ABSTRACT
At present, there is no reliable in vitro assembled prepubertal testis-like biomimetic organ culture system designed to assess the functional effects of human gonadotropins on Sertoli and Leydig cells. Spermatogenesis is regulated by endocrine, paracrine, and juxtacrine factors (testicular cross-talk), mainly orchestrated by gonadotropins such as luteinizing hormone (LH) and follicle-stimulating hormone (FSH) that play a pivotal role by stimulating Leydig and Sertoli cells, respectively. The aim of our study was to set up an in vitro prepubertal porcine bioengineered construct as a new model for experimental studies on reassembled Sertoli and Leydig cells. We have evaluated Sertoli and Leydig cells obtained from 15- to 20-day-old neonatal pig testes in terms of purity and function. Subsequently, purified Sertoli and enriched Leydig cells were subjected to coincubation to obtain an in vitro prepubertal porcine testis-like culture system. We performed enzyme-linked immunosorbent assay (ELISA) for anti-Müllerian hormone (AMH), inhibin B, and testosterone secretion in the medium, and Real-Time PCR analysis of AMH, inhibin B, FSH-r, aromatase, LHr, and 3β-HSD mRNA expression levels. This in vitro testis-like system was highly responsive to the effects of human gonadotropins and testosterone. AMH mRNA expression and secretion declined, and inhibin-B increased, while FSH-receptor expression was downregulated upon FSH/LH exposure/treatment. Finally, the production of testosterone was increased selectively upon LH treatment. In summary, our proposed model could help to better determine the action of human gonadotropins on Sertoli and Leydig cells. The potential usefulness of the system for shedding light into male infertility-related issues is evident.
Subject(s)
Animals , Male , 3-Hydroxysteroid Dehydrogenases/metabolism , Animals, Newborn , Anti-Mullerian Hormone/metabolism , Aromatase/metabolism , Cell Culture Techniques , Enzyme-Linked Immunosorbent Assay , Follicle Stimulating Hormone/pharmacology , Hormones/pharmacology , In Vitro Techniques , Inhibins/metabolism , Leydig Cells/metabolism , Luteinizing Hormone/pharmacology , Models, Biological , Real-Time Polymerase Chain Reaction , Receptors, FSH/metabolism , Receptors, LH/metabolism , Sertoli Cells/metabolism , Swine , Testis/metabolism , Testosterone/metabolismABSTRACT
The aim of the study was to provide a descriptive analysis of familial male-limited precocious puberty (FMPP), which is a rare inherited disease caused by heterozygous constitutively activating mutations of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR). The patient was a ten-month-old boy, presenting with penile enlargement, pubic hair formation, and spontaneous erections. Based on the clinical manifestations and laboratory data, including sexual characteristics, serum testosterone levels, GnRH stimulation test, and bone age, this boy was diagnosed with peripheral precocious puberty. Subsequently the precocious puberty-related genes were analyzed by direct DNA sequencing of amplified PCR products from the patient and his parents. Genetic analysis revealed a novel heterozygous missense mutation c.1732G>C (Asp578His) of the LHCGR gene exon11 in the patient, which had never been reported. His parents had no mutations. After combined treatment with aromatase inhibitor letrozole and anti-androgen spironolactone for six months, the patient's symptoms were controlled. The findings in this study expand the mutation spectrum of the LHCGR gene, and provide molecular evidence for the etiologic diagnosis as well as for the genetic counseling and prenatal diagnosis in the family.
