scholarly journals Plasticity in intrinsic excitability of hypothalamic magnocellular neurosecretory neurons in late-pregnant and lactating rats

2021 ◽  
Author(s):  
Michael R Perkinson ◽  
Rachael A Augustine ◽  
Gregory T Bouwer ◽  
Emily F Brown ◽  
Isaiah Cheong ◽  
...  
Keyword(s):  
Late Pregnancy ◽  
Intrinsic Excitability ◽  
Neuron Activity ◽  
Trpv1 Channels ◽  
Neurosecretory Neurons ◽  
Pregnancy And Lactation ◽  
Vasopressin Secretion ◽  
Vasopressin Neuron ◽  
Vasopressin Neurons ◽  
Spike Firing

Oxytocin and vasopressin secretion from the posterior pituitary gland are required for normal pregnancy and lactation. Oxytocin secretion is relatively low and constant under basal conditions but becomes pulsatile during birth and lactation to stimulate episodic contraction of the uterus for delivery of the fetus and milk ejection during suckling. Vasopressin secretion is maintained in pregnancy and lactation despite reduced osmolality (the principal stimulus for vasopressin secretion) to increase water retention to cope with the cardiovascular demands of pregnancy and lactation. Oxytocin and vasopressin secretion are determined by the action potential (spike) firing of magnocellular neurosecretory neurons of the hypothalamic supraoptic and paraventricular nucleus. In addition to synaptic input activity, spike firing depends on intrinsic excitability conferred by the suite of channels expressed by the neurons. Therefore, we analysed oxytocin and vasopressin neuron activity in anaesthetised non-pregnant, late-pregnant and lactating rats to test the hypothesis that intrinsic excitability of oxytocin and vasopressin neurons is increased in late pregnancy and lactation to promote oxytocin and vasopressin secretion required for successful pregnancy and lactation. Hazard analysis of spike firing revealed a higher incidence of post-spike hyperexcitability immediately following each spike in oxytocin neurons, but not in vasopressin neurons, in late pregnancy and lactation, which is expected to facilitate high frequency firing during bursts. Despite lower osmolality in late-pregnant and lactating rats, vasopressin neuron activity was not different between non-pregnant, late-pregnant and lactating rats, and blockade of osmosensitive ΔN-TRPV1 channels inhibited vasopressin neurons to a similar extent in non-pregnant, late-pregnant and lactating rats. Furthermore, supraoptic nucleus ΔN-TRPV1 mRNA expression was not different between non-pregnant and late-pregnant rats, suggesting that enhanced activity of ΔN-TRPV1 channels might maintain vasopressin neuron activity to increase water retention during pregnancy and lactation. Introduction

scholarly journals Plasticity in Intrinsic Excitability of Hypothalamic Magnocellular Neurosecretory Neurons in Late-Pregnant and Lactating Rats

2021 ◽  
Vol 22 (13) ◽  
pp. 7140
Author(s):  
Michael R. Perkinson ◽  
Rachael A. Augustine ◽  
Gregory T. Bouwer ◽  
Emily F. Brown ◽  
Isaiah Cheong ◽  
...  
Keyword(s):  
Late Pregnancy ◽  
Intrinsic Excitability ◽  
Neuron Activity ◽  
Trpv1 Channels ◽  
Neurosecretory Neurons ◽  
Pregnancy And Lactation ◽  
Vasopressin Secretion ◽  
Vasopressin Neuron ◽  
Vasopressin Neurons ◽  
Spike Firing

Oxytocin and vasopressin secretion from the posterior pituitary gland are required for normal pregnancy and lactation. Oxytocin secretion is relatively low and constant under basal conditions but becomes pulsatile during birth and lactation to stimulate episodic contraction of the uterus for delivery of the fetus and milk ejection during suckling. Vasopressin secretion is maintained in pregnancy and lactation despite reduced osmolality (the principal stimulus for vasopressin secretion) to increase water retention to cope with the cardiovascular demands of pregnancy and lactation. Oxytocin and vasopressin secretion are determined by the action potential (spike) firing of magnocellular neurosecretory neurons of the hypothalamic supraoptic and paraventricular nuclei. In addition to synaptic input activity, spike firing depends on intrinsic excitability conferred by the suite of channels expressed by the neurons. Therefore, we analysed oxytocin and vasopressin neuron activity in anaesthetised non-pregnant, late-pregnant, and lactating rats to test the hypothesis that intrinsic excitability of oxytocin and vasopressin neurons is increased in late pregnancy and lactation to promote oxytocin and vasopressin secretion required for successful pregnancy and lactation. Hazard analysis of spike firing revealed a higher incidence of post-spike hyperexcitability immediately following each spike in oxytocin neurons, but not in vasopressin neurons, in late pregnancy and lactation, which is expected to facilitate high frequency firing during bursts. Despite lower osmolality in late-pregnant and lactating rats, vasopressin neuron activity was not different between non-pregnant, late-pregnant, and lactating rats, and blockade of osmosensitive ΔN-TRPV1 channels inhibited vasopressin neurons to a similar extent in non-pregnant, late-pregnant, and lactating rats. Furthermore, supraoptic nucleus ΔN-TRPV1 mRNA expression was not different between non-pregnant and late-pregnant rats, suggesting that sustained activity of ΔN-TRPV1 channels might maintain vasopressin neuron activity to increase water retention during pregnancy and lactation.

Somatodendritic dynorphin release: orchestrating activity patterns of vasopressin neurons

2007 ◽  
Vol 35 (5) ◽  
pp. 1236-1242 ◽  
Author(s):  
C.H. Brown ◽  
V. Scott ◽  
M. Ludwig ◽  
G. Leng ◽  
C.W. Bourque
Keyword(s):  
Activity Patterns ◽  
Opioid Peptide ◽  
Neuron Activity ◽  
Endogenous Opioid ◽  
Endogenous Opioid Peptide ◽  
Axon Terminals ◽  
Vasopressin Receptors ◽  
The Central Nervous System ◽  
Vasopressin Neuron ◽  
Vasopressin Neurons

Most neurons in the central nervous system co-express peptides alongside their principal transmitter, yet the function of these peptides is largely unknown. Vasopressin neurons of the hypothalamic supraoptic nucleus and paraventricular nucleus contain among the highest concentrations of dynorphin found in the brain. Dynorphin, an endogenous opioid peptide, is co-localized in the same neurosecretory vesicles as vasopressin and is released alongside vasopressin from the dendrites and axon terminals of vasopressin neurons. We and others have shown that neuropeptide release from the soma and dendrites of vasopressin neurons activates vasopressin receptors and κ-opioid receptors to cause activity-dependent modulation of vasopressin neuron activity, and that this is essential for activity patterning in vasopressin neurons.

Expression of the long form of the prolactin receptor in magnocellular oxytocin neurons is associated with specific prolactin regulation of oxytocin neurons

2006 ◽  
Vol 290 (5) ◽  
pp. R1216-R1225 ◽  
Author(s):  
I. C. Kokay ◽  
P. M. Bull ◽  
R. L. Davis ◽  
M. Ludwig ◽  
D. R. Grattan
Keyword(s):  
Prolactin Receptor ◽  
Neuron Activity ◽  
Expression Change ◽  
Paraventricular Nuclei ◽  
Baseline Recording ◽  
Long Form ◽  
Pregnancy And Lactation ◽  
Vasopressin Neurons ◽  
Labeled Probe

Magnocellular neurons of the supraoptic (SON) and paraventricular nuclei (PVN) show considerable plasticity during pregnancy and lactation. Prolactin receptors (PRL-R) have been identified in both these nuclei. The aim of this study was to investigate the cell type(s) expressing mRNA for the long form of prolactin receptor (PRL-RL) and to determine whether patterns of expression change during pregnancy and lactation. In addition, we examined effects of prolactin on excitability of oxytocin and vasopressin neurons. Sections from brains of nonpregnant, pregnant, and lactating rats were hybridized with an 35S-labeled probe to label PRL-RL mRNA together with digoxigenin-labeled probes to detect either oxytocin or vasopressin mRNA. In the SON, PRL-RL mRNA was predominantly colocalized with oxytocin mRNA, with over 80% of oxytocin neurons positive for PRL-RL mRNA. Very few (<10%) vasopressin neurons expressed PRL-RL mRNA. In the PVN, PRL-RL mRNA was also predominantly found in oxytocin neurons, and the proportion of PRL-RL-positive oxytocin neurons increased significantly during pregnancy and lactation. As in the SON, relatively few vasopressin cells contained PRL-RL mRNA. For in vivo electrophysiology, nonpregnant rats were anesthetized, and then extracellular single neuron activity was recorded in identified oxytocin and vasopressin neurons. After a period of baseline recording, the effect of prolactin (1 μg icv) on firing rate was examined. Prolactin treatment of nonpregnant rats induced a significant decrease in firing rates of oxytocin neurons. There was no effect of prolactin on the activity of vasopressin neurons. Together, these data provide strong evidence that prolactin directly and specifically regulates activity of oxytocin neurons.

