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1.
Hum Reprod ; 25(4): 874-83, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20139427

ABSTRACT

BACKGROUND: The standard regimen of the levonorgestrel-only pill (1.5 mg either in a single dose or in a dose of 0.75 mg twice, 12 h apart) administered orally for emergency contraception (EC) has been shown to have no effect on endometrial development and markers of endometrial receptivity. We aimed to explore whether repeated oral and single vaginal administration of levonorgestrel affect the endometrium and thus potentially increase the EC efficacy, compared with the standard regimen. METHODS: Endometrial biopsies were taken from non-smoking, healthy women with proven fertility on cycle days LH + 6 to LH + 8 in control and levonorgestrel treatment cycles (each woman serving as her own control). Levonorgestrel was administered either orally (0.75 mg x 4, at 24 h intervals on LH + 1 to LH + 4; n = 8) or vaginally (a single dose of 1.5 mg on LH + 2; n = 7). Immunohistochemistry and real-time RT-PCR was performed to compare the levels of protein and mRNA for sex steroid receptors, interleukin-1beta, leukaemia inhibitory factor (LIF), vascular endothelial growth factor, cyclooxygenase-2, tumour necrosis factor-alpha, integrin alpha(v)beta(3) and mucin 1 in endometrial cells. RESULTS: Following the repeated oral treatment, the immunoreactivity of both progesterone receptor (PR)-A and PR-B declined in glandular epithelium (P = 0.03 and P = 0.02, respectively), whereas stromal immunoreactivity and mRNA expression of LIF increased compared with control (P < 0.001 and P = 0.03, respectively). However, vaginal levonorgestrel did not cause any significant endometrial changes. CONCLUSIONS: The two regimens of levonorgestrel caused either only minor or no alterations in markers of endometrial receptivity. New agents targeting the endometrial development should be explored in order to increase EC efficacy.


Subject(s)
Contraception, Postcoital/methods , Contraceptive Agents, Female/administration & dosage , Endometrium/drug effects , Endometrium/metabolism , Levonorgestrel/administration & dosage , Administration, Intravaginal , Administration, Oral , Adult , Biomarkers/metabolism , Female , Humans , Immunohistochemistry , Leukemia Inhibitory Factor/genetics , Leukemia Inhibitory Factor/metabolism , Luteinizing Hormone/urine , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Progesterone/genetics , Receptors, Progesterone/metabolism , Reverse Transcriptase Polymerase Chain Reaction
2.
Hum Reprod ; 24(7): 1612-8, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19359336

ABSTRACT

BACKGROUND: The increasing use of emergency contraceptive pills (ECPs) does not seem to reduce the number of induced abortions as would be expected, indicating that women use ECPs might also be a strong factor affecting their final efficacy. The study aimed to understand the attitude towards, and use of, ECPs among women seeking an abortion. METHODS: A cohort study was conducted via face-to-face questionnaire interview among women seeking abortion in Shanghai, China. Logistic regression analysis and chi(2) test were performed for statistical analysis. RESULTS: The response rate was 99.3%. Among all 5677 respondents aged 15-48 years, 48.8% were ECP ever-users. Compared with ever-users, ECP never-users were less likely to have used contraception during the present cycle of conception (P < 0.001). In response to the question on the main reason for non-use of contraception, ECP never-users were less likely to realize the risk of pregnancy and had less contraceptive knowledge (P < 0.001). Among 2773 ECP ever-users, 72.7% did not use ECPs to prevent the current pregnancy, mainly due to lack of awareness of pregnancy risk. Out of 757 women, 437 (57.7%) repeated unprotected sex after taking ECPs during the current pregnant cycle. A pharmacy was the preferred source to access ECPs, for the reason of convenience. CONCLUSIONS: Non-use of ECPs was correlated to less knowledge on fertility and a lower rate of contraceptive use among abortion-seeking women. Women of reproductive age should have access to ECPs and receive sufficient information on their use. Health care providers and pharmacists should also be trained in contraceptive counselling, including ECPs.


