Changes in postprandial release patterns of gastrointestinal hormones in late pregnancy and the early postpartum period

Author(s):  
TROND G. JENSSEN ◽  
HANNE H. HAUKLAND ◽  
BARTHOLD VONEN ◽  
JON FLORHOLMEN ◽  
PER G. BURHOL ◽  
...  
2014 ◽  
Vol 81 (4) ◽  
pp. 639-643 ◽  
Author(s):  
M. Bazzano ◽  
C. Giannetto ◽  
F. Fazio ◽  
S. Marafioti ◽  
E. Giudice ◽  
...  

2001 ◽  
Vol 168 (2) ◽  
pp. 257-262 ◽  
Author(s):  
M Kondo ◽  
M Kondo ◽  
T Udono ◽  
WZ Jin ◽  
WZ Jin ◽  
...  

Plasma concentrations of inhibin A and inhibin B during pregnancy and early lactation in chimpanzees were determined by enzyme-linked immunosorbent assay (ELISA). Plasma samples were taken from five pregnant chimpanzees at 6-9, 10, 20 and 25 weeks of pregnancy, and following parturition. Throughout pregnancy and the early postpartum period, circulating inhibin A and inhibin B concentrations remained low, at similar levels to those during the normal menstrual cycle in chimpanzees. Concentrations of inhibin A in the placental homogenate were high enough to be measured by the ELISA and by bioassay, whereas circulating inhibin bioactivities in late pregnancy were too low to be measured. Plasma concentrations of FSH remained low with no significant changes throughout pregnancy and the postpartum period. Plasma concentrations of oestradiol-17beta and progesterone at 25 weeks of pregnancy were much higher than normal menstrual cycle levels. It was concluded that in chimpanzees the levels of circulating inhibin A and inhibin B remained low throughout pregnancy and the early postpartum period, and that the concentrations of bioactive dimeric inhibin did not increase towards the end of pregnancy. The suppression of circulating FSH levels during pregnancy is suggested to be controlled by steroid hormones that increased significantly in late pregnancy, and the present findings further suggest that the secretory pattern and role of inhibin during pregnancy in chimpanzees may be different from that in human and other primates.


1993 ◽  
Vol 48 (3) ◽  
pp. 355-363 ◽  
Author(s):  
Vicente Barrios ◽  
Lillian Puebla ◽  
Maria Nelly Rodriguez-Sanchez ◽  
Eduardo Arilla

2018 ◽  
Vol 243 (15-16) ◽  
pp. 1220-1232 ◽  
Author(s):  
Megan E Parrott ◽  
Esam Aljrbi ◽  
Diane L Biederman ◽  
Ryan N Montalvo ◽  
Jeremy L Barth ◽  
...  

Pregnancy creates a condition of cardiac volume overload which leads to physiological eccentric hypertrophy of the heart that is reversed in the postpartum period. Pathological cardiac changes in non-pregnant animals are associated with extracellular matrix remodeling. Based on preliminary microarray findings in the hearts of non-pregnant, pregnant, and postpartum mice, we hypothesized that changes in the expression of extracellular matrix protein genes would accompany functional changes in the heart that occur with reproductive status. Adult left ventricle parameters were evaluated by echocardiography in C57BL/6 mice at diestrous (virgin), and at pregnancy days (eds) 10, 12, and 18/19, and at postpartum days (ppds) 1.5 and 7. Twenty-one left ventricle mRNAs were evaluated including genes for tissue inhibitor of metalloproteinases (Timps), several matrix metallopeptidases (Mmps), collagens (Cols), proteoglycans, and enzymes involved in matrix remodeling at similar days except ed10. Compared to virgin mice, left ventricle internal diameter during diastole and end diastolic volumes significantly increased at ed12, ed18/19, ppd1.5, and ppd7. Left ventricle internal diameter during systole was increased at ed18/19 and ppd1.5, and end systolic volume was increased at ed18/19 compared to virgin mice. Timp1 mRNA levels were higher in late pregnancy and the early postpartum period, and Timp2-4 mRNAs levels were lower at one or both postpartum days compared to specific earlier time points. Mmp3 mRNA levels were higher during late pregnancy and postpartum than earlier in pregnancy. Mmp13 mRNA level was lower at ppd1.5 than late pregnancy, and Mmp15 mRNA level was lowest at ppd7 compared to all other time points. Col1a1 and Col3a1 increased with pregnancy and stayed elevated through ppd7. Col8a1 mRNA was increased on both postpartum days compared to late pregnancy. Our results indicate that late pregnancy and the first week of the postpartum period are an active time for altered expression of extracellular matrix protein genes. Impact statement This study provides the first comprehensive analysis of extracellular matrix protein (ECM) gene expression combined with echocardiographic analyses of heart functional parameters in the murine heart during pregnancy and the early postpartum period. Our findings show regulation of all Timp, selected Mmps, and Col1a1, Col3a1, and Col8a1 mRNA levels with reproductive status, with the greatest number of significant changes occurring in the early postpartum period. Left ventricle cardiac diastolic parameters were the first to change during pregnancy and remained elevated postpartum, whereas systolic parameters were increased in late pregnancy and began to recover during the first week postpartum. These novel findings indicate that although some ECM genes are elevated during late pregnancy, that the postpartum period is a time of robust altered ECM gene expression. These studies provide a basis for examining ECM proteins and their activities in the normal pregnant and postpartum heart and in models of postpartum cardiomyopathy.


2015 ◽  
Vol 100 (8) ◽  
pp. 3159-3164 ◽  
Author(s):  
Alberto Moreno Zaconeta ◽  
Angélica Amorim Amato ◽  
Gustavo Barcelos Barra ◽  
Lucília Domingues Casulari da Motta ◽  
Vinícius Carolino de Souza ◽  
...  

Context: CRH participates in the hypothalamic-pituitary-adrenal axis and in neural circuits involved in the pathophysiology of depression. During pregnancy, the placenta produces large amounts of CRH, and production ceases abruptly after delivery. The relationship between CRH in the cerebrospinal fluid (CSF) during pregnancy and peripartum mood disorders has not been investigated. Objectives: The objectives were to determine whether there are differences in CSF CRH concentrations of pregnant and nonpregnant women and whether CSF CRH concentrations in late pregnancy are associated with the presence of depressive symptoms during pregnancy and in the early postpartum period. Design: This was a prospective cohort study conducted from January to April, 2011. Setting: The study was conducted in one public and two private hospitals in Brasilia, Brazil. Patients: Patients included 107 healthy pregnant women who underwent elective cesarean delivery and 22 nonpregnant healthy women who underwent spinal anesthesia for elective surgical sterilization. Intervention: CRH in CSF was measured in pregnant and nonpregnant women by ELISA. Main Outcome Measure: The association between CSF CRH concentration at delivery and maternal depression assessed before cesarean section and postpartum (4 to 8 wk) with the Edinburgh Postnatal Depression Scale (EPDS), with a cutoff of ≥ 13. Results: CRH concentration in the CSF was significantly higher in pregnant (4.1 ± 0.51 log CRH) than in nonpregnant women (3.6 ± 0.26 log CRH) (P < .001). Depressive symptoms starting after delivery occurred in 5.6% of women. CRH concentration in CSF was not different between women without depressive symptoms and women showing such symptoms during pregnancy or in the postpartum period. Conclusion: CRH concentration in the CSF was higher in pregnant women than in nonpregnant women. However, in this sample, CSF CRH in late pregnancy was not associated with new-onset depressive symptoms in the early postpartum period.


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