Oxytocin, the Love Hormone, in Stem Cell Differentiation DOI Creative Commons
Luca Pampanella, Giovannamaria Petrocelli,

Federica Forcellini

и другие.

Current Issues in Molecular Biology, Год журнала: 2024, Номер 46(11), С. 12012 - 12036

Опубликована: Окт. 25, 2024

Oxytocin (OXT) is a neurohypophysial nonapeptide that exerts its effects mainly through the oxytocin receptor (OXTR). Several studies have pointed out role of OXT in modulation stem cell (SC) fate and properties. SCs are undifferentiated cells characterized by remarkable ability to self-renew differentiate into various types body. In this review, we focused on SC differentiation. Specifically, summarize discuss scientific research examining mesodermal SC-derived lineages, including cardiac, myogenic, adipogenic, osteogenic, chondrogenic The available related differentiation provide little insights about molecular mechanism mediated OXT–OXTR pathway. Further needed fully elucidate these pathways effectively modulate develop potential therapeutic applications regenerative medicine.

Язык: Английский

Hypophysectomy, pituitary neuroadenolysis and pituitary radiosurgery for the treatment of refractory cancer pain: a historical review and mechanism investigation DOI Creative Commons
Yu‐Chen Hu,

Wanghao Zhang,

Zijian Chen

и другие.

Frontiers in Neurology, Год журнала: 2025, Номер 15

Опубликована: Янв. 10, 2025

Refractory cancer pain affects 10-20% of patients with advanced malignancies and is not adequately controlled by opioids. The intrathecal therapy an effective interventional procedure for referral, but the implanted infusion pumps are costly refilling requires technical expertise. Hypophysectomy, in its three stages-surgical, chemical, radiosurgical-has emerged as alternative managing this pain. However, underlying mechanism remains elusive, existing hypotheses unable to comprehensively account both initial long-term analgesic effects. This literature review explores historical evolution, clinical outcomes, hypothesized mechanisms hypophysectomy relief. Surgical initially demonstrated 85.5% success rate carried significant risks like diabetes insipidus hypopituitarism. Chemical reduced invasiveness, achieving 75.1% relief fewer complications. Modern pituitary radiosurgery has improved safety while maintaining high efficacy (initial relief: 95.9%, long-term: 73.5%). remain unclear include tumor regression, increased β-endorphins, neuroendocrine modulation, hypothalamic involvement. A new hypothesis suggests that induces hormone redistribution (e.g., oxytocin, vasopressin) through hypothalamic-pituitary contributing immediate analgesia. Despite potential, unresolved issues such optimal radiation dose, assessment standardization, precise limit widespread adoption. underscores need larger, homogenous studies validate treating refractory These findings offer a promising avenue improving palliative care oncology.

Язык: Английский

Процитировано

0

The Role of Oxytocin Neurons in the Paraventricular Nucleus in Chronic-Sleep-Deprivation-Mediated Abnormal Cardiovascular Responses DOI Creative Commons
Yifei Zhang, Yuxin Wang,

Zhendong Xu

и другие.

Current Issues in Molecular Biology, Год журнала: 2025, Номер 47(4), С. 220 - 220

Опубликована: Март 25, 2025

Sleep disorders increase the risk of cardiovascular diseases. However, underlying mechanisms remain unclear. This study aims to examine critical role oxytocin neurons in paraventricular nucleus (PVNOXT) regulating system and elucidