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2.
Br J Dermatol ; 161(4): 846-53, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19485999

ABSTRACT

BACKGROUND: Questionnaires are widely used in epidemiological studies to measure eczema symptom prevalence, but there are concerns regarding their accuracy if used as a diagnostic tool. OBJECTIVES: To compare the performance of a validated eczema symptom questionnaire and a standardized skin examination protocol employed in the second phase of the International Study of Asthma and Allergies in Childhood (ISAAC). METHODS: A total of 30,358 schoolchildren aged 8-12 years from 18 countries were examined for flexural eczema. Parents also completed an eczema symptom questionnaire. We compared prevalence estimates at the population level based on the questionnaire vs. physical examination. We also compared the skin examination and the ISAAC questionnaire in making a diagnosis of flexural eczema. RESULTS: The point prevalences for flexural eczema at centre level based on a single examination were lower than the questionnaire-based 12-month period prevalences (mean centre prevalence 3.9% vs. 9.4%). Correlation between prevalences of both outcome measures was high (r = 0.77, P < 0.001). At the individual level, questionnaire-derived symptoms of 'persistent flexural eczema in the past 12 months' missed < 10% of cases of flexural eczema detected on physical examination. However, between 33% and 100% of questionnaire-based symptoms of 'persistent flexural eczema in the past 12 months' were not confirmed on examination. CONCLUSIONS: ISAAC questionnaire-derived symptom prevalences are sufficiently precise for comparisons between populations. Where diagnostic precision at the individual level is important, questionnaires should be validated and potentially modified in those populations beforehand, or a standardized skin examination protocol should be used.


Subject(s)
Eczema/diagnosis , Physical Examination/standards , Surveys and Questionnaires/standards , Child , Eczema/epidemiology , Female , Germany/epidemiology , Humans , Male , Prevalence , Risk Factors , Severity of Illness Index
3.
Lung India ; 26(3): 86-8, 2009 Jul.
Article in English | MEDLINE | ID: mdl-20442843

ABSTRACT

With the object to strengthen the clinical status of tuberculous sarcoidosis, we present in this article, the case records published in internationally recognized journals by specialists. From review of clinical material, we have also formulated a table that defines diagnostic criteria of tuberculous sarcoidosis.

4.
Hum Reprod ; 18(9): 1797-801, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12923130

ABSTRACT

BACKGROUND: Insulin-like growth factor-1 (IGF-1) is known to play a role in ovarian follicular development augmenting the action of FSH. Low intrafollicular concentrations have been detected in women who respond poorly to gonadotrophins. This study addresses the relationship between serum IGF-1 levels following pituitary desensitization and ovarian response to gonadotrophin stimulation. METHODS: This is a case-control study of 78 patients undergoing IVF-embryo transfer treatment. Thirty-nine strictly-defined poor responder patients requiring 50 or more ampoules (75 IU FSH) to reach oocyte retrieval were compared with 39 age-matched normal responders, requiring fewer than 50 ampoules. IGF-1 concentrations were determined by extraction radioimmunoassay on serum samples obtained after pituitary desensitization but prior to gonadotrophin stimulation. RESULTS: Despite highly significant differences in measures of ovarian response between groups, the mean serum IGF-1 concentration was not statistically significantly different between poor and normal responders [(31.5 nmol/l [95% confidence interval (CI) 28.5-34.5] versus 34.5 nmol/l (95% CI 31.8-37.2)] respectively. No correlation between oocyte number or total gonadotrophin used and serum IGF-1 concentration was observed. CONCLUSION: Whilst IGF-1 influences ovarian follicular development this study suggests that serum IGF-1 does not predict ovarian response and does not differentiate between critically-defined poor and normal responders.