Subject(s)
Abortion, Induced/statistics & numerical data , Contraception, Postcoital/statistics & numerical data , Contraceptives, Postcoital/therapeutic use , Adolescent , Adult , China , Cohort Studies , Contraception Behavior , Family Planning Services/statistics & numerical data , Female , Health Education , Health Knowledge, Attitudes, Practice , Humans , Middle Aged , Pilot Projects , Pregnancy , Surveys and Questionnaires
3.
Hum Reprod ; 24(8): 1870-9, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19389793

ABSTRACT

BACKGROUND: Uterine leiomyomas are widely prevalent and frequently cause menorrhagia. The major therapeutic option today is hysterectomy. Medical options are of highest interest. METHODS: A total of 30 women with uterine leiomyomas scheduled for surgical intervention were randomized to receive either 50 mg mifepristone or placebo every other day during 3 months prior to surgery. Uterine blood flow and leiomyoma volume were evaluated once a month until surgery. Endometrial biopsies were obtained prior to and at end of treatment. Relevant biochemistry, symptoms and bleeding were recorded. Primary outcome was reduction in uterine leiomyoma size. RESULTS: There was a significant percentual decrease (P = 0.021) in the total leiomyoma volume in the mifepristone-treated group, -28 (-48, -8) % (mean +/- 0, 95 confidence interval), compared with the control group values 6 (-13, 25) %. Mifepristone treatment significantly reduced the bleeding days (P = 0.001) and increased serum haemoglobin values (P = 0.046). Serum cortisol levels remained unchanged, while a mild increase in serum androgens was noted. Endometrial biopsies showed no premalignant changes or changes in mitotic indices. CONCLUSION: Mifepristone may offer an effective treatment option for women with uterine leiomyoma and the associated pronounced uterovaginal bleeding. Clinical Trials identifier: www.clinicaltrials.gov: NCT00579475.


Subject(s)
Leiomyoma/drug therapy , Mifepristone/therapeutic use , Uterine Neoplasms/drug therapy , Adult , Double-Blind Method , Female , Hemoglobins/metabolism , Humans , Leiomyoma/pathology , Middle Aged , Regional Blood Flow/drug effects , Uterine Hemorrhage/drug therapy , Uterine Neoplasms/pathology , Uterus/blood supply
4.
Indian J Biochem Biophys ; 45(4): 244-9, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18788474

ABSTRACT

Thylakoid membranes were isolated and purified from diploid filamentous sporophytes of Porphyra yezoensis Ueda using sucrose density gradient ultracentrifugation (SDGUC). After thylakoid membranes were solubilized with SDS, the phtosystem II (PSII) particles with high 2, 6-dichloroindophenol (DCIP) photoreduction activity were isolated by SDGUC. The absorption and fluorescence spectra, DCIP photoreduction activity and oxygen evolution activity of the thylakoid membranes and PSII particles were determined. The polypeptide composition of purified PSII particles was distinguished by SDS-PAGE. Results showed that PSII particles of sporophytes differed from the gametophytes in spectral properties and polypeptide composition. Apart from 55 kDa D1-D2 heterodimer, CP47, CP43, 33 kDa protein, D1, D2, cyt b559 and 12 kDa protein were identified from PSII particles from sporophytes; a new 102 kDa protein was also detected. However, cyt c-550, 20 kDa, 14 kDa and 16 kDa proteins found in PSII particles from gametophytes were not detected in the sporophytes.


Subject(s)
Photosystem II Protein Complex , Porphyra/chemistry , Thylakoids/chemistry , 2,6-Dichloroindophenol/pharmacology , Dimerization , Electrophoresis, Polyacrylamide Gel , Molecular Weight , Photosystem II Protein Complex/chemistry , Photosystem II Protein Complex/isolation & purification , Photosystem II Protein Complex/metabolism , Sodium Dodecyl Sulfate/chemistry , Solubility , Spectrometry, Fluorescence , Thylakoids/metabolism , Ultracentrifugation
5.
Hum Reprod ; 22(11): 3031-7, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17890724

ABSTRACT

BACKGROUND: The use of fertility regulating drugs is limited among various socio-ethnic groups due to limited knowledge about their mechanism of action. This study investigates the effect of levonorgestrel and mifepristone on attachment of human embryos to an in vitro endometrial construct. METHOD: Three-dimensional endometrial constructs were established by co-culturing early luteal phase human endometrial stromal and epithelial cells. Expression of endometrial receptivity markers in this construct were examined by immunohistochemistry. Effects of mifepristone and levonorgestrel on viability and attachment of human blastocysts were investigated. RESULTS: Endometrial constructs expressed the factors involved in endometrial receptivity: estrogen receptor, progesterone receptor, vascular endothelial growth factor, leukemia inhibitory factor, interleukin-1, COX-2, MUC-1 and integrin-alpha(V)beta(3). None of the 15 embryos cultured with mifepristone attached to the endometrial construct (P < 0.01), whereas 10/17 in control, and 6/14 in levonorgestrel, groups attached. The attachment was confirmed by the positive expression of cytokeratin 7 at the attachment site. CONCLUSION: Mifepristone inhibits blastocyst attachment. Levonorgestrel did not impair the attachment of human embryos to the in vitro endometrial construct. This model could be used to understand endometrial receptivity and embryo-endometrial dialog and to develop new fertility regulating substances.