Subject(s)
Humans , Infant , Male , Heterozygote , Mutation , Puberty, Precocious , Drug Therapy , Genetics , Receptors, LH , Chemistry , GeneticsABSTRACT
<p><b>OBJECTIVE</b>To investigate the effects of Morina Officinalis How (MOH) on the abnormal levels of serum luteotrophic hormone (LH) and LH receptor (LHR) in the testis tissue induced by cellphone radiation (CPR) in rats.</p><p><b>METHODS</b>Fifty adult male SD rats were randomly divided into five groups of equal number: sham CPR, untreated CPR, negative double distilled water (DDW) control, aqueous MOH extract, and alcohol MOH extract. All the animals were exposed to mobile phone radiation except those of the sham CPR group. Then, the rats of the latter two groups were treated intragastrically with MOH at 20 g per kg of the body weight per day in water and alcohol, respectively. After 2. weeks of treatment, all the rats were sacrificed for measurement of the levels of serum LH and LHR in the testis tissue.</p><p><b>RESULTS</b>The levels of serum LH and LHR were 30.15 ± 8.71 and 33.28 ± 6.61 in the aqueous MOH group and 0.96 ± 0.06 and 0.94 ± 0.08 in the alcohol MOH group, both significantly decreased as compared with the negative DDW controls (P < 0.05), but with no remarkable difference between the two MOH groups (P > 0.05).</p><p><b>CONCLUSION</b>MOH can improve CPR-induced abnormality of LH and LHR in adult male rats.</p>
Subject(s)
Animals , Male , Rats , Cell Phone , Electromagnetic Radiation , Luteinizing Hormone , Blood , Radiation Effects , Morinda , Chemistry , Radiation Injuries, Experimental , Blood , Drug Therapy , Random Allocation , Receptors, LH , Blood , Radiation Effects , Testis , Radiation EffectsABSTRACT
The effect of high concentrations of testosterone on ovarian follicle development was investigated. Primary follicles and granulosa cells were cultured in vitro in media supplemented with a testosterone concentration gradient. The combined effects of testosterone and follicle-stimulating hormone (FSH) on follicular growth and granulosa cell gonadotropin receptor mRNA expression were also investigated. Follicle growth in the presence of high testosterone concentrations was promoted at early stages (days 1-7), but inhibited at later stage (days 7-14) of in vitro culture. Interestingly, testosterone-induced follicle development arrest was rescued by treatment with high concentrations of FSH (400 mIU/mL). In addition, in cultured granulosa cells, high testosterone concentrations induced cell proliferation, and increased the mRNA expression level of FSH receptor (FSHR), and luteinized hormone/choriogonadotropin receptor. It was concluded that high concentrations of testosterone inhibited follicle development, most likely through regulation of the FSH signaling pathway, although independently from FSHR downregulation. These findings are an important step in further understanding the pathogenesis of polycystic ovary syndrome.
Subject(s)
Animals , Female , Mice , Androgens , Pharmacology , Cell Proliferation , Follicle Stimulating Hormone , Genetics , Metabolism , Pharmacology , Gene Expression Regulation, Developmental , Granulosa Cells , Cell Biology , Metabolism , Ovarian Follicle , Cell Biology , Metabolism , Primary Cell Culture , RNA, Messenger , Genetics , Metabolism , Receptors, FSH , Genetics , Metabolism , Receptors, Gonadotropin , Genetics , Metabolism , Receptors, LH , Genetics , Metabolism , Signal Transduction , Genetics , Testosterone , PharmacologyABSTRACT
<p><b>OBJECTIVE</b>To assess the association of rs13405728 polymorphism of luteinizing hormone receptor (LHR) gene with slow ovarian response during assisted reproductive technology (ART).</p><p><b>METHODS</b>Two hundred and thirty-six women were enrolled and grouped according to their genotypes. The rs13405728 polymorphism was genotyped by DNA sequencing.</p><p><b>RESULTS</b>No signifiicant difference was found in antral follicle count and anti-Mullerian hormone between the three genotypes (P>0.05). The incidence of slow response in genotype GG was lower than in the other two genotypes (P<0.05). There was no significant difference in the amount of follicle stimulating hormone required, the number of follicles ≥14 mm on human chorionic gonadotrophin day, oocytes, mature oocytes, available embryos, and the clinical pregnancy rate among the three genotypes (P>0.05). There was an independent correlation between slow ovarian response with the genotypes of rs13405728, the initial dose of gonadotropin, and the dose of luteinizing hormone required (P<0.05).</p><p><b>CONCLUSION</b>Rs13405728 of the LHR gene may be associated with slow ovarian response in ART. Various mechanisms may be involved in the poor response and slow response.</p>
Subject(s)
Adult , Female , Humans , Fertilization in Vitro , Methods , Gene Frequency , Genotype , Logistic Models , Ovarian Reserve , Genetics , Ovulation Induction , Methods , Polymorphism, Single Nucleotide , Receptors, LH , Genetics , Reproductive Techniques, Assisted , Sequence Analysis, DNA , MethodsABSTRACT
The aim of this study was to investigate the effects of different Luteinizing hormone (LH) and steroid hormones levels on LH receptor (LHR) expression in the hippocampal cells. Rats (24 males and 24 females) were assigned to four groups: one control and three experimental [gonadectomy (GDX), gonadectomy + gonadotropin releasing hormone analogue (GDX+GnRHa) and GDX+GnRHa+estradiol (E2) or testosterone (T)] independently for each gender. All experimental rats were gonadectomized; then GnRHa was administrated to GDX+GnRHa group, and GnRHa plus steroid hormone to GDX+GnRHa+E2 or T group in both genders for four-month. LHR mRNA expression and its protein level in hippocampal cells were measured using QRT-PCR and Western blotting. Quantification of mRNA revealed a decrease in LHR transcripts level in GDX+GnRHa group of females. A significant change was observed between GDX groups and GDX+GnRHa+E2 or T versus GDX+GnRHa group in females. High levels of LH decreased significantly the immature isoform of LHR in GDX group compared to control group in both genders, but low LH concentrations in GDX+GnRHa group induced immature LHR isoform production only in females. Therefore increased LH concentration induces production of incomplete LHR transcripts in hippocampal cells and decreases immature LHR at the protein level. This implies that LH decreases the efficiency of translation through either producing non-functional LHR molecules or preventing their translation.