Subject(s)
Buserelin/therapeutic use , Fertility Agents, Female/therapeutic use , Fertilization in Vitro , Follicle Stimulating Hormone/therapeutic use , Ovary/drug effects , Pituitary Gland/drug effects , Receptor, IGF Type 1/metabolism , Adult , Case-Control Studies , Cell Count , Female , Humans , Oocytes , Osmolar Concentration , Pregnancy , Prognosis , Tissue and Organ Harvesting
5.
Asian J Androl ; 4(4): 273-9, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12508128

ABSTRACT

AIM: To investigate the effect of adrenalectomy (ADX) on the epididymidis of Sprague-Dawley rats. METHODS: The histological, biochemical (cholesterol protein, zinc, copper, alkaline and acid phosphatase aryl sulphatase, lactic dehydrogenase and leucine amino peptidase) and hormonal (FSH, LH and testosterone) changes of caput and cauda epididymis in ADX rats were observed. RESULTS: Organ wet weight, histological studies and morphometric measurements indicated a cellular degeneration in caput and cauda epididymis of ADX rats. Serum testosterone level was significantly lower in ADX than in sham-operated rats, while the serum FSH and LH were below the detection limit of 1 mIU/mL. The enzymatic activity was higher in ADX than in sham-operated rats. Epididymal zinc level increased whereas copper level decreased in ADX rats compared to the sham-operated. CONCLUSION: Adrenalectomy leads to degeneration of caput and cauda epididymidis epithelial cells as a result of decreased supply of testosterone.


Subject(s)
Adrenalectomy , Epididymis/physiology , Acid Phosphatase/metabolism , Alkaline Phosphatase/metabolism , Animals , Arylsulfatases/metabolism , Cholesterol/metabolism , Copper/metabolism , Epididymis/anatomy & histology , Epididymis/metabolism , Follicle Stimulating Hormone/blood , L-Lactate Dehydrogenase/metabolism , Leucyl Aminopeptidase/metabolism , Luteinizing Hormone/blood , Male , Organ Size , Rats , Rats, Sprague-Dawley , Reference Values , Testosterone/blood , Time Factors , Zinc/metabolism
6.
Asian J Androl ; 3(4): 289-300, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11753475

ABSTRACT

AIM: To study the effects of adrenalectomy and hydrocortisone on the ventral prostate of SD rats. METHODS: In adrenalectomised (ADX) and ADX + hydrocortisone (1, 2, or 4 mg) treated rats, the prostatic histology and the cholesterol, protein, zinc, and copper levels and the enzymic profile (acid phosphatase, alkaline phosphatase, aryl sulphatase, lactic dehydrogenase, and leucine aminopeptidase) in the prostatic tissue were determined; the serum hormonal profile (testosterone, FSH and LH) was also assayed. RESULTS: Adrenalectomy caused a progressive degeneration in prostatic structure that was not reversed by hydrocortisone treatment. The serum testosterone were significantly lower in ADX than in sham operated rats and lower in ADX + hydrocortisone than in ADX-C rats (P < 0. 01). The serum FSH and LH were below the detection limit of 1 mIU/mL. The enzymatic activity was higher in ADX than in sham operated rats and higher in ADX + hydrocortisone than in ADX-C rats (P < 0.05-0.01). The prostatic zinc levels were significantly higher in sham operated than in ADX, and higher in ADX-C than in ADX + hydrocortisone rats (P < 0.05-0.01). The prostatic copper level was significantly lower in sham operated than in ADX, and lower in ADX-C than in the ADX + hydrocortisone rats (P < 0.01). CONCLUSION: In rats, adrenalectomy leads to pathological and functional changes of the prostate. Hydrocortisone treatment at the doses employed did not reverse these changes.


