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Current Advances in Oxytocin Research

A special issue of Current Issues in Molecular Biology (ISSN 1467-3045). This special issue belongs to the section "Biochemistry, Molecular and Cellular Biology".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 1867

Special Issue Editor


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Guest Editor
Department of Precision and Regenerative Medicine, School of Medicine, University of Bari Aldo Moro, P.za G. Cesare 11, 70100 Bari, Italy
Interests: oxytocin; thermoregulation; skeletal muscle; obesity; Prader–Willi syndrome
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Special Issue Information

Dear Colleagues,

The discovery of the pituitary neurohormone oxytocin led to the 1955 Nobel Prize in Chemistry being awarded to Vincent du Vigneaud. This represented the culmination of a research programme dating back to 1895, when Oliver and Schafer reported that a substance extracted from the pituitary gland elevates blood pressure when intravenously injected into dogs. Dale later reported on a neurohypophysial substance that triggers uterine contraction, stimulates lactation and functions in antidiuresis. Purification of the pituitary gland extracts revealed that the vasopressor and antidiuretic activity could be attributed to vasopressin, and the uterotonic and lactation-promoting activity could be attributed to oxytocin. In 1950, the amino acid sequences of vasopressin and oxytocin were determined, and both peptides were chemically synthesised. This revealed that vasopressin (CYFQNCPRG-NH2) and oxytocin (CYIQNCPLG-NH2) are structurally very similar, with only two amino acids differing, which is indicative of their common evolutionary origin and a disulphide bridge between the cysteine residues at positions 1 and 6 conserved in all vasopressin/oxytocin-type peptides. This characterisation and discovery of oxytocin led to the Nobel Prize being awarded to Vincent du Vigneaud in 1955. The common evolutionary origin of vasopressin and oxytocin, as indicated by their structural similarity, dates back to millions of years ago, which suggests that oxytocin has effects that go beyond uterine contractions and pregnancy. Nevertheless, such evidence was uncovered only 50 years after its discovery, in early 2000, when mice depleted of either oxytocin or its receptor were observed to develop late onset obesity and metabolic syndrome, thus establishing the involvement of oxytocin in the regulation of energy and metabolism. Interestingly, the metabolic phenotype of oxytocin and oxytocin receptor-deficient mice diverges in young versus older animals, taking time to reach full force, and is established in the absence of hyperphagia. The effects of oxytocin on fat and energy are both direct, since oxytocin is anorexigenic, and indirect, when oxytocin regulates the lean/fat mass composition in skeletal muscle, potentiating the slow twitch muscle as it does in the uterus. Finally, while oxytocin negatively modulates adipogenesis, peripheral oxytocin promotes osteoblast differentiation and function, leading to increased bone formation through the direct effect of oxytocin binding to its receptor on osteoblasts. Connecting the dots downstream of these findings, it appears that oxytocin acts on the three components of body composition: fat, muscle and bone. Evolutionarily, the anabolic effect of oxytocin makes sense since oxytocin concentrations increase during challenging situations, including pregnancy and lactation in mammals, and triggers aggressive behaviour that, in females, is important for the protection of offspring after labour, when they are most vulnerable to predators, and plasma oxytocin concentration is at its peak. From a wider perspective, this demonstrates that the effects of oxytocin are beneficial in the management of osteoporosis, body fat gain, diabetes, sarcopenia and all age-related diseases affecting elderly men and women, indicating the exciting therapeutic potential but also challenges, namely, to find a single route, dosage and schedule able to reach all the targets. Thus, let this be a mission that could be celebrated in 2055, i.e., the 100th anniversary of oxytocin’s discovery. As such, for this Special Issue, we invite all colleagues that have made significant contributions to studies relating to oxytocin in recent years to contribute with reviews or original research articles.

Dr. Claudia Camerino
Guest Editor

Manuscript Submission Information

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Keywords

  • oxytocin
  • thermoregulation
  • skeletal muscle
  • obesity
  • Prader–Willi syndrome

Published Papers (2 papers)

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Research

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14 pages, 1765 KiB  
Article
Oxytocin Exhibits Neuroprotective Effects on Hippocampal Cultures under Severe Oxygen–Glucose Deprivation Conditions
by Mara Ioana Ionescu, Ioana-Florentina Grigoras, Rosana-Bristena Ionescu, Diana Maria Chitimus, Robert Mihai Haret, Bogdan Ianosi, Mihai Ceanga and Ana-Maria Zagrean
Curr. Issues Mol. Biol. 2024, 46(6), 6223-6236; https://doi.org/10.3390/cimb46060371 - 19 Jun 2024
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Abstract
Perinatal asphyxia (PA) and hypoxic-ischemic encephalopathy can result in severe, long-lasting neurological deficits. In vitro models, such as oxygen–glucose deprivation (OGD), are used experimentally to investigate neuronal response to metabolic stress. However, multiple variables can affect the severity level of OGD/PA and may [...] Read more.
Perinatal asphyxia (PA) and hypoxic-ischemic encephalopathy can result in severe, long-lasting neurological deficits. In vitro models, such as oxygen–glucose deprivation (OGD), are used experimentally to investigate neuronal response to metabolic stress. However, multiple variables can affect the severity level of OGD/PA and may confound any measured treatment effect. Oxytocin (OXT) has emerged as a potential neuroprotective agent against the deleterious effects of PA. Previous studies have demonstrated OXT’s potential to enhance neuronal survival in immature hippocampal cultures exposed to OGD, possibly by modulating gamma-aminobutyric acid-A receptor activity. Moreover, OXT’s precise impact on develo** hippocampal neurons under different severities of OGD/PA remains uncertain. In this study, we investigated the effects of OXT (0.1 µM and 1 µM) on 7-day-old primary rat hippocampal cultures subjected to 2 h OGD/sham normoxic conditions. Cell culture viability was determined using the resazurin assay. Our results indicate that the efficacy of 1 µM OXT treatment varied according to the severity of the OGD-induced lesion, exhibiting a protective effect (p = 0.022) only when cellular viability dropped below 49.41% in non-treated OGD cultures compared to normoxic ones. Furthermore, administration of 0.1 µM OXT did not yield significant effects, irrespective of lesion severity (p > 0.05). These findings suggest that 1 µM OXT treatment during OGD confers neuroprotection exclusively in severe lesions in hippocampal neurons after 7 days in vitro. Further research is warranted to elucidate the mechanisms involved in OXT-mediated neuroprotection. Full article
(This article belongs to the Special Issue Current Advances in Oxytocin Research)
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19 pages, 481 KiB  
Review
The Role of Oxytocin in Polycystic Ovary Syndrome: A Systematic Review
by Nicoletta Cera, Joana Pinto and Duarte Pignatelli
Curr. Issues Mol. Biol. 2024, 46(6), 5223-5241; https://doi.org/10.3390/cimb46060313 - 25 May 2024
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Abstract
Polycystic Ovary Syndrome (PCOS) is the most common endocrine disorder that affects women of reproductive age, representing the primary cause of anovulatory infertility. The nonapeptide oxytocin (OT) plays an important role in cognitive, emotional, and reproductive functions in human beings. Oxytocin receptors are [...] Read more.
Polycystic Ovary Syndrome (PCOS) is the most common endocrine disorder that affects women of reproductive age, representing the primary cause of anovulatory infertility. The nonapeptide oxytocin (OT) plays an important role in cognitive, emotional, and reproductive functions in human beings. Oxytocin receptors are expressed in several body parts, including the ovaries. Despite this, the possible role played by oxytocin in symptoms of PCOS is not clear. The present systematic review aimed at understanding the presence of possible oxytocin level alterations in PCOS, the connection between alterations of OT levels and the symptoms of PCOS, and the effect of oxytocin administration in PCOS. After a systematic search in the principal databases, eight studies, five human and three animal, were included. Four human studies and one animal study highlighted the role played by oxytocin in fertility issues related to PCOS. Three human and two animal studies investigated the role of body weight and OT levels. Studies that analyzed oxytocin basal levels in women agreed that PCOS is associated with a reduction in the serum level of oxytocin. Two human studies and one animal study agreed about lower levels of oxytocin, confirming a possible implication of the dysfunction of OT in the pathogenesis of PCOS. Full article
(This article belongs to the Special Issue Current Advances in Oxytocin Research)
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