Subject(s)
Blastocyst/drug effects , Cell Culture Techniques/methods , Endometrium/drug effects , Gene Expression Regulation , Levonorgestrel/pharmacology , Mifepristone/pharmacology , Adult , Blastocyst/cytology , Cells, Cultured , Coculture Techniques , Contraceptive Agents, Female/pharmacology , Female , Hormone Antagonists/pharmacology , Humans , Immunohistochemistry/methods , Trophoblasts/cytology
6.
Indian J Biochem Biophys ; 43(5): 284-8, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17133734

ABSTRACT

Astaxanthin, a high-value ketocarotenoid is mainly used in fish aquaculture. It also has potential in human health due to its higher antioxidant capacity than beta-carotene and vitamin E. The unicellular green alga Haematococcus pluvialis is known to accumulate astaxanthin in response to environmental stresses, such as high light intensity and salt stress. Carotenoid hydroxylase plays a key role in astaxanthin biosynthesis in H. pluvialis. In this paper, we report the characterization of a promoter-like region (-378 to -22 bp) of carotenoid hydroxylase gene by cloning, sequence analysis and functional verification of its 919 bp 5'-flanking region in H. pluvialis. The 5'-flanking region was characterized using micro-particle bombardment method and transient expression of LacZ reporter gene. Results of sequence analysis showed that the 5'-flanking region might have putative cis-acting elements, such as ABA (abscisic acid)-responsive element (ABRE), C-repeat/dehydration responsive element (C-repeat/DRE), ethylene-responsive element (ERE), heat-shock element (HSE), wound-responsive element (WUN-motif), gibberellin-responsive element (P-box), MYB-binding site (MBS) etc., except for typical TATA and CCAAT boxes. Results of 5' deletions construct and beta-galactosidase assays revealed that a highest promoter-like region might exist from -378 to -22 bp and some negative regulatory elements might lie in the region from -919 to -378 bp. Results of site-directed mutagenesis of a putative C-repeat/DRE and an ABRE-like motif in the promoter-like region (-378 to -22 bp) indicated that the putative C-repeat/DRE and ABRE-like motif might be important for expression of carotenoid hydroxylase gene.


Subject(s)
Chlorophyta/enzymology , Chlorophyta/genetics , Mixed Function Oxygenases/biosynthesis , Mixed Function Oxygenases/genetics , Promoter Regions, Genetic , Base Sequence , Binding Sites , Cloning, Molecular , Gene Deletion , Lac Operon , Molecular Sequence Data , Mutagenesis, Site-Directed , Mutation , Plasmids/metabolism
7.
Zhonghua Zhong Liu Za Zhi ; 10(3): 200-4, 1988 May.
Article in Chinese | MEDLINE | ID: mdl-3219980

ABSTRACT

Thermography is a noninvasive technic of examination. Liquid-Crystal Thermography and Infrared Thermography have provided great help in the general survey of breast diseases during the past twenty years but not without some limitations. Recently, by applying the microwave technic clinically, progress has been made to measure minute temperature changes in the deeper tissues. Differential diagnosis of breast disease is possible by statistical calculating the temperature difference of the two breasts. A prospective study was done in 96 women who had both X ray mammography and digital noninvasive microwave thermography. 70/96 were proved by pathology. In this group of patients, the accuracy rate was 70.00% for digital microwave thermography, 81.82% for X ray mammography and 95.50% for the two combined. The false positive rates and false negative rates, advantages, disadvantages and the for general survey of breast disease of the digital microwave thermography discussed.


Subject(s)
Breast Diseases/diagnosis , Breast Neoplasms/diagnosis , Microwaves , Thermography/methods , Adenofibroma/diagnosis , Adolescent , Adult , Aged , Female , Fibrocystic Breast Disease/diagnosis , Humans , Middle Aged , Prospective Studies
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