Subject(s)
Adrenalectomy/adverse effects , Hydrocortisone/pharmacology , Prostate/drug effects , Prostate/pathology , Animals , Cholesterol/metabolism , Copper/metabolism , Follicle Stimulating Hormone/blood , Luteinizing Hormone/blood , Male , Prostate/enzymology , Prostate/metabolism , Proteins/metabolism , Rats , Rats, Sprague-Dawley , Testosterone/blood , Zinc/metabolism
7.
Am J Reprod Immunol ; 46(4): 280-7, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11642677

ABSTRACT

BACKGROUND: About 90% of cervical cancers and advanced cervical intraepithelial neoplasia (CIN II/III) are squamous epithelial cells with mRNA for human papillomavirus (HPV)16 and 18 and up-regulated epidermal growth factor receptor (EGF-R). Since presence of proteins rather than mRNA may be truly indicative of active infection or disease progression, establishing reliable methods for quantifying these proteins in cervical biopsies is important. METHOD: We have established an objective semi-quantitative immunofluorescent antibody assay to reliably assess the levels of HPV-E6/E7 and EGF-R proteins in the cervical biopsies from 12 normal women, five women with CIN I, 15 with CIN II/III and ten with cervical cancer. RESULTS: HPV-E6/E7 and EGF-R, when present, were specific to para-basal, basal and squamous epithelial cells (negative in stromal cells). Nine of ten women with cervical cancer and 15 (14 CIN II/III; 1 CIN I) of 20 women with CIN were positive for HPV-E6/E7. All 12 controls were HPV-negative. The controls and six women with CIN (four with CIN I) negative for HPV had low levels of EGF-R. The only exception was one woman with cervical cancer negative for HPV, with high levels of EGF-R. Levels of HPV-E6/E7 and EGF-R were significantly higher (P < 0.001 vs. controls) in women with advanced CIN II and III (P< 0.05 vs. controls in CIN I) and cervical cancer. The HPV-E6/E7 and EGF-R levels correlated significantly (r = 18.98; P < 0.001, by linear regression analysis). CONCLUSION: We have established a highly specific and sensitive semi-quantitative immunofluorescent antibody assay for measuring levels of HPV-E6/E7 proteins and EGF-R in archival cervical biopsies. Our data suggest an association between HPV-E6/E7 and EGF-R.


Subject(s)
Carcinoma, Squamous Cell/metabolism , DNA-Binding Proteins , ErbB Receptors/metabolism , Oncogene Proteins, Viral/metabolism , Papillomaviridae/metabolism , Repressor Proteins , Uterine Cervical Dysplasia/metabolism , Uterine Cervical Neoplasms/metabolism , Carcinoma, Squamous Cell/pathology , Cervix Uteri/metabolism , Cervix Uteri/pathology , Epithelial Cells/metabolism , Female , Fluorescent Antibody Technique, Indirect , Humans , Papillomavirus E7 Proteins , Uterine Cervical Neoplasms/pathology , Uterine Cervical Dysplasia/pathology
8.
Am J Reprod Immunol ; 44(4): 222-30, 2000 Oct.
Article in English | MEDLINE | ID: mdl-11076094

ABSTRACT

PROBLEM: To ascertain if cervical epithelial epidermal growth factor receptor (EGF-R) and serum insulin-like growth factor II (IGF-II) levels are potential markers for cervical cancer. METHOD OF STUDY: We tested cervical biopsies obtained from 18 controls, 3 women with cervical intraepithelial neoplasia (CIN) I, 17 women with CIN II and III, and 12 women with cervical cancer for EGF-R using a quantitative immunofluorescent antibody assay. We measured serum IGF-II levels using an enzyme-linked immunosorbent assay in 20 controls, 26 CIN patients, 12 with cervical cancer before therapy, 5 with cervical cancer for < 1 year, and 9 others > 1 year after therapy. RESULTS: The levels of cervical EGF-R in women with CIN and cervical cancer were significantly higher (P<0.05 for CIN I; P<0.001 for patients with CIN II and III or cervical cancer) than in controls. Women with cervical cancer (P<0.001 vs. controls) or advanced CIN (P = 0.03) had elevated levels of serum IGF-II, while the women with CIN I had levels similar to controls. Women with cervical cancer in the post-therapy period had significantly lower serum IGF-II levels than the women with cervical cancer before therapy (P<0.001). CONCLUSION: Cervical epithelial EGF-R and serum IGF-II levels may be used for the diagnosis and prognosis of cervical cancer.