Subject(s)
Animals , DNA Primers/genetics , Estradiol/biosynthesis , Female , Gene Expression Regulation , Gonadotropin-Releasing Hormone/metabolism , Hippocampus/cytology , Hippocampus/metabolism , Hormones/metabolism , Luteinizing Hormone/biosynthesis , Male , Neurons/metabolism , Protein Isoforms , RNA, Messenger/metabolism , Rats , Rats, Wistar , Receptors, LH/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction/methods , Steroids/metabolism , Testosterone/biosynthesisABSTRACT
<p><b>OBJECTIVE</b>Familial male-limited precocious puberty (FMPP) is due to constitutive activation of a mutant luteinizing hormone/choriogonadotropin receptor (LH/CGR) leading to elevated testosterone synthesis in testicular Leydig cells. In the present study, we have analyzed the LHCGR gene for members of a Chinese FMPP family.</p><p><b>METHODS</b>Physical examinations have included assessment of penile length, testicular volume and pubic hair. Bone age assessment, levels of testosterone and gonadotropin-releasing hormone (GnRH) stimulations tests were measured. DNA was extracted from blood samples of the proband and his parents using an QIAGEN Blood DNA Mini Kit. The 11 exons of LHCGR gene were amplified using an AmpliTaq PCR system, and the PCR products were sequenced using an ABI3130xl Genetic Analyzer.</p><p><b>RESULTS</b>The affected boy was 3 year and 1 month old and showed typical clinical manifestation of peripheral precocious puberty. His height was 116.8cm (+5.1s) and Tanner stages were PH 2. Testicular volume was 8 mL bilaterally, penile was 8.5 cm × 2.5 cm. Basal testosterone was 2310 ng/L and bone age was 9 years. GnRH stimulation test revealed a prepubertal response to gonadotropin. The peak of LH was 2.66 IU/L, and the peak of FSH was 1.03 IU/L. Upon sequencing exon 11 of the LHCGR, a heterozygous point mutation of nucleotide 1703 from C to T was detected, which resulted in an amino acid transition from Ala (GCC) to Val (GTC) at position 568. Thus the mutation of LHCGR gene was confirmed to be constitutively active. After treating with aromatase inhibitors for half a year, the patient showed an increase in bone age and height by half a year and 4 cm, respectively. The same point mutation was detected in the patient's father, but did not have any influence on his puberty development.</p><p><b>CONCLUSION</b>A novel point mutation of the LHCGR gene has been identified in a family affected with FMPP. The c.1703C>T mutant LHCGR was confirmed to be constitutively active, which has led to maturation and proliferation of Leydig cells. The variable phenotype within the family suggested variable expressivity of the disease.</p>
Subject(s)
Adult , Child, Preschool , Humans , Male , Amino Acid Substitution , Base Sequence , Codon , Exons , Models, Molecular , Mutation , Protein Conformation , Puberty, Precocious , Diagnosis , Genetics , Receptors, LH , Chemistry , GeneticsABSTRACT
Endometritis is one of the primary reasons for reproductive failure. In order to investigate endometritis-associated marker proteins, proteomic analysis was performed on bovine endometrium with endometritis. In bovine endometritis, desmin, alpha-actin-2, heat-shock protein (HSP) 27, peroxiredoxin-6, luteinizing hormone receptor isoform 1, collectin-43 precursor, deoxyribonuclease-I (DNase-I), and MHC class I heavy chain (MHC-Ih) were up-regulated. In contrast, transferrin, interleukin-2 precursor, hemoglobin beta subunit, and potassium channel tetramerisation domain-containing 11 (KCTD11) were down-regulated in comparison to normal endometrium. The proteomic results were validated by semiquantitative-PCR and immunoblot analysis. The mRNA levels of desmin, transferrin, alpha-actin-2, HSP27, KCTD11, and MHC-Ih were up-regulated by over 1.5-fold, and showed a pattern similar to their proteomic profiles. Desmin and alpha-actin-2 protein showed positive correlations between proteomic analysis and immunoblot analysis. These results suggest that desmin and alpha-actin-2 may play important roles in endometritis-related function, and could be useful markers for the diagnosis of bovine endometritis.
