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1.
Fertil Steril ; 97(2): 469-76, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22289288

ABSTRACT

OBJECTIVE: To obtain insight into the effects of androstenedione on ovarian folliculogenesis and oogenesis. DESIGN: Experimental study. SETTING: St. Marianna University School of Medicine. ANIMAL(S): Prepubertal (14-day-old) BDF1 female mice. INTERVENTION(S): Early secondary follicles were isolated from the ovaries and were cultured individually in vitro with or without androstenedione (10(-11) to 10(-5) M) for 12 days. Thereafter, the follicles were treated with hCG and epidermal growth factor (EGF). MAIN OUTCOME MEASURE(S): Diameters and morphology of follicles and oocytes; E(2) and P secretion; and chromatin configuration and expression of growth differentiation factor 9 (GDF9) in oocytes were examined. RESULT(S): Early secondary follicles developed to the preovulatory stage. Androstenedione treatments increased the follicle diameters, reduced survival rates of follicles, and promoted the formation of follicles with abnormal morphology, including misshapen oocyte. The secretion of E(2) and P was significantly higher in androstenedione-exposed follicles. Androstenedione prevented the alteration in chromatin configuration and reduced oocyte GDF9 expression. When follicles cultured with androstenedione were treated with hCG and EGF, the first polar body exclusion, chromosome alignment on metaphase plate, and spindle assembly were inhibited in the oocytes. CONCLUSION(S): These results demonstrate that excess androgen induces abnormalities in the morphology and function of developing oocytes, which impairs oocyte meiotic competence.


Subject(s)
Androstenedione/toxicity , Meiosis/drug effects , Oocytes/drug effects , Oogenesis/drug effects , Ovarian Follicle/drug effects , Animals , Cell Shape/drug effects , Cell Survival/drug effects , Cells, Cultured , Chorionic Gonadotropin/pharmacology , Chromatin Assembly and Disassembly/drug effects , Dose-Response Relationship, Drug , Epidermal Growth Factor/pharmacology , Estradiol/metabolism , Female , Growth Differentiation Factor 9/metabolism , Mice , Oocytes/metabolism , Oocytes/pathology , Ovarian Follicle/metabolism , Ovarian Follicle/pathology , Progesterone/metabolism , Time Factors
2.
Nagoya J Med Sci ; 73(3-4): 187-95, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21928700

ABSTRACT

The Japan Multi-Institutional Collaborative Cohort Study (J-MICC Study) is a long-term cohort study to investigate the interactions among genotypes, lifestyles, and lifestyle-related diseases, especially cancer. This article reports the outline of the baseline survey of the Daiko Study, one site of the J-MICC Study. That survey was conducted between June 9, 2008 and May 31, 2010 at the Daiko Medical Center of Nagoya University in Nagoya, Japan. Subjects were registered residents of Nagoya City aged 35 to 69 years who had not participated in other J-MICC sites. Recruitment was mainly announced through leaflets distributed in mailboxes citywide, personal communications, and regional information, such as posters in public or commercial facilities. Participants provided blood plasma, serum, buffy coat, urine, and data on health check-ups. They also completed a self-reported questionnaire on lifestyle, disease history, family history, and for women, reproductive history. As of the end of September 2010, 4 out of 5172 registered participants had withdrawn from the study, leaving data from 5168 participants (1467 males and 3701 females) available for analysis. Mean age +/- standard deviation (SD) was 52.5 +/- 10.3 years. Current smokers accounted for 24.1% (n=354) of males and 6.9% (n=256) of females. Current drinkers included 74.9% (n=1099) of males and 45.9% (n=1699) of females. Lifestyle data and specimens were successfully collected to examine any associations among disease biomarkers, lifestyles, and genotypes.


Subject(s)
Data Collection , Life Style , Neoplasms/etiology , Adult , Aged , Alcohol Drinking/adverse effects , Cohort Studies , Cooperative Behavior , Female , Genotype , Humans , Male , Middle Aged , Smoking/adverse effects
3.
Rinsho Byori ; 51(3): 225-30, 2003 Mar.
Article in Japanese | MEDLINE | ID: mdl-12707995

ABSTRACT

The diagnosis of rheumatic diseases is primarily based on clinical symptoms and laboratory findings. However, diagnosis of rheumatic disease is often difficult because of the variations even in the same disease. Routine laboratory tests are valuable in detecting renal dysfunctions. In this review, the important auto-antibodies and inflammatory markers associated with rheumatic diseases are described. Further, their utility as diagnostic and prognostic tools, including their specificity, sensitivity and practical applications, is discussed.


Subject(s)
Rheumatic Diseases/diagnosis , Autoantibodies/analysis , Biomarkers , Prognosis
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