Subject(s)
Biomarkers, Tumor/blood , Biomarkers, Tumor/metabolism , Cervix Uteri/metabolism , ErbB Receptors/metabolism , Insulin-Like Growth Factor II/metabolism , Uterine Cervical Neoplasms/blood , Uterine Cervical Neoplasms/metabolism , Case-Control Studies , Enzyme-Linked Immunosorbent Assay , Epithelial Cells/metabolism , Female , Fluorescent Antibody Technique/methods , Fluorescent Antibody Technique/standards , Humans , Prognosis , Quality Control , Uterine Cervical Neoplasms/diagnosis , Uterine Cervical Dysplasia/blood , Uterine Cervical Dysplasia/diagnosis , Uterine Cervical Dysplasia/metabolism
9.
Am J Reprod Immunol ; 44(2): 114-20, 2000 Aug.
Article in English | MEDLINE | ID: mdl-10994639

ABSTRACT

PROBLEM: Over-expression of epidermal growth factor-receptors (EGF-R) has been described in a variety of cancers, including cervical cancer. Nicotine may increase cellular proliferation rates through a mechanism involving EGF or EGF-R. In this study, we ascertain the effect of EGF antibodies on nicotine-enhanced proliferation rates in two cervical cancer cell lines. METHOD OF STUDY: We studied (a) nicotine-induced increase in the cellular expression of EGF-R in human papillomavirus (HPV)-positive ME-180 and HPV-negative HT-3 cervical cancer cell line cultures, using a semi-quantitative immunofluorescent antibody assay; (b) alterations in cellular proliferation in association with changes in EGF-R levels; and (c) the EGF-R mediation by EGF. RESULTS: Nicotine exposure at physiologically attainable plasma concentrations caused increased expression of EGF-R in both cervical cancer cell lines. Up-regulation of EGF-R was associated with increased cellular proliferation. Decreased expression of EGF-R was associated with decreased cellular proliferation. These data were consistent with EGF-R expression as a mechanism for the control of proliferation of the cervical cancer cells. The action of nicotine was abrogated when antibodies to EGF were added, implying that nicotine up-regulation of EGF-R may be mediated by EGF. CONCLUSIONS: Our data show that nicotine-induced proliferation of cervical cancer cells is mediated through EGF-R over-expression and that this action of nicotine utilizes EGF.


Subject(s)
Epidermal Growth Factor/physiology , ErbB Receptors/drug effects , Nicotine/pharmacology , Uterine Cervical Neoplasms/metabolism , Cell Division , ErbB Receptors/biosynthesis , Female , Humans , Tumor Cells, Cultured , Up-Regulation , Uterine Cervical Neoplasms/pathology
11.
Fertil Steril ; 73(5): 901-7, 2000 May.
Article in English | MEDLINE | ID: mdl-10785214

ABSTRACT

OBJECTIVE: To compare patient and cycle characteristics among three study groups: early ovarian hyperstimulation syndrome (OHSS), late OHSS, and non-OHSS. DESIGN: Prospective observational study. SETTING: University assisted conception service. PATIENT(S): Women undergoing in vitro fertilization, intracytoplasmic sperm injection or gamete intrafallopian transfer treatment at Bristol University In Vitro Fertilization Service between January 1, 1995, and December 31, 1998. INTERVENTION: None. MAIN OUTCOME MEASURE(S): Patient age, prevalence of polycystic ovaries, gonadotropin requirement, peak serum estradiol (E(2)) concentration, number of oocytes retrieved, clinical pregnancy rate, number of gestation sacs, and severity of OHSS. RESULT(S): Women with early OHSS had significantly higher serum E(2) levels and lower gonadotropin requirements than did the other groups. Cycles with either early or late OHSS had significantly more oocytes collected than those without OHSS. Serum E(2) and oocyte numbers did not accurately predict the risk of developing late OHSS. Clinical pregnancies occurred in all cycles with late OHSS, and multiple pregnancies were significantly more frequent in the late OHSS group than in the other groups. Late OHSS was more likely than early OHSS to be severe. CONCLUSION(S): Early OHSS relates to "excessive" preovulatory response to stimulation, whereas late OHSS depends on the occurrence of pregnancy, is likelier to be severe, and is only poorly related to preovulatory events.