Subject(s)
Female , Actins , Collectins , Desmin , Endometritis , Endometrium , Heat-Shock Proteins , Hemoglobins , Interleukin-2 , Potassium Channels , Proteins , Proteomics , Receptors, LH , RNA, Messenger , TransferrinABSTRACT
OBJECTIVE: To analyze the aberrant expression of the GIPR and LHCGR in different forms of adrenocortical hyperplasia: ACTH-independent macronodular adrenal hyperplasia (AIMAH), primary pigmented nodular adrenocortical disease (PPNAD) and diffuse adrenal hyperplasia secondary to Cushing's disease (DAHCD). METHODS: We quantified GIPR and LHCGR expressions using real time PCR in 20 patients with adrenocortical hyperplasia (seven with AIMAH, five with PPNAD, and eight with DAHCD). Normal adrenals tissues were used as control and the relative expression was compared with β-actin. RESULTS: GIPR and LHCGR expressions were demonstrated in all tissues studied. Median GIPR and LHCGR mRNA levels were 1.6; 0.4; 0.5 and 1.3; 0.9; 1.0 in adrenocortical tissues from AIMAH, PPNAD and DAHCD respectively. There were no differences between GIPR and LHCGR expressions in all tissues studied. CONCLUSIONS: GIPR and LHCGR overexpression were not identified in the studied cases, thus suggesting that this molecular mechanism is not involved in adrenocortical hyperplasia in our patients.
OBJETIVO: Analisar a expressão aberrante do GIPR e do LHCGR em diferentes formas de hiperplasias adrenocorticais: hiperplasia adrenal macronodular independente de ACTH (AIMAH), doença adrenocortical nodular pigmentada primária (PPNAD) e hiperplasia adrenal difusa secundária à doença de Cushing (DAHCD). MÉTODOS: Quantificou-se por PCR em tempo real a expressão desses receptores em 20 pacientes: sete com AIMAH, cinco com PPNAD e oito com DAHCD. Adrenais normais foram utilizadas como controle e a expressão relativa desses receptores foi comparada à expressão da β-actina. RESULTADOS: A expressão desses receptores foi demonstrada em todos os tecidos estudados. A mediana da expressão do GIPR e do LHCGR foi de 1,6; 0,4; 0,5 e de 1,3; 0,9; 1,0 nos tecidos dos pacientes com AIMAH, PPNAD e DAHCD, respectivamente. Não houve diferença significativa na expressão desses receptores nos tecidos estudados. CONCLUSÕES: Hiperexpressão do GIPR e do LHCGR não foi observada, sugerindo que esse mecanismo não está envolvido na patogênese molecular da hiperplasia adrenal nesses pacientes.
Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Adrenal Cortex Diseases/metabolism , Adrenal Glands/pathology , Pituitary ACTH Hypersecretion/metabolism , Receptors, Gastrointestinal Hormone/metabolism , Receptors, LH/metabolism , Actins/metabolism , Adrenal Cortex Diseases/genetics , Adrenal Glands/metabolism , Hyperplasia/metabolism , Polymerase Chain Reaction , Pituitary ACTH Hypersecretion/genetics , Reverse Transcriptase Polymerase Chain Reaction , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Gastrointestinal Hormone/genetics , Receptors, LH/genetics , Young AdultABSTRACT
The purpose of the present research was to investigate the effects of polymorphisms of luteinizing hormone receptor (LHR) and follicle-stimulating hormone receptor (FSHR) genes, evaluated by polymerase chain reaction-restriction fragment length polymorphism in European-Zebu composite beef heifers from six different breed compositions. The polymorphism site analysis from digestion with HhaI and AluI restriction endonucleases allowed the genotype identification for LHR (TT, CT and CC) and FSHR (GG, CG and CC) genes. A high frequency of heterozygous animals was recorded in all breed compositions for both genes, except in two compositions for LHR. The probability of pregnancy (PP) at first breeding was used to evaluate the polymorphism effect on sexual precocity. The PP was analyzed as a binary trait, with a value of 1 (success) assigned to heifers that were diagnosed pregnant by rectal palpation and a value of 0 (failure) assigned to those that were not pregnant at that time. Heterozygous heifers showed a higher pregnancy rate (67 and 66% for LHR and FSHR genes, respectively), but no significant effects were observed for the genes studied (P = 0.9188 and 0.8831 for LHR and FSHR, respectively) on the PP. These results do not justify the inclusion of LHR and FSHR restriction fragment length polymorphism markers in selection programs for sexual precocity in beef heifers. Nevertheless, these markers make possible the genotype characterization and may be used in additional studies to evaluate the genetic structure in other bovine populations.