scholarly journals Interaction of late pregnancy and lactation in rats

Reproduction ◽  
1999 ◽  
Vol 115 (2) ◽  
pp. 341-347 ◽  
Author(s):  
T. R. Koiter ◽  
H. Moes ◽  
N. Valkhof ◽  
S. Wijkstra
Keyword(s):  
Late Pregnancy ◽  
Pregnancy And Lactation

ANALYSIS OF RIBOSOMES AND POLYSOMES DERIVED FROM RABBIT MAMMARY GLANDS DURING PREGNANCY AND LACTATION

1971 ◽  
Vol 49 (4) ◽  
pp. 667-NP ◽  
Author(s):  
I. D. HERRIMAN ◽  
G. D. BAIRD ◽  
JUDY M. BRUCE
Keyword(s):  
Electron Microscopy ◽  
Density Gradient ◽  
Gradient Analysis ◽  
Late Pregnancy ◽  
Sucrose Density Gradient ◽  
Mammary Glands ◽  
Pregnancy And Lactation

SUMMARY Whole-ribosome and polysome-enriched fractions were prepared from the mammary glands of rabbits during late pregnancy and lactation. The composition of the fractions was determined by sucrose density gradient analysis and electron microscopy. The range of size of polysomal aggregates was similar in the late-pregnant and lactating gland, with aggregates containing five to nine ribosomal units predominating. However, the amount of polysomes relative to monosomes was invariably found to increase after parturition. The greater portion of this increase was accounted for by the increased abundance of aggregates containing five to nine units.

Influence of temperature on maternity roost selection by noctule bats (Nyctalus noctula) and Leisler’s bats (N. leisleri) in Białowieża Primeval Forest, Poland

2006 ◽  
Vol 84 (6) ◽  
pp. 900-907 ◽  
Author(s):  
Ireneusz Ruczyński
Keyword(s):  
Late Pregnancy ◽  
Ground Level ◽  
Data Logger ◽  
Primeval Forest ◽  
Tree Cavities ◽  
Roost Selection ◽  
Pregnancy And Lactation ◽  
Maximum Temperatures ◽  
Białowieża Primeval Forest ◽  
Nyctalus Noctula

This study tests whether the temperature of tree cavities determines their selection by bats in Białowieża Primeval Forest (BPF), eastern Poland. Using a data logger, I simultaneously measured the temperature in cavities selected by bats as roosts and the temperature in available but unselected cavities. The maternity roosts chosen by noctule bats, Nyctalus noctula (Schreber, 1774), and Leisler’s bats, N. leisleri (Kuhl, 1817), during late pregnancy and lactation were warmer than unoccupied cavities, but temperature ranges in the two types of cavity did not differ. A logistic regression model showed that the mean cavity temperature during the night (2200–0400) and the minimum cavity temperature over a 24 h period were crucial for roost selection. This suggests that female noctule and Leisler’s bats selected roosts that promoted juvenile growth and used tree cavities that could save them energy while they were active because the cavity temperatures were close to the lower critical temperature of their thermoneutral zone. I also suggest that selection of warmer cavities minimized the bats' energy expenditure prior to emergence from the roost and that passive rewarming inside the cavity was an important factor in minimizing energetic costs of roosting by bats in BPF. Mean and maximum temperatures recorded near tree trunks increased with the height at which the temperature was measured (ground level, 10, 20, and 30 m), suggesting that bats can gain thermal benefits from insolation of the trunk by selecting highly placed cavities, as was observed in BPF.

scholarly journals Pregnancy- and lactation-associated osteoporosis with vertebral fractures: a systematic review

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Ying Qian ◽  
Lei Wang ◽  
Lili Yu ◽  
Weimin Huang
Keyword(s):  
Back Pain ◽  
Vertebral Fractures ◽  
Data Extraction ◽  
Treatment Options ◽  
Osteoporotic Fractures ◽  
Late Pregnancy ◽  
Mean Value ◽  
Thoracolumbar Region ◽  
Pregnancy And Lactation ◽  
Z Scores

Abstract Background To review, analyze and characterize the pregnancy and lactation-related osteoporosis (PLO) with vertebral fractures based on the extraction data in the previous studies. Methods A comprehensive literature search of electronic databases including the PubMed, Embase and Web of Science was conducted from January 1st,1990 to December 1st, 2020. The enrolled data were pooled to analyze the baseline characteristics, clinical features, risk factors and treatment options. Results A total of 65 articles with 338 cases were enrolled for data extraction. The enrolled cases aged from 19 to 47 years, with a mean value of 35.7 years old. The average body mass index (BMI) was 22.2 kg/m2 ranged from 16.0 to 39.0 kg/m2. Of the 173 cases, 149 cases with vertebral fractures occurred in the first pregnancy, 19 cases in the second pregnancy, four cases in the third pregnancy and one case in the fourth pregnancy. Up to 91.5% of the back pain occurred within the last 3 months of pregnancy and the first 3 months after delivery. The most involved vertebral levels were L2, L1 and T12 accounting for 32.6% of all the fractures. The average fracture numbers were 4.4 levels per patient. The lumbar Z-scores were mostly recorded with a mean value of − 3.2 ranged from − 7.8 to 0. Conclusions PLO with vertebral fractures is a rare clinical entity, which is more likely to occur in older and thinner pregnant women. Back pain is the clinical complaint and mostly occurs in the late pregnancy and early lactation periods. Most vertebral fractures appear in the first pregnancy but it can occur in any time of pregnancy. Thoracolumbar region is the mostly involved region. As compared with postmenopausal osteoporotic fractures, PLO usually has multiple levels fractures. Bisphosphonates are the most widely used treatment so far, however, many factors need to be taken into account to decide which drug to choose in PLO and further studies are necessary for clear recommendation in the future.

scholarly journals Expression of a hypomorphic Pomc allele alters leptin dynamics during late pregnancy

2020 ◽  
Vol 245 (1) ◽  
pp. 115-127 ◽  
Author(s):  
Hui Yu ◽  
Zoe Thompson ◽  
Sylee Kiran ◽  
Graham L Jones ◽  
Lakshmi Mundada ◽  
...  
Keyword(s):  
Fat Mass ◽  
Energy Homeostasis ◽  
Leptin Receptor ◽  
Late Pregnancy ◽  
Placental Development ◽  
Hypomorphic Mutation ◽  
Protein Levels ◽  
Maximal Arc ◽  
Hypothalamic Arcuate Nucleus ◽  
Pregnancy And Lactation

Proopiomelanocortin (POMC) neurons in the hypothalamic arcuate nucleus (ARC) are essential for normal energy homeostasis. Maximal ARC Pomc transcription is dependent on neuronal Pomc enhancer 1 (nPE1), located 12 kb upstream from the promoter. Selective deletion of nPE1 in mice decreases ARC Pomc expression by 70%, sufficient to induce mild obesity. Because nPE1 is located exclusively in the genomes of placental mammals, we questioned whether its hypomorphic mutation would also alter placental Pomc expression and the metabolic adaptations associated with pregnancy and lactation. We assessed placental development, pup growth, circulating leptin and expression of Pomc, Agrp and alternatively spliced leptin receptor (LepR) isoforms in the ARC and placenta of Pomc∆1/∆1 and Pomc+/+ dams. Despite indistinguishable body weights, lean mass, food intake, placental histology and Pomc expression and overall pregnancy outcomes between the genotypes, Pomc ∆1/∆1 females had increased pre-pregnancy fat mass that paradoxically decreased to control levels by parturition. However, Pomc∆1/∆1 dams had exaggerated increases in circulating leptin, up to twice of that of the typically elevated levels in Pomc+/+ mice at the end of pregnancy, despite their equivalent fat mass. Pomc∆1/∆1dams also had increased placental expression of soluble leptin receptor (LepRe), although the protein levels of LEPRE in circulation were the same as Pomc+/+ controls. Together, these data suggest that the hypomorphic Pomc∆1/∆1 allele is responsible for the perinatal super hyperleptinemia of Pomc∆1/∆1 dams, possibly due to upregulated leptin secretion from individual adipocytes.

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