Subject(s)
Ovarian Hyperstimulation Syndrome/pathology , Adult , Age Factors , Estradiol/blood , Female , Fertilization in Vitro/adverse effects , Humans , Middle Aged , Observation , Oocytes , Outcome Assessment, Health Care , Ovarian Hyperstimulation Syndrome/blood , Ovarian Hyperstimulation Syndrome/complications , Polycystic Ovary Syndrome/complications , Pregnancy , Prospective Studies , Risk Factors , Tissue and Organ Harvesting
12.
Fertil Steril ; 73(4): 825-30, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10731548

ABSTRACT

OBJECTIVE: To further elucidate cortisol metabolism in the follicular microenvironment at the time of oocyte retrieval, the presence of 11beta-hydroxysteroid dehydrogenase (HSD) messenger (m)RNA transcripts in oocytes; cumulus cells; granulosa cells; and CD45(+), CD15(+) leukocytes was assessed semiquantitatively. DESIGN: Controlled study using semiquantitative assessment of 11beta-HSD mRNA. SETTING: University IVF center. PATIENT(S): Twenty-six patients undergoing controlled ovarian hyperstimulation for assisted conception. INTERVENTION(S): Metaphase II oocytes; cumulus cells; granulosa cells, and CD45(+), CD15(+) leukocytes from individual follicular fluid aspirates. MAIN OUTCOME MEASURES: Semiquantitative analysis of PCR products after total RNA extraction and complementary DNA synthesis. RESULT(S): Periovulatory human oocytes; cumulus cells; CD45(+), CD15(+) leukocytes; and granulosa cells consistently express type 1 but not type 2 11beta-HSD mRNA. Expression of mRNA is greatest in cumulus cells. Type 1 11beta-HSD mRNA expression varies considerably in all cell types and among individual follicles and patients. CONCLUSION(S): These studies of mRNA expression suggest that the enzymes present both in and around the periovulatory oocyte will favor a high-cortisol environment.


Subject(s)
Hydroxysteroid Dehydrogenases/genetics , Leukocytes/enzymology , Oocytes/physiology , Ovary/cytology , 11-beta-Hydroxysteroid Dehydrogenases , Female , Fertilization in Vitro , Gene Expression Regulation , Glyceraldehyde-3-Phosphate Dehydrogenases/genetics , Granulosa Cells/metabolism , Humans , Isoenzymes/genetics , Leukocyte Common Antigens/metabolism , Lewis X Antigen/metabolism , Ovary/enzymology , Ovulation , Placenta/enzymology , Predictive Value of Tests , Pregnancy , Protein Tyrosine Phosphatase, Non-Receptor Type 1 , RNA, Messenger , Treatment Outcome
14.
Am J Kidney Dis ; 33(5): 917-9, 1999 May.
Article in English | MEDLINE | ID: mdl-10213649

ABSTRACT

The objective of this study is to evaluate the effect of chronic hemodialysis on serum progesterone level in pregnancy. Serum progesterone levels were measured predialysis and postdialysis using the radioimmunoassay technique in seven gravid women with renal failure requiring hemodialysis. Uterine contractions were measured before and after hemodialysis using home uterine activity monitoring (HUAM) in two patients. Thirty-three paired serum samples were obtained between 14 and 39 weeks' gestation. The mean change in serum progesterone level postdialysis throughout pregnancy ranged from -52.0% to +8.7% for each individual patient. The change in serum progesterone level was unrelated to gestational age. The woman experiencing the most significant decrease in serum progesterone level with dialysis continued her pregnancy to greater than 39 weeks. No significant increase in uterine contraction frequency was noted on HUAM postdialysis (P = 0.22), although both monitored patients experienced a small increase in serum progesterone levels. In conclusion, serum progesterone values showed a variable patient-specific response when measured predialysis and postdialysis in pregnancies complicated by renal failure. There was no significant increase in uterine activity noted postdialysis. Progesterone withdrawal does not appear to explain the increased frequency of preterm delivery in women after dialysis.


Subject(s)
Pregnancy Complications, Hematologic/blood , Progesterone/blood , Renal Dialysis , Renal Insufficiency/complications , Female , Gestational Age , Humans , Obstetric Labor Complications/etiology , Pregnancy , Renal Insufficiency/therapy , Time Factors
15.
Neurology ; 51(4): 1216-8, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9781567

ABSTRACT

We discuss a patient with sarcoidosis presenting with cranial neuropathy and a cerebral mass lesion evident on imaging. Also, we review from the literature six patients with sarcoidosis presenting with cerebral mass lesion. We emphasize the diagnostic role of Mantoux test site biopsy in patients with dominant or isolated neurologic presentation because the involved sites are not easily accessible and Kveim's test antigen is not commercially available.


Subject(s)
Brain Diseases/diagnosis , Oculomotor Nerve Diseases/diagnosis , Sarcoidosis/diagnosis , Biopsy , Brain Diseases/pathology , Granuloma/diagnosis , Granuloma/pathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Oculomotor Nerve Diseases/pathology , Parietal Lobe/pathology , Sarcoidosis/pathology
16.
Am J Primatol ; 45(3): 301-5, 1998.
Article in English | MEDLINE | ID: mdl-9651652

ABSTRACT

Platelet-activating factor (1-O-alkyl-2-acetyl-sn-glycero-3-phosphoryl-choline) (PAF) is a potent signaling phospholipid which has pleiotropic biological properties in addition to platelet activation. PAF has been detected in the spermatozoa in a number of species. The concentration of PAF is inversely related to human spermatozoa quality. There are no reports on the presence of PAF in nonhuman primate spermatozoa. Therefore, the primary objective of this study was to determine if PAF is present in the spermatozoa from the squirrel monkey (which is a seasonal breeder). A second objective was to determine if PAF levels change from the breeding to the nonbreeding season. Endogenous lipids were extracted from mature Bolivian squirrel monkeys (Saimiri boliviensis) spermatozoa and assayed for the presence of PAF by [125I] radioimmunoassay. PAF was detected in all samples assayed. PAF levels were significantly higher (P < 0.01) during the breeding season (mean: 3.58 ng/10(6) spermatozoa) than the nonbreeding season (mean: 0.76 ng/10(6) spermatozoa). The data demonstrate that PAF is present in squirrel monkey spermatozoa, with higher levels found during the breeding season. Additional studies are warranted to elucidate the role of PAF in spermatozoa function.


Subject(s)
Platelet Activating Factor/analysis , Saimiri/physiology , Spermatozoa/chemistry , Animals , Male , Reproduction/physiology , Seasons
17.
Indian J Exp Biol ; 36(1): 22-33, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9536647

ABSTRACT

Administration of glucocorticoid (1, 2 and 4 mg) in excess leads to degeneration of epididymides as supported by cellular degeneration, sperm density and morphometric measurements. Zinc level increased statistically after 1, 2 and 4 mg hydrocortisone treatment while copper increased after 1 and 2 mg treatment. Cholesterol, protein and leucine aminopeptidase levels increased and decreased significantly in caput and cauda respectively. Activity of alkaline phosphatase reduced significantly while the treatment of hydrocortisone at different doses elevated acid phosphatase, aryl sulphatase and lactate dehydrogenase activities. Evidently, these changes are as a result of onset of cellular degeneration leading to impairment of metabolic/secretory activity of epididymal cells. The possible involvement of pituitary-testis axis in hydrocortisone induced epididymal degeneration and functional inhibition has been discussed.


Subject(s)
Epididymis/drug effects , Epididymis/metabolism , Hydrocortisone/toxicity , Acid Phosphatase/metabolism , Alkaline Phosphatase/metabolism , Animals , Arylsulfatases/metabolism , Copper/metabolism , Epididymis/pathology , L-Lactate Dehydrogenase/metabolism , Leucyl Aminopeptidase/metabolism , Male , Rats , Rats, Sprague-Dawley , Zinc/metabolism
19.
J Cardiovasc Pharmacol ; 29(3): 311-5, 1997 Mar.
Article in English | MEDLINE | ID: mdl-9125667

ABSTRACT

Thromboxane A2 (TXA2) has been implicated as an important mediator of cardiovascular diseases. Aortas obtained from male rats are more sensitive to TXA2 mimetics compared with those obtained from females. A similar phenomenon has been reported in canine coronary arteries. To determine whether there is a gender-related difference in the regulation of TXA2 receptors by androgenic steroids, we determined the effect of testosterone and dihydrotestosterone (DHT) on TXA2 receptor density in cultured rat aortic smooth-muscle (RASM) cells and guinea pig coronary artery smooth-muscle (CASM) cells. TXA2 receptor density (B(max)) and dissociation constant (Kd) were determined by radioligand binding studies with (125)I-BOP, a TXA2 receptor agonist. Testosterone significantly (p < 0.05) increased TXA2 receptor density in cultured RASM cells and guinea pig CASM cells. DHT significantly (p < 0.005) increased the B(max) in male RASM cells (62 +/- 2 vs. 40 +/- 3 fmol/mg protein; n = 7; p < 0.005). DHT increased the B(max) values in both male and female RASM cells, but the increase was significantly (p < 0.05) less in female than in male RASM cells (57 +/- 10% increase for male and 31 +/- 5% for female). Androgen-receptor protein was detected in RASM cells by Western blot and was less in the female RASM cells than in the male. The results indicate that RASM cells possess an androgen receptor and that gender-related differences exist in the regulation of expression of TXA2 receptors by androgens.


Subject(s)
Androgens/pharmacology , Aorta/drug effects , Muscle, Smooth, Vascular/drug effects , Receptors, Thromboxane/drug effects , Sex Characteristics , Androgens/physiology , Animals , Aorta/physiology , Binding Sites , Cells, Cultured , Coronary Vessels/drug effects , Coronary Vessels/physiology , Dihydrotestosterone/pharmacology , Female , Guinea Pigs , Immunoblotting , In Vitro Techniques , Male , Muscle, Smooth, Vascular/physiology , Radioligand Assay , Rats , Receptors, Androgen/blood , Receptors, Androgen/drug effects , Receptors, Androgen/physiology , Receptors, Thromboxane/blood , Receptors, Thromboxane/physiology , Seminal Vesicles/drug effects , Testosterone/pharmacology
20.
Hum Reprod ; 12(12): 2629-34, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9455826

ABSTRACT

This review examines recent evidence suggesting a role for the immune system, in particular cytokines, in the pathogenesis of ovarian hyperstimulation syndrome (OHSS). Ovarian tissue is known to contain cells capable of producing a range of immunological mediators and the concentrations of these have been shown to be elevated in serum and ascitic fluid from women with established OHSS. Available evidence points to a role for vascular endothelial growth factor and interleukin-2, possibly acting through other intermediary cytokines, in the pathogenesis of OHSS. However, each individual has a unique cytokine profile and several cytokines may share biological actions, making it difficult to interpret data on isolated cytokine concentrations from relatively small numbers of patients. Improved understanding of the role of the immune system in the development of OHSS may have implications for the prediction, prevention and management of this iatrogenic condition.


Subject(s)
Ovarian Hyperstimulation Syndrome/immunology , Cytokines/immunology , Endothelial Growth Factors/physiology , Female , Humans , Lymphokines/physiology , Ovarian Hyperstimulation Syndrome/diagnosis , Ovarian Hyperstimulation Syndrome/prevention & control , Ovarian Hyperstimulation Syndrome/therapy , Vascular Diseases , Vascular Endothelial Growth Factor A , Vascular Endothelial Growth Factors
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