Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 12 de 12
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Clinics (Sao Paulo) ; 76: e2926, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34495079

RESUMO

OBJECTIVES: To describe the MORPHEOS (Morbidity in patients with uncontrolled HTN and OSA) trial, and describe the challenges imposed by the COVID-19 pandemic. METHODS: MORPHEOS is a multicenter (n=6) randomized controlled trial designed to evaluate the blood pressure (BP) lowering effects of treatment with continuous positive airway pressure (CPAP) or placebo (nasal strips) for 6 months in adult patients with uncontrolled hypertension (HTN) and moderate-to-severe obstructive sleep apnea (OSA). Patients using at least one antihypertensive medication were included. Uncontrolled HTN was confirmed by at least one abnormal parameter in the 24-hour ABPM and ≥80% medication adherence evaluated by pill counting after the run-in period. OSA was defined by an apnea-hypopnea index ≥15 events/hours. The co-primary endpoints are brachial BP (office and ambulatory BP monitoring, ABPM) and central BP. Secondary outcomes include hypertension-mediated organ damage (HMOD) to heart, aorta, eye, and kidney. We pre-specified several sub-studies from this investigation. Visits occur once a week in the first month and once a month thereafter. The programmed sample size was 176 patients but the pandemic prevented this final target. A post-hoc power analysis will be calculated from the final sample. ClinicalTrials.gov: NCT02270658. RESULTS: The first 100 patients are predominantly males (n=69), age: 52±10 years, body mass index: 32.7±3.9 kg/m2 with frequent co-morbidities. CONCLUSIONS: The MORPHEOS trial has a unique study design including a run-in period; pill counting, and detailed analysis of hypertension-mediated organ damage in patients with uncontrolled HTN that will allow clarification of the impact of OSA treatment with CPAP.


Assuntos
COVID-19 , Hipertensão , Apneia Obstrutiva do Sono , Adulto , Pressão Sanguínea , Pressão Positiva Contínua nas Vias Aéreas , Humanos , Hipertensão/epidemiologia , Hipertensão/terapia , Masculino , Pessoa de Meia-Idade , Pandemias , SARS-CoV-2 , Apneia Obstrutiva do Sono/terapia
2.
Clinics ; Clinics;76: e2926, 2021. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1339699

RESUMO

OBJECTIVES: To describe the MORPHEOS (Morbidity in patients with uncontrolled HTN and OSA) trial, and describe the challenges imposed by the COVID-19 pandemic. METHODS: MORPHEOS is a multicenter (n=6) randomized controlled trial designed to evaluate the blood pressure (BP) lowering effects of treatment with continuous positive airway pressure (CPAP) or placebo (nasal strips) for 6 months in adult patients with uncontrolled hypertension (HTN) and moderate-to-severe obstructive sleep apnea (OSA). Patients using at least one antihypertensive medication were included. Uncontrolled HTN was confirmed by at least one abnormal parameter in the 24-hour ABPM and ≥80% medication adherence evaluated by pill counting after the run-in period. OSA was defined by an apnea-hypopnea index ≥15 events/hours. The co-primary endpoints are brachial BP (office and ambulatory BP monitoring, ABPM) and central BP. Secondary outcomes include hypertension-mediated organ damage (HMOD) to heart, aorta, eye, and kidney. We pre-specified several sub-studies from this investigation. Visits occur once a week in the first month and once a month thereafter. The programmed sample size was 176 patients but the pandemic prevented this final target. A post-hoc power analysis will be calculated from the final sample. ClinicalTrials.gov: NCT02270658. RESULTS: The first 100 patients are predominantly males (n=69), age: 52±10 years, body mass index: 32.7±3.9 kg/m2 with frequent co-morbidities. CONCLUSIONS: The MORPHEOS trial has a unique study design including a run-in period; pill counting, and detailed analysis of hypertension-mediated organ damage in patients with uncontrolled HTN that will allow clarification of the impact of OSA treatment with CPAP.