Subject(s)
Animals , Male , Female , Cattle/genetics , Crosses, Genetic , Polymorphism, Genetic , Receptors, FSH/genetics , Receptors, LH/genetics , Genotype , Meat , Polymerase Chain Reaction , Reproduction/geneticsABSTRACT
As modificações nas concentrações das gonadotrofinas ao longo da vida reprodutiva dependem de amadurecimento funcional harmônico entre conexões neurais, neurônios-GnRH no hipotálamo, gonadotropos hipofisários e células da granulosa e teca da parede folicular. As concentrações de LH e FSH sofrem variações com o período do dia, fase do ciclo menstrual e idades ginecológica e cronológica. A variação circadiana é marcante para o LH e ocorre na fase puberal, quando os pulsos têm maior freqüência e amplitude no período noturno. Na fase puberal tardia, os pulsos das gonadotrofinas ocorrem também durante o dia e perdem a variação noite-dia, permanecendo discretas alterações durante as 24 horas do dia. No ciclo menstrual, durante os anos reprodutivos, o FSH eleva-se no final da fase lútea tardia, declina na fase folicular média, eleva-se bruscamente na fase ovulatória e permanece em níveis basais até a fase lútea tardia. O LH permanece em níveis constantes durante toda a fase folicular, eleva-se no pico ovulatório e declina a níveis basais na fase lútea. Na quarta década, há modificações hipotálamo-neurais na secreção de GnRH, atenuação do retrocontrole positivo exercido pelo estradiol e diminuição na freqüência e prolongamento dos pulsos de GnRH. A hipófise responde com diminuição na densidade de receptores-GnRH, perda da sensibilidade do gonadotropo, secreção de gonadotrofinas mais básicas com maior meia-vida, diminuição na freqüência e maior amplitude dos pulsos de LH e FSH e secreção preferencial de FSH. Estas modificações, associadas à aceleração no consumo folicular, explicam a elevação monotrópica mais rápida de FSH após os 37-38 anos e a manutenção de níveis quase constantes de LH até o final do período reprodutivo. Estudos consistentes mostram que a elevação seletiva dos níveis basais de FSH na fase folicular precoce na verdade é gradual, sendo observada já na terceira década de vida. A discordância entre pulsos e níveis basais de FSH...
Changes in the levels of gonadotropins throughout the reproductive life depend on a fine tuned functional development of neural pathways and GnRH-neurones, pituitary gonadotrophs and granulosa-theca cells of the follicular wall. Both, LH and FSH levels change according to the day-time, menstrual cycle phase, and gynecological age. Initiating the puberty, changes in LH pulses are remarkable, showing higher frequency and amplitude at night. Later in puberty, the pulses of LH are also maintained during the day, remaining its levels with very little variation within the 24 hours period. During the menstrual cycle, the FSH levels increase at the end of the luteal phase, decrease during the medium and late follicular phase, increase rapidly in the ovulatory phase and remain at low basal levels until the late luteal phase. The levels of LH remain unaltered during the whole follicular phase, increase in the ovulatory surge, and decrease to the basal levels in the luteal phase. At the forth decade of life, the GnRH secretion changes, with hypothalamic loss of sensitivy to the estradiol positive feedback and decrease in frequency and prolongation of the GnRH pulses. The pituitary response is atenuated due to decrease in the density of GnRH receptors on gonadotroph cells, loss of gonadotroph sensitivity, secretion of more basic FSH and LH molecules, decrease in frequency and increase in amplitude of LH and FSH pulses. These modifications result in monotropic increase of the FSH secretion. Current studies show that the selective increase in the FSH levels in the early follicular phase is gradual, beginning as early as the third decade of life. These alterations in FSH are associated with an accelerated follicular depletion in women after 37-38 years old. On the other side, the LH levels remain almost constant up to the end of reproductive life. The different levels of FSH and LH seen throughout the reproductive years may be due to yet unknown regulatory...
Subject(s)
Humans , Female , Follicle Stimulating Hormone, Human , Gonadotropin-Releasing Hormone , Luteinizing Hormone , Receptors, FSH , Receptors, LHABSTRACT
O objetivo deste estudo foi quantificar por PCR em tempo real a expressão dos genes dos receptores do peptídeo insulinotrópico dependente de glicose (GIPR) e do hormônio luteinizante (LHCGR) em tumores e hiperplasias adrenocorticais (hiperplasia adrenal macronodular independente de ACTH; doença nodular adrenocortical pigmentosa primária e aumento da adrenal associado à neoplasia endócrina múltipla tipo 1). O nível de expressão do GIPR foi mais elevado nos tumores malignos que nos benignos em pacientes adultos e pediátricos, enquanto o nível de expressão do LHCGR foi extremamente baixo nos tumores malignos em pacientes adultos. Não se observou diferença no nível de expressão de ambos os receptores nas diferentes formas de hiperplasia.
The aim of this study was to quantify by real-time PCR the gene expression of glucose-dependent insulinotropic peptide receptor (GIPR) and luteinizing hormone receptor (LHCGR) in adrenocortical tumors and hyperplasia (ACTH-independent macronodular adrenal hyperplasia, primary pigmented nodular adrenocortical disease and adrenal enlargement associated with multiple endocrine neoplasia type 1. The GIPR expression level was more elevated in the malignant tumors that in the benign ones, of both adult and pediatric patients, whereas the level of LHCGR expression was extremely low in malignant tumors of adult patients. No difference in the expression level of these receptors was observed in the different forms of adrenocortical hyperplasia.
