptor-mediated relaxation in the female rabbit bladder. Urol Res 28: 38–45, 2000.[CrossRef][Medline]




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