Assuntos
Humanos , Masculino , Adulto , Pessoa de Meia-Idade , Apneia Obstrutiva do Sono/terapia , COVID-19 , Hipertensão/terapia , Hipertensão/epidemiologia , Pressão Sanguínea , Pressão Positiva Contínua nas Vias Aéreas , Pandemias , SARS-CoV-2
3.
Mol Cell Endocrinol ; 404: 141-50, 2015 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-25657045

RESUMO

Herein, we characterized the spatio-temporal expression, cellular distribution and regulation by androgens of the ß-defensin SPAG11C, the rat ortholog of the human SPAG11B isoform C, in the developing epididymis by using RT-PCR, in situ hybridization and immunohistochemistry. We observed that Spag11c mRNA was ubiquitously expressed in rat fetuses, but preferentially detected in male reproductive tissues at adulthood. SPAG11C (mRNA and protein) was prenatally mainly detected in the mesenchyme of the Wolffian duct, switching gradually after birth to a predominant localization in the epididymis epithelium during postnatal development. In the adult epididymis, smooth muscle and interstitial cells were also identified as sources of SPAG11C. Furthermore, SPAG11C was differentially immunolocalized on spermatozoa surface during their transit from testis throughout caput and cauda epididymis. Developmental and surgical castration studies suggested that androgens contribute to the epididymal cell type- and region-specific modulation of SPAG11C mRNA levels and immunolocalization. Together our findings provide novel insights into the potential role of ß-defensins in the epididymis.


Assuntos
Androgênios/farmacologia , Embrião de Mamíferos/anatomia & histologia , Epididimo/crescimento & desenvolvimento , Ductos Mesonéfricos/metabolismo , beta-Defensinas/genética , beta-Defensinas/metabolismo , Animais , Embrião de Mamíferos/metabolismo , Epididimo/metabolismo , Imuno-Histoquímica , Hibridização In Situ , Células Intersticiais do Testículo/metabolismo , Masculino , Músculo Liso/metabolismo , Orquiectomia , Especificidade de Órgãos , Ratos , Ratos Wistar , Reação em Cadeia da Polimerase em Tempo Real
4.
J Androl ; 32(6): 614-24, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21764896

RESUMO

Inflammation is a primordial host response to invasion by pathogens or tissue injury. During infection, microbes can activate immune cells through pattern-recognition receptors, such as Toll-like receptors, an evolutionarily conserved family of receptors that mediate innate immunity in a wide range of organisms. Infection also triggers an increase in glucocorticoid levels as part of the stress response. The scenario indicates that these signals have to be well integrated to mount an effective host response to infection and injury. The mechanisms by which innate and adaptive immunity are regulated, as well as the intersection of these responses with glucocorticoids and the glucocorticoid receptor (GR) in the epididymis, an organ essential for the transport, maturation, storage, and protection of the spermatozoa, are not well understood. In this review we bring together recent data demonstrating the cellular and biochemical machinery involved in the response of the adult rat epididymis to a bacterial product challenge. We also illustrate the basic aspects of the expression, localization, function, and regulation of the GR by steroid hormones (androgens and glucocorticoids) within the epididymis. We conclude with considerations of controversial or still unanswered topics about GR, now emerging as a regulatory step in epididymal biology, its functional relationship with androgens and androgen receptor, and the innate immune response of the epididymis. How these topics may be of interest as part of future research in the area, and how they ultimately can help us to better understand the epididymal function under noninflammatory and inflammatory conditions, are also discussed.


Assuntos
Epididimo/imunologia , Glucocorticoides/imunologia , Glucocorticoides/metabolismo , Imunidade Inata , Animais , Infecções Bacterianas/imunologia , Epididimite/imunologia , Epididimite/microbiologia , Humanos , Masculino , Camundongos , Ratos , Receptores de Glucocorticoides/metabolismo , Receptores Toll-Like/imunologia , Receptores Toll-Like/metabolismo
5.
Mol Cell Endocrinol ; 325(1-2): 64-77, 2010 Aug 30.
Artigo em Inglês | MEDLINE | ID: mdl-20573576

RESUMO

Glucocorticoids regulate several physiological functions, including reproduction, in mammals. Curiously, little is known about glucocorticoid-induced effects on the epididymis, an androgen-dependent tissue with vital role on sperm maturation. Here, RT-PCR, Western blot and immunohistochemical studies were performed to evaluate expression, cellular distribution and hormonal regulation of glucocorticoid receptor (GR) along rat epididymis. The rat orthologue of human GRalpha (mRNA and protein) was detected in caput, corpus and cauda epididymis and immunolocalized in the nucleus and cytoplasm of different epididymal cells (epithelial, smooth muscle and interstitial cells) and nerve fibers. Changes in plasma glucocorticoid and androgen levels differentially regulated GR expression in caput and cauda epididymis by homologous and heterologous mechanisms. In vivo treatment with dexamethasone significantly changed the expression of glucocorticoid-responsive genes and induced ligand-dependent GR nuclear translocation in epithelial cells from epididymis, indicating that GR is fully active in this tissue. Heterologous regulation of androgen receptor expression by glucocorticoids was also demonstrated in cauda epididymis. Our results demonstrate that the epididymis is under glucocorticoid regulation, opening new insights into the roles of this hormone in male fertility.


Assuntos
Epididimo/efeitos dos fármacos , Epididimo/metabolismo , Hormônios Esteroides Gonadais/farmacologia , Receptores de Glucocorticoides/genética , Receptores de Glucocorticoides/metabolismo , Adrenalectomia , Fatores Etários , Androgênios/sangue , Animais , Fertilidade/genética , Regulação da Expressão Gênica/efeitos dos fármacos , Glucocorticoides/farmacologia , Hormônios Esteroides Gonadais/sangue , Masculino , Orquiectomia , Ratos , Ratos Wistar , Receptores de Glucocorticoides/fisiologia , Distribuição Tecidual/efeitos dos fármacos
6.
Biol Reprod ; 79(6): 1135-47, 2008 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18703421

RESUMO

This study provides the first evidence that rat epididymis is fully capable of initiating an inflammatory response to lipopolysaccharide (LPS) from Escherichia coli through activation of Toll-like receptor 4 (TLR4). TLR4 functionality was demonstrated by in vivo LPS challenge, which induced a time- and dose-dependent activation of the transcription factor nuclear factor kappa B (NFKB) in caput and cauda epididymides. NFKB activation by LPS in caput epididymidis was abrogated when rats were pretreated with the NFKB inhibitor PDTC, confirming the specificity of this response. Within 2 h of LPS treatment (0.01 and 1 mg/kg, i.v.), NFKB activation in caput and cauda was accompanied by upregulation of Il1b, Nfkbia, and Cd14, but not Tlr4, mRNA. These effects, however, were not sustained after 24 h of LPS treatment. Lipopolysaccharide systemic effects were not restricted to epididymides, since Il1b, Nfkbia, and Cd14 mRNAs were also upregulated in other male reproductive tissues from LPS-treated rats (1 mg/kg, i.v., 2 h). Constitutive TLR4 was immunolocalized in some, but not all, epididymal epithelial cells and in interstitial cells, some of them identified as resident ED2-positive macrophages. No change in TLR4 immunostaining pattern was observed when epididymides from control and LPS-treated rats were compared (1 mg/kg, i.v., 2 h and 24 h). Significant NFKB activation was also achieved within 1 min of in vitro incubation of caput epididymidis with LPS (0.01-5 mug/ml), confirming that components for TLR4 signaling cascade activation are fully active in this tissue. This study contributes to a better understanding of the innate immune response in the epididymis and other tissues from the male reproductive tract.


Assuntos
Epididimo/efeitos dos fármacos , Epididimo/metabolismo , Escherichia coli/química , Lipopolissacarídeos/farmacologia , Receptor 4 Toll-Like/metabolismo , Animais , Western Blotting , Corticosterona/sangue , Ensaio de Desvio de Mobilidade Eletroforética , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/metabolismo , Imuno-Histoquímica , Técnicas In Vitro , Interleucina-1beta/biossíntese , Interleucina-1beta/genética , Receptores de Lipopolissacarídeos/biossíntese , Receptores de Lipopolissacarídeos/genética , Masculino , NF-kappa B/biossíntese , NF-kappa B/genética , Ratos , Ratos Wistar , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transdução de Sinais/efeitos dos fármacos , Testosterona/sangue
7.
Mol Hum Reprod ; 14(2): 85-96, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18204069

RESUMO

This study reports the genomic organization of the rhesus alpha(1A)-adrenoceptor gene (ADRA1A). Full-length cloning of rhesus ADRA1A splice variants was achieved by combining PCR screening of a seminal vesicle cDNA library and 5'-RACE assays with total RNA from seminal vesicle. The classical ADRA1A mRNA (ADRA1A_v1) and six full-length ADRA1A splice variants were identified representing transcripts that code for functional (ADRA1A_v1, ADRA1A_v2a, ADRA1A_v3a, ADRA1A_v3d, ADRA1A_v3e) and truncated (ADRA1A_v2c and ADRA1A_v3c) receptor isoforms. Comparative analysis of the deduced amino acid sequence indicated that rhesus ADRA1A_i1 isoform (corresponding to the ADRA1A_v1 transcript) shares high identity to the amino acid sequence present in the classical alpha(1A)-adrenoceptor from human and other mammalian species. Partial nucleotide sequences for rhesus alpha(1B)-(ADRA1B) and alpha(1D)-adrenoceptor (ADRA1D) transcripts were also characterized. RT-PCR studies indicated differential distribution of all ADRA1A-related splice variants as well as ADRA1B and ADRA1D mRNAs, in tissues from rhesus and human male reproductive tract. Immunohistochemistry revealed alpha(1A)-adrenoceptor (ADRA1A_i1) immunostaining in smooth muscle cells and epithelial cells of rhesus efferent ductules, epididymis and seminal vesicle. Taken together the present results demonstrate that the complexity of the splicing mechanisms involved in the regulation of the ADRA1A gene is not restricted to human and is a common characteristic among Old World monkeys.


Assuntos
Perfilação da Expressão Gênica , Receptores Adrenérgicos alfa 1/genética , Receptores Adrenérgicos alfa 1/metabolismo , Processamento Alternativo , Sequência de Aminoácidos , Animais , Clonagem Molecular , Epididimo/metabolismo , Humanos , Imuno-Histoquímica , Macaca mulatta , Masculino , Dados de Sequência Molecular , Próstata/metabolismo , RNA Mensageiro/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Glândulas Seminais/metabolismo , Testículo/metabolismo
8.
Reprod Biol Endocrinol ; 5: 29, 2007 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-17623071

RESUMO

BACKGROUND: Relaxin is the endogenous ligand of the G-protein coupled receptor RXFP1, previously known as LGR7. In humans relaxin can also activate, but with lower affinity, the closely related receptor for the insulin-like peptide from Leydig cells, RXFP2, previously known as LGR8. The lack of relaxin impairs male fertility but the precise distribution and the function of relaxin receptors in the male reproductive tract is not known. We investigated the distribution of Rxfp1 and Rxfp2 in the reproductive tract of the male rat and the function of relaxin in the vas deferens, a tissue with high expression of both receptors. METHODS: The presence of mRNA for Rxfp1 and Rxfp2 was investigated in testes, cultured Sertoli cells, epididymis, vas deferens, seminal vesicle, prostate, and spermatozoa by RT-PCR and Southern blot. Protein expression in the testis, vas deferens, primary culture of Sertoli cells, and spermatozoa was assessed by immunohistochemistry and immunofluorescence. The role of relaxin in the vas deferens was evaluated by contractility studies and radioimmunoassay of cAMP production. The effect of relaxin on mRNA levels for metalloproteinase-7 was measured by Northern blot. RESULTS: Transcripts for Rxfp1 and Rxfp2 were present in almost all parts of the male reproductive tract, with high levels in testis and vas deferens. Both receptors were immunolocalized in late stage germ cells but not in mature spermatozoa, although mRNAs for both receptors were also present in mature spermatozoa. Rxfp1 but not Rxfp2 was detected in cultured Sertoli cells. Strong immunostaining for Rxfp1 and Rxfp2 was seen in muscular and epithelial layers of the vas deferens and in arteriolar walls. Relaxin did not affect contractility and cyclic AMP production of the vas deferens, but increased the levels of mRNA for metalloproteinase-7. CONCLUSION: Rxfp1 and Rxfp2 are widely and similarly distributed throughout the male reproductive tract. Our results suggest that Rxfp1 on spermatids and Sertoli cells may be important in spermatogenesis. Relaxin in the vas deferens does not affect contractility, but may affect vascular compliance and collagen and matrix remodeling.