Subject(s)
Humans , Male , Female , Adrenocortical Hyperfunction , Multiple Endocrine Neoplasia , Gastric Inhibitory Polypeptide , Gene Expression , Immunohistochemistry , Loss of Heterozygosity , Mutation/genetics , Polymerase Chain Reaction , Receptors, LH , Receptors, PeptideABSTRACT
PURPOSE: Ethane 1,2-Dimethane sulfonate (EDS), an alkylating agent, has been widely used to create the testosterone withdrawal rat model. The present study was carried out to test the effect of EDS administration on the expression of steroidogenesis-related genes in the rat testis and on epididymal sperm counts. MATERIALS AND METHODS: Adult male Sprague-Dawley rats (300~350 g B.W.) were injected with a single dose of EDS (75 mg/kg, i.p.) and sacrificed on days 0, 7, 14, 21, 28, 35, 42, and 49. Tissue weights (testis, epididymis and seminal vesicle) were measured, and serum LH levels were determined by specific radioimmunoassay. The transcriptional activities of LH receptor (LH-R), 3beta-hydroxysteroid dehydrogenase (3beta-HSD), and steroidogenic acute regulatory protein (StAR) were evaluated by semi-quantitative RT-PCR. RESULTS: Weights of the reproductive and accessory organs declined progressively after the EDS treatment (weeks 1~3). After this, the decrease stopped, with a gradual return towards normal. Full recovery was observed in testis and seminal vesicle evaluations on weeks 5 and 6, respectively. Only 70% recovery was found in epididymis during weeks 5~7. A more dramatic drop was observed in caput epididymal sperm count, and the maximum recovery was 40% on week 7. Serum LH level increased significantly on week 2 after EDS treatment, then gradually decreased during weeks 3~5. The transcripts for the steroidogenesis-related genes in testis declined sharply during weeks 1~2, then returned to normal on week 4. CONCLUSIONS: Our results demonstrate that EDS might directly induce severe damage, such as tissue destruction and decreased sperm counts, in epididymis compared to those in testis and seminal vesicles. Changes in the activities of testicular steroidogenesis-related genes caused by abrupt death and repopulation of Leydig cells in EDS-treated rats were in good correlation with other parameters shown in this and previouslypublished data. Taken together, the EDS injection model might be useful to understand not only the mechanism of differentiation of testicular somatic and germ cells but also the function of the epididymis in the aging process.
Subject(s)
Adult , Animals , Humans , Male , Rats , Aging , Epididymis , Ethane , Germ Cells , Leydig Cells , Models, Animal , Oxidoreductases , Radioimmunoassay , Rats, Sprague-Dawley , Receptors, LH , Seminal Vesicles , Sperm Count , Spermatozoa , Testis , Testosterone , Weights and MeasuresABSTRACT
A population of 370 European-Zebu composite beef heifers, consisting of six different breed compositions (A-F), were characterized genetically, using RFLP markers of luteinizing hormone receptor (LHR) and follicle-stimulating hormone receptor (FSHR) genes. Our objectives were to genetically characterize this population and to determine the structure and the genetic variability of this hybrid herd. The genotypes were determined through PCR, followed by digestion with restriction endonucleases. The PCR-RFLP analysis made it possible to identify the LHR and FSHR genotypes, as well as to characterize the degree of heterozygosis, which was high for all of the breed compositions, for both loci, except for two combinations for LHR (B and C). The observed heterozygosity (Ho) was lower than the expected heterozygosity (He) for compositions C (for LHR) and A and D (for FSHR); however, for the population as a whole, Ho was above He (with a mean of 57 versus 46%, respectively), reflecting the elevated genetic variability in this population and also the informative value of the RFLP markers, which could be useful for population genetic characterization studies. The analysis of the degree of genetic structure of this population, estimated by the Nei's statistic, for both loci, indicated an elevated total genetic diversity (HT = 47%), with most of this variability being due to intrapopulational diversity (HS = 46%), with a low degree of genetic differentiation among the six breed compositions (GST = 1.2%). The estimates generated by the Wright's F statistic indicated a non-endogamic population, with excess heterozygotes (FIT = -0.22), which was also observed at the intrapopulational level (FIS = -0.23). The results gave evidence that the genetic selection applied to this European-Zebu composite population did not affect the expected high genetic variability for this type of crossbreeding, which makes it possible to use these animals to obtain economically valuable productiv...
Subject(s)
Animals , Female , Genetic Variation , Cattle/genetics , Receptors, FSH/genetics , Receptors, LH/genetics , Alleles , Genetic Carrier Screening , Genotype , Genetic Markers/genetics , Polymorphism, Restriction Fragment Length , Polymerase Chain ReactionABSTRACT
OBJECTIVE: We performed immunohistochemistry for the evaluation of follicle stimulating hormone receptor (FSHR), luteinizing hormone receptor (LHR) expression in the ovarian tumors and examined the blood level of the gonadotropins in ovarian cancer patients to investigate ovarian carcinogenesis process related to gonadotropins. METHODS: Between January 2002 and July 2003, 25 patients with ovarian tumors were treated in the Hallym University Sacred Heart Hospital. 25 ovarian tumors including 7 borderline tumors, 1 sex cord stromal tumor, 1 germ cell tumor, and 16 carcinomas were examined for FSHR, LHR expression by immunohistochemistry. Serum gonadotropins were collected from 13 cases of 25 ovarian tumors who were not taking hormones at the time of blood collection. RESULTS: Followings are results summarized. 1. Mean FSH levels were lower among cases compared with controls. LH levels were lower among cases than controls, but the difference was not statistically significant. 2. The steady decline of FSHR, LHR expression from borderline tumor (86%, 100%) to carcinoma (56%, 43%) is observed. 3. Patients showing significant gonadotropins receptors expression showed lower serum FSH and LH levels when compared with patients with no detectable gonadotropins receptors. CONCLUSION: The presence of FSHR, LHR in ovarian tumors provide additional evidence supporting the relation of gonadotropins and ovarian carcinogenesis. But, this study did not support the hypothesis that pituitary goandotropins increase the risk of ovarian cancer. The decline of receptor expression from borderline tumors to carcinoma suggests that FSH, LH may be needed in early ovarian cancer development. If further studies of gonadal peptides and gonadotropins are done, we can suggest the cut-off value of gonadotropins on ovarian carcinogenesis.
Subject(s)
Humans , Carcinogenesis , Gonadotropins , Gonads , Heart , Immunohistochemistry , Neoplasms, Germ Cell and Embryonal , Ovarian Neoplasms , Peptides , Receptors, FSH , Receptors, Gonadotropin , Receptors, LH , Sex Cord-Gonadal Stromal TumorsABSTRACT
OBJECTIVES: To investigate the effect of LH receptor in folliculogenesis, we confirm the expression level of LH receptor (LH-R) mRNA in human granulosa cells (GCs) and its expression levels were analyzed by comparison to embryo developmental rate and pregnancy rate. MATERIALS AND METHODS: GCs were obtained at the time of oocyte retrieval from the patients undergoing IVF-ET program. The patients were divided into two groups: Group I (n=20) is poor responder (retrieved oocyte(s)3ea). After the extraction of total RNA, semiquantitative RT-PCR was performed and the expression level of LH-R mRNA was normalized by beta-actin. Statistical analysis was performed by using Chi(2) test, Student's t-test and Pearson correlation. RESULTS: In Group II, the relative values of LH-R mRNA (0.680 vs. 0.463, p<0.005) and pregnancy rate (54.7% vs. 23.1%, p<0.05) were significantly higher than in Group I. Number of retrieved oocyte(s) was gradually increased when the expression of LH-R mRNA was increased (p<0.05). But the quality of retrieved oocyte and transferred embryo were not related with the expression of LH-R mRNA. When the pregnancy rate was compared with FSH only group and FSH combined with hMG group in the ovarian stimulation protocol, FSH combined with hMG group was significantly higher than FSH only group in Group I (37.5% vs. 0%), and the expression of LH-R mRNA was significantly higher in hMG combined group than FSH only group (p<0.05). CONCLUSION: Expression level of LH-R mRNA has important role in ovarian function related with the response to gonadotrophin in human folliculogenesis. Furthermore these data might provide the evidence that additional use of hMG is helpful to poor responders.
Subject(s)
Female , Humans , Pregnancy , Actins , Embryonic Development , Embryonic Structures , Granulosa Cells , Oocyte Retrieval , Oocytes , Ovulation Induction , Pregnancy Rate , Receptors, LH , RNA , RNA, MessengerABSTRACT
The clinical models for studying ovary-determining genes may be premature ovarian failure (POF). POF is a condition causing amenorrhea, hypoestrogenism, and elevated gonadotropins in women under 40 years old. FSH receptor, LH receptor, inhibin, GDF-9 (growth differentiation factor-9), BMP-15 (bone morphogenetic protein-15), DIAPH2 (diaphanous gene) and XPNPEP2 (X-prolyl aminopeptidase) genes were proposed as a possible candidate gene, but until recently, only mutations in FSH receptor, LH receptor and inhibin genes have been identified in POF patients. Therefore mutation screening of another POF gene necessary to reveal the principal causative genes of POF. OBJECTIVE: The present study was performed to analyze the mutation of GDF-9 gene in Korean patient with POF and to investigate whether mutation of these gene is a likely main cause of POF. METHODS: Eighty-six women with POF were studied and thirty-six normal women were enrolled as control. Mutation screening of these genes were performed by denaturing HPLC and were confirmed by automatic sequencing. RESULTS: Three different mutations of GDF-9 gene were identified in Korean women with POF; Arg3Cys mutation in one patient, Leu40Val mutation in one patient, Asp57Tyr mutation in 10 patients and 5 normal controls. Arg3Cys mutation and Leu40Val mutation were likely cause of disease. Frequencies of Arg3Cys mutation and Leu40Val mutation were 1.2%, respectively. Asp57Tyr mutation was common polymorphism in Korean women. All mutations was a novel mutation found in the present study. CONCLUSION: POF was resulted by mutations of GDF-9 gene, but mutations of GDF-9 gene are not likely main causes of POF because of low frequency of mutations.
Subject(s)
Adult , Female , Humans , Amenorrhea , Bone Morphogenetic Protein 15 , Chromatography, High Pressure Liquid , Gonadotropins , Growth Differentiation Factor 9 , Inhibins , Mass Screening , Primary Ovarian Insufficiency , Receptors, FSH , Receptors, LHSubject(s)
Humans , Male , Female , Spermatids , Oligospermia/etiology , Blood/analysis , Vagina/diagnostic imaging , Vagina , Receptors, LHABSTRACT
As açöes fundamentais das gonadotrofinas hipofisárias na vida sexual reprodutiva de ambos os sexos dependem da integridade estrutural e funcional dos seus respectivos receptores, Os receptores das gonadotrofinas localizados na membrana citoplasmàtica säo membros da grande família dos receptores acoplados à proteína G e apresentam uma estrutura comum caracterizada por uma extensa porçäo extracelular e setes hélices transmembranas. A recente identificaçäo de mutaçöes inativadoras e ativadoras de ocorrência natural nos genes dos receptores do LH e do FSH contribuíram para a maior compreensäo de estados patológicos gonadais. Neste trabalho, revisamos os aspectos moleculares dos defeitos dos genes dos receptores das gonadotrofinas e suas implicaçöes fenotípicas no sexo feminino. Nas mulheres com mutaçöes inativadoras em homozigose nestes genes, sintomas freqüentes como alteraçöes menstruais (amenorréia secundária e oligoamenorréia) e infertilidade podem alertar o endocrinologista para o estabelecimento do diagnõsti-co definitivo da resistência ovariana ao LH ou ao FSH.
Subject(s)
Humans , Female , Infertility, Female/etiology , Receptors, FSH/deficiency , Receptors, LH/deficiency , Reproduction/physiology , Hypogonadism/etiology , Primary Ovarian Insufficiency/complicationsABSTRACT
A testotoxicose é uma forma rara da puberdade precoce familial em meninos com herança autossômica dominante. Os caracteres sexuais secundários ocorrem geralmente antes dos 4 anos de idade . Nesta condiçäo, níveis puberais de testosterona estäo associados a níveis suprimidos ou pré puberais de gonadotrofinas. Diversas mutaçöes ativadoras de linhagem germinativa no exon 11 do gene do receptor do LH têm sido descritas em meninos com testotoxicose. O estudo molecular de 8 meninos brasileiros com testotoxicose evidenciou 5 diferentes mutaçöes, sendo três delas identificadas exclusivamente no Brasil: Ala568Val, Leu457Arg e Leu368Pro, localizadas, respectivamente, na terceira alça intracelular e nas hélices transmembranosas III e I do receptor do LH. A mutaçäo Ala568Val foi identificada em 42,8 por cento da famílias brasileiras. Mulheres portadoras de mutaçöes ativadoras, mäes ou irmäs de meninos com testotoxicose, näo desenvolvem puberdade precoce e apresentam funçäo reprodutiva normal. Duas mulheres Brasileiras,incluindo uma menina em idade pré puberal, com mutaçöes ativadoras do receptor do LH eram assintomáticas e apresentaram perfil hormonal normal. Mutaçöes ativadoras somáticas do gene do receptor do LH foram recentemente identificados em 3 meninos com tumores das células de de Leydig. Contudo, um estudo recente nao evidenciou tais mutaçöes em 4 tumores de células de Leydig, 3 tecomas e 4 tumores de Sertoli-Leydig. Em conclusäo mutaçöes ativadoras germinativas e somáticas do gene do receptor do LH causam puberdade precoce e tumores das células de Leydig, respectivamente. Enquanto mutaçöes semelhantes no sexo feminino nao determinam fenótipo anormal.