Effects of raloxifene on the urethra of adult castrated female rats.

OBJECTIVE: The objective of this study was to evaluate the effects of raloxifene on the weight and epithelial thickness of the urethra of castrated female rats. METHODS: Forty castrated female rats were randomly separated into two groups: group I (control, n = 20) received only the vehicle, and group II (raloxifene, n = 20) received 750 microg/day of raloxifene for 30 days. On the 31st day, the animals were sacrificed and the urethras were removed for the study. A model for categorical data using the weighted minimum mean square error method and Student's t test were used for the data analysis (p < 0.05). RESULTS: The mean weights of the urethras in groups I and II were 22 +/- 1.6 mg and 24 +/- 1.7 mg, respectively (p = 0.371). There was an increase in the mean epithelial thickness of the distal segments in group II compared to group I (50.7 +/- 1.9 microm vs. 45.3 +/- 1.6 microm, respectively) (p < 0.04). No statistically significant difference was found in the mean epithelial thickness of the proximal urethra between the two groups (p = 0.187). CONCLUSION: Raloxifene administered to castrated female rats for 30 days increased the distal urethral epithelial thickness and did not alter the weight of the urethra.

Krametosan, a new trinorlignan from the roots of Krameria tomentosa.

A new phenylcoumarone type trinorlignan, krametosan (1), along with the known norlignans, ratanhiaphenol I (2) and 2-(2'-hydroxy-4',6'-dimethoxyphenyl)-5-(E)-propenylbenzofuran (3), the lignan conocarpan (4) and dinorlignan decurrenal (5), were isolated from the CHCl3 extract of the roots of Krameria tomentosa. The structure of these compounds were elucidated by the spectroscopic methods.

Detection system for ocular refractive error measurement.

An automatic and objective system for measuring ocular refractive errors (myopia, hyperopia and astigmatism) was developed. The system consists of projecting a light target (a ring), using a diode laser (lambda = 850 nm), at the fundus of the patient's eye. The light beams scattered from the retina are submitted to an optical system and are analysed with regard to their vergence by a CCD detector (matrix). This system uses the same basic principle for the projection of beams into the tested eye as some commercial refractors, but it is innovative regarding the ring-shaped measuring target for the projection system and the detection system where a matrix detector provides a wider range of measurement and a less complex system for the optical alignment. Also a dedicated electronic circuit was not necessary for treating the electronic signals from the detector (as the usual refractors do); instead a commercial frame grabber was used and software based on the heuristic search technique was developed. All the guiding equations that describe the system as well as the image processing procedure are presented in detail. Measurements in model eyes and in human eyes are in good agreement with retinoscopic measurements and they are also as precise as these kinds of measurements require (0.125D and 5 degrees).

Sex-related differences in the analgesic response to the rat tail immersion test.

The analgesic response was evaluated by the tail immersion test in adult male (N = 30), female (N = 21) and androgenized female Wistar rats (N = 15). The reaction time for tail withdrawal from the hot water bath was faster for male than for female rats (3.48 +/- 0.12 vs 6.46 +/- 0.42 s). The reaction time of androgenized female rats was similar to that of male rats (3.08 +/- 0.16 s). Blockade of opiate receptors with naloxone (2 mg/kg, ip) decreased the sensitivity to the noxious stimuli in males (4.08 +/- 0.10 s) and in androgenized females (3.69 +/- 0.19 s) but increased it in female rats (5.01 +/- 0.41 s). These data show sex-related differences in the analgesic response evaluated by the tail immersion test and indicate that administration of androgens to newborn female rats affects their pain sensitivity.

Sex-related differences in the analgesic response to the rat tail immersion test

The analgesic response was evaluated by the tail immersion test in adult male (N = 30), female (N = 21) and androgenized female Wistar rats (N = 15). The reaction time for tail withdrawal from the hot water bath was faster for male than for female rats (3.48 +/- 0.12 vs 6.46 +/- 0.42 s). The reaction time of androgenized female rats was similar to that of male rats (3.08 +/- 0.16 s). Blockade of opiate receptors with naloxone (2 mg/kg, ip) decreased the sensitivity to the noxious stimuli in males (4.08 +/- 0.10 s) and in androgenized females (3.69 +/- 0.19 s) but increased it in female rats (5.01 +/- 0.41 s). These data show sex-related differences in the analgesic response evaluated by the tail immersion test and indicate that administration of androgens to newborn female rats affects their pain sensitivity.

The effects of forebrain multiple lesions on the pressor response induced by bilateral carotid occlusion in conscious rats.

In the present study, the effects of electrolytic lesions of the anteroventral third ventricle (AV3V) region and of the medial forebrain bundle (MFB) on the pressor response induced by bilateral carotid occlusion (BCO) in conscious intact and aortic baroreceptor-denervated (AD) rats were investigated. In intact control rats, BCO during 60 s produced a pressor response that could be divided into an early response (ER = 50 +/- 3 mmHg) that reachs a peak during the first 20 s and a sustained late response (LR), smaller than ER (32 +/- 2 mmHg), observed during the last 30 s. In intact-innervated rats, AV3V lesion (2 days) reduced ER (22 +/- 3 mmHg) and LR (16 +/- 2 mmHg), whereas the bilateral MFB lesions (6 days) mainly reduced LR (9 +/- 1 mmHg). Rats with simultaneous lesion of both the AV3V region and the MFB showed additional reduction of the ER (15 +/- 3 mmHg), but not LR (11 +/- 1 mmHg) when compared to the effect of MFB lesions alone. Compared to the AV3V lesion alone, LR but not ER was reduced in rats with a double lesion. In sham-lesioned rats, AD induced a significant increase in the pressor response to BCO (ER = 75 +/- 4 mmHg and LR = 65 +/- 3 mmHg) when compared to intact controls.(ABSTRACT TRUNCATED AT 250 WORDS)

Sex-related differences in cardiovascular responses to common carotid occlusion in conscious rats.

Mean arterial pressure and heart rate were determined in conscious, unrestrained groups of 10 male, female and androgenized female Wistar rats 20 s (early pressor response) and 1 min (late sustained response) after bilateral carotid artery occlusion. The early pressor response, which is of carotid reflex origin, was 40% greater in female than in male rats (45 +/- 2 vs 63 +/- 3 mmHg, respectively). The late sustained response, which is of central origin (probably ischemic), did not differ between male and female rats (32 +/- 2 vs 37 +/- 4 mmHg, respectively). The magnitude of the early pressor response of androgenized female rats (50 +/- 2 mmHg) was similar to that of male rats (45 +/- 2 mmHg) but the late sustained response was 19% smaller (26 +/- 2 mmHg). Common carotid occlusion caused increases in heart rate which were greater in female (51 +/- 9 and 34 +/- 9 beats/min in the early pressor response and late sustained response, respectively) than in male rats (31 +/- 5 and 8 +/- 4 beats/min, respectively). In androgenized female rats, heart rate decreased during common carotid occlusion (34 +/- 7 and 35 +/- 8 beats/min after 20s and 1 min, respectively). These data provide evidence that there are substantial sex-related differences in the cardiovascular responses to common carotid occlusion in conscious rats and indicate that administration of androgens to newborn female rats affects the baroreceptor reflex control of their arterial pressure.

Sex-related differences in cardiovascular responses to common carotid occlusion in conscious rats

Mean arterial pressure and heart rate were determined in conscious, unrestrained groups of 10 male, female and androgenized female Wistar rats 20 s (early pressor response) and 1 min (late sustained response) after bilateral carotid artery occlusion. The early pressor response, which is carotid reflex origin, was 40% greater in female than in male rats (45 ñ 2 vs 63 ñ 3 mmHg, respectively). The late sustained response, which is of central origin (probably ischemic), did not differ between male and female rats (32 ñ 2 vs 37 ñ 4 mmHg, respectively). The magnitude of the early pressor response of androgenized female rats (50 ñ 2 mmHg) was similar to that of male rats (45 ñ 2 mmHg) but the late sustained response was 19% smaller (26 ñ 2 mmHg). Common carotid occlusion caused increases in haert rate which were greater in female (51 ñ 9 and 34 ñ 9 beats/min in the early pressor response and late sustained response respectively) than in male rats (31 ñ 5 and 8 ñ 4 beats/min, respectively). In androgenized female rats, heart rate decreased during common carotid occlusion (34 ñ 7 and 35 ñ 8 beats/min after 20 s and 1 min, respectively). These data provide evidence that there are substantial sex-related differences in the cardiovascular responses to common carotid occlusion in conscoious rats and indicate that administration of androgens to newborn female rats affects the baroreceptor reflex control of their arterial pressure

Effect of testosterone on the pressor response to common carotid occlusion in gonadectomized conscious male rats with lesion of the median eminence.

The influence of testosterone on the development of the pressor response to common carotid occlusion was investigated in control and median eminence-lesioned male rats. In control rats (N = 9), gonadectomy performed 21 days before the experiments reduced by 22% (from 51 +/- 2 to 40 +/- 2 mmHg) and treatment with testosterone (300 micrograms for 4 days before the measurements) increased the initial peak pressor response (from 51 +/- 2 to 57 +/- 2 mmHg) which depends on carotid innervation. The maintained response which is of central origin (probably ischemic) was less affected. In nongonadectomized rats (N = 6), lesions of median eminence (6 days) decreased the initial peak by 19% (from 52 +/- 2 to 42 +/- 3 mmHg) and the maintained response by 56% (from 32 +/- 2 to 14 +/- 1 mmHg). Sham-operated rats served as controls. In gonadectomized animals (N = 6) the lesion reduced only the maintained response (from 23 +/- 2 to 11 +/- 1 mmHg). Testosterone supplementation restored the maintained response but did not alter the initial peak. These results indicate that the pressor response to common carotid occlusion in male rats is modulated by testosterone and that the depression in the maintained response caused by median eminence lesion can be reversed by steroid supplementation.

Participation of opioid receptors in the modulation of the analgesic response by adrenal and gonadal glands.

The involvement of opioid receptors in the analgesic response was evaluated by the tail-immersion test in simultaneously adrenalectomized and ovariectomized female Wistar rats (210-250 g). The reaction time (mean +/- SEM) for tail withdrawal from hot water decreased significantly 2 weeks after surgery (3.52 +/- 0.20 s) when compared to intact animals (6.09 +/- 0.23 s). Hormonal replacement with dexamethasone (50 micrograms/day) did not affect reaction time (3.38 +/- 0.19 s). However, this response was restored by combined adrenal and gonadal steroid substitution (estradiol 5 micrograms/day and progesterone 1.5 micrograms 6 h before the tests) therapy (5.11 +/- 0.45 s in animals treated with dexamethasone plus estradiol and 5.04 +/- 0.43 s in animals treated with dexamethasone plus estradiol plus progesterone). Naloxone (2 mg/kg) decreased the reaction time of animals treated with adrenal and gonadal steroids (5.11 +/- 0.45 vs 4.15 +/- 0.44 s and 5.04 +/- 0.43 vs 3.87 +/- 0.28 s, respectively, before and after naloxone) but failed to decrease it in rats treated with dexamethasone only (3.88 +/- 0.18 vs 4.34 +/- 0.25 s, before and after naloxone). These observations indicate that gonadal steroids are the most important steroid factors involved in the reaction time to tail immersion in hot water and confirm other reports that the opioid pathways modulating the neuronal circuitry require the presence of these hormones.

The effect of tubero-infundibular dopaminergic neurons on prolactin and alpha-melanocyte stimulating hormone release.

The effect of tubero-infundibular dopaminergic neurons (TIDA) on the release of prolactin (PRL) and alpha-melanocyte stimulating hormone (alpha-MSH) was studied in median eminence-lesioned (MEL) male rats (N = 6-28). Plasma PRL and alpha-MSH levels were significantly elevated 2 (86.1 +/- 19.8 and 505.1 +/- 19.1 ng/ml), 4 (278.7 +/- 15.5 and 487.4 +/- 125.1 ng/ml), 7 (116.2 +/- 16.2 and 495.8 +/- 62.6 ng/ml) and 14 (247.3 +/- 26.1 and 448.4 +/- 63.8 ng/ml) days after MEL when compared to sham-operated control animals (55.5 +/- 13.4 and 56.2 +/- 6.1 ng/ml, respectively). MEL altered plasma PRL and alpha-MSH levels in a differential manner, with a 1.5- to 5.0-fold increase in PRL and an 8.0- to 9.0-fold increase in alpha-MSH. The increase of alpha-MSH levels occurred abruptly and remained constant from days 2 to 14. These observations indicate that TIDA plays an important role in the pituitary release of PRL and alpha-MSH and provide evidence that the release of the two hormones occurs in a differential manner.

The effect of tubero-infundibular dopaminergic neurons on prolactin and alpha-melanocyte stimulating hormone release

The effect of tubero-infundibular dopaminergic neurons (TIDA) on the release of prolactin (PRL) and alpha-melanocyte stimulating hormone (alpha-MSH) was studied in median eminence-lesioned (MEL) male rats (N = 6-28). Plasma PRL and alpha-MSH levels were significantly elevated 2(86.1 ñ 19.8 and 505.1 ñ 19.1 ng/ml), 4(278.7 ñ 15.5 and 487.4 ñ 125.1 ng/ml), 7 (116.2 ñ 16.2 and 495.8 ñ 62.6 ng/ml) and 14 (247.3 ñ 26.1 and 448.4 ñ 63.8 ng/ml) days after MEL when compared to sham-operated control animals (55.5 ñ 13.4 and 56.2 ñ 6.1 ng/ml, repectively). MEL altered plasma PRL and alpha-MSH levels in a diffential manner, with 1.5-to5.0-fold increase in PRL and an 8.0- to 9.0-fold increase in alpha-MSH. The increase of alpha-MSH levels occured abruptly and remained constant from days 2 to 14. These observations indicate that TIDA plays an important role in the pituitary release of PRL and alpha-MSH and provide evidence that the release of the two hormones occurs in a differential manner

Participation of opioid receptors in the modulation of the analgesic response by adrenal and gonadal glands

The invovlement of opiodi receptors in the analgesic response was evaluated by the tail-immersion test in simultaneously adrenalectomized and ovariectomized female Wistar rats (210-250g). The reaction time (mean ñ SEM) for tail withdrawal from hot water decreased significantly 2 weeks after surgery (3.52 ñ 0.20 s) when compared to intact animals (6.09 ñ 0.23 s). Hormonal replacement with dexamethasone (50*/day) did not affect reaction time (3.38 ñ 0.19 s). However, this response was restored by combined adrenal and gonadal steroid substitution (estradiol 5*g/day and progesterone 1.5*g 6h before the test) therapy (5.11 ñ 0.45 s) in animal treated with dexamethasone plus estradiol and 5.04 ñ 0.43 s in animals treated with dexamethasone plus estradiol plus progesterone). Naloxone (2mg/Kg decreased the reaction time of animals treated with adrenal and gonadal steroids (5.11 ñ 0.45 vs 4.15 ñ 0.44 and 5.04 ñ 0.43 vs 3.87 ñ 0.28 s, respectively, before and after naloxone) but failed to decrease it in rats treated with dexamethasone only (3.88 ñ 0.18 vs 4.34 ñ 0.25 s, before and after naloxone). These observations indicate that gonadal steroids are the most important steroid factors involved in the reaction time to tail immersion in hot water and confirm other reports that the opioid pathways modulating the neuronal circuitry require the presence of these hormones

Involvement of beta-adrenergic receptors in the differential release of gonadotropins in acutely orchidectomized rats.

To determine the differential release of gonadotropins in acutely orchidectomized rats, a single injection of the beta-adrenergic blocker Bornaprolol (FM 24) was administered to the animals and plasma FSH and LH levels were determined. FM 24 produced low plasma FSH levels only when injected 16 h before starting the blood collection and had no effect on FSH levels at 0, 30 and 46 h after its administration. However, it produced low LH plasma levels at 0, 16 and 30 h after administration. These findings confirm that pituitary beta-adrenergic receptors are involved in plasma LH release and suggest that they could also be involved in the differential release of FSH/LH.

The effect of age on the pressor response produced by common carotid artery occlusion in conscious rats.

The pressor responses to 60 s of common carotid artery occlusion were studied in conscious male rats of different ages. Compared to rats at the age of 2 months, the initial peak and the maintained response in 6- 12- and 18-month old rats were well preserved. In 1-month old rats, both components were significantly depressed but in 24-month old rats only the initial peak of the pressor response was markedly attenuated. These findings demonstrate that age is an important factor in the response to common carotid artery occlusion which is more marked for the initial peak than the maintained response.

The role of opioids in the analgesic response of rats during the estrous cycle.

The analgesic response was evaluated by the tail immersion test in female rats during each phase of the estrous cycle. The reaction time (mean +/- SEM) for tail withdrawal from the hot water bath was faster during proestrus (5.78 +/- 0.28 s) and decreased significantly during estrus (5.31 +/- 0.30 s) and diestrus 1 (5.40 +/- 0.21 s). Blockade of opiate receptors with naloxone (2 mg/kg, ip) increased the sensitivity to the noxious stimulus only during proestrus (6.46 +/- 0.42 vs 5.02 +/- 0.41 s). These results suggest that the effects of gonadal steroids on nociception may involve an opioid pathway.

Pressor responses to common carotid occlusion in female rats: effects of gonadectomy and treatment with gonadal steroid hormones.

The pressor responses to common carotid occlusion were studied in conscious female rats throughout the estrous cycle, after gonadectomy and after gonadectomy followed by treatment with estrogen and progesterone. The initial peak pressor response was highest during proestrus and fell significantly over the remaining 3 days of the estrous cycle. The maintained pressor response was relatively unchanged throughout the cycle, except during diestrus 1 when it decreased markedly. Gonadectomy reduced and treatment with estradiol alone increased the initial pressor component, respectively. Treatment of gonadectomized rats with estradiol plus progesterone enhanced both components. These findings suggest that gonadal steroid hormones are important modulators of the pressor response to common carotid occlusion.