Assuntos
Mapeamento Cromossômico , Família Multigênica , RNA Mensageiro/metabolismo , Receptores Acoplados a Proteínas G/genética , Receptores de Peptídeos/genética , Relaxina/metabolismo , Testículo/química , Ducto Deferente/química , Animais , Feminino , Masculino , Ratos , Ratos Wistar , Receptores Acoplados a Proteínas G/metabolismo , Receptores de Peptídeos/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Suínos , Testículo/citologia , Testículo/metabolismo , Ducto Deferente/citologia , Ducto Deferente/metabolismo
9.
Cell Tissue Res ; 325(1): 125-33, 2006 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-16541288

RESUMO

Microtubule-associated protein 1B (MAP 1B) is a neuronal cytoskeleton marker with predominant expression in the developing nervous system. The present study provides evidence for the expression of this cytoskeleton protein in non-neuronal and neuronal cells along rat and human efferent ductules and epididymis (initial segment, caput, and cauda). Reverse transcription/polymerase chain reaction and Western blot analysis were used to confirm the presence of MAP 1B (mRNA and protein) in rat tissues. Immunohistochemical studies revealed MAP-1B-positive staining in columnar ciliated cells present in efferent ductules and in narrow cells located in the initial segment, in both rat and human. MAP-1B-positive basal cells, located underneath the columnar cells, were only identified in the initial segment and caput epididymidis of the rat. Qualitative analysis of tissues from 40-day-old and 120-day-old rats indicated that the number of MAP-1B-positive ciliated, narrow, and basal cells per tubule increased with sexual maturation. These immunoreactive cells did not stain for dopamine beta-hydroxylase or acetylcholinesterase, indicating that they were not adrenergic or cholinergic in nature. Immunohistochemical studies also revealed the presence of MAP-1B-positive staining in interstitial nerve fibers in caput and cauda epididymidis from both rat and human. Thus, the expression of MAP 1B is not confined to a specific cell type in rat and human efferent ductules and epididymis. The functional significance of this cytoskeleton protein in tissues from the male reproductive tract requires further investigation.


Assuntos
Epididimo/citologia , Epididimo/metabolismo , Proteínas Associadas aos Microtúbulos/análise , Rede do Testículo/citologia , Rede do Testículo/metabolismo , Animais , Humanos , Imuno-Histoquímica , Masculino , Ratos , Ratos Wistar
10.
Life Sci ; 75(12): 1449-63, 2004 Aug 06.
Artigo em Inglês | MEDLINE | ID: mdl-15240180

RESUMO

This study analyses possible changes during surgical and chemical castration in the expression and pharmacological characteristics of alpha1-adrenoceptor in adult rat seminal vesicle. Ribonuclease protection assays indicated that alpha1a--was the predominant mRNA, while alpha1b-and alpha1d-adrenoceptor transcripts were detected in lower abundance in this tissue. alpha1a-adrenoceptor mRNA expression presented a complex dependency on androgens, while alpha1b- and alpha1d-adrenoceptor transcripts were both upregulated with surgical and chemical castration, suggesting a negative modulation by androgens. Testosterone treatment reversed the effects caused by surgical castration. Functional studies confirmed the involvement of alpha1A- and alpha1B-adrenoceptor in the seminal vesicle contractile responses, and suggested that alpha1B-induced contractile response was upregulated after castration. Taken together, the results suggest that alpha1-adrenoceptor expression in seminal vesicle is differentially regulated by the androgen status of the rat.


Assuntos
Androgênios/farmacologia , Clonidina/análogos & derivados , Regulação da Expressão Gênica/efeitos dos fármacos , RNA Mensageiro/metabolismo , Receptores Adrenérgicos alfa 1/metabolismo , Glândulas Seminais/metabolismo , Antagonistas de Receptores Adrenérgicos alfa 1 , Análise de Variância , Animais , Autorradiografia , Compostos de Bário , Cloretos/fisiologia , Acetato de Ciproterona/antagonistas & inibidores , Dioxanos , Masculino , Orquiectomia , Tamanho do Órgão , Fenilefrina , Piperazinas , Quinazolinas , Quinoxalinas , Ratos , Ratos Wistar , Glândulas Seminais/fisiologia , Testosterona/sangue , Testosterona/farmacologia
11.
J Androl ; 23(3): 374-83, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12002439

RESUMO

In the present work, histochemical and biochemical studies were conducted to analyze changes in the pattern of autonomic innervation during sexual maturation, using the rat epididymis as a model. Glyoxylic acid histochemistry and immunohistochemical studies against dopamine beta-hydroxylase (DbetaH) and acetylcholinesterase (AChE) indicated a reduction in the amount of catecholaminergic and AChE-positive neurons, fibers, and puncta detected in the cauda epididymis of adult rats (120 days old), when compared to immature (40 days) and young adult (60 days) animals. No obvious age-related variations were detected in the few catecholaminergic and AChE-positive fibers and puncta present in the caput region. AChE-positive fibers were found sorting out among epithelial cells and ending free upon the epithelial surface or into the tubular lumen of the cauda region of adult rats. Furthermore, a positive staining for AChE in epithelial cells was also detected in the caput and cauda epididymis in all ages studied. Biochemical analysis confirmed a significant decrease in noradrenaline concentration as well as AChE activity in the cauda epididymis with sexual maturation. Immunohistochemical studies against microtubule-associated protein 1B (MAP 1B), a neuronal cytoskeletal marker, further substantiated the quantitative changes observed in catecholaminergic and AChE-positive neuronal elements in the cauda epididymis. Thus, our results documented segment-specific variations in noradrenaline concentration and AChE activity during epididymal sexual maturation and suggest that such variations result, at least in part, from the refinement of the autonomic innervation pattern with age.


Assuntos
Acetilcolinesterase/metabolismo , Sistema Nervoso Autônomo/enzimologia , Catecolaminas/metabolismo , Epididimo/crescimento & desenvolvimento , Epididimo/inervação , Fatores Etários , Animais , Sistema Nervoso Autônomo/química , Sistema Nervoso Autônomo/crescimento & desenvolvimento , Dopamina beta-Hidroxilase/análise , Epididimo/anatomia & histologia , Fertilidade , Glioxilatos/análise , Imuno-Histoquímica , Masculino , Proteínas Associadas aos Microtúbulos/análise , Tamanho do Órgão , Ratos , Ratos Wistar , Maturidade Sexual
12.
Biol Reprod ; 66(2): 508-15, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11804969

RESUMO

We have characterized the expression of alpha1-adrenoceptor in epididymis from rats in different stages of sexual maturation: 40 (immature), 60 (young adult), and 120 (adult) days of age. Plasma testosterone levels were low in the immature animals but increased significantly in the 60- and 120-day-old animals. These changes were followed by a progressive increase in rat body weight and in caput and cauda epididymis relative weight. Reverse transcription polymerase chain reaction assay indicated that alpha1a-, alpha1b-, and alpha1d-adrenoceptor transcripts were present in both caput and cauda epididymis from adult rats. Ribonuclease protection assays further indicated that the expression of these alpha1-adrenoceptor transcripts differed with age and epididymal region analyzed. Prazosin (nonselective alpha1 antagonist), 5-methyl urapidil (alpha1A-selective), and BMY 7378 (alpha1D-selective) displaced [3H]prazosin binding curves in caput and cauda epididymis from 40- and 120-day-old rats. The potency order for these antagonists, as calculated from the negative logarithm of the inhibition constant (pK(i)) values for the high-affinity sites, indicated a predominant population of alpha1A-adrenoceptor subtype in caput and cauda epididymis from adult animals. Differences in pK(i) values in caput and cauda epididymis from immature and adult animals also suggested that the relative amount of alpha1-adrenoceptors, at the protein level, is modulated by sexual maturation. Taken together, the changes in alpha1-adrenoceptor expression during sexual maturation may suggest specific roles for these receptors in epididymal function.


Assuntos
Epididimo/metabolismo , Receptores Adrenérgicos alfa 1/metabolismo , Maturidade Sexual/fisiologia , Antagonistas Adrenérgicos alfa/metabolismo , Animais , Ligação Competitiva , Epididimo/efeitos dos fármacos , Hibridização In Situ , Masculino , Membranas/efeitos dos fármacos , Membranas/metabolismo , Ensaios de Proteção de Nucleases , Tamanho do Órgão/efeitos dos fármacos , Tamanho do Órgão/fisiologia , Prazosina/metabolismo , RNA Mensageiro/biossíntese , RNA Mensageiro/isolamento & purificação , Ensaio Radioligante , Ratos , Ratos Wistar , Receptores Adrenérgicos alfa 1/biossíntese , Receptores Adrenérgicos alfa 1/efeitos dos fármacos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Testosterona/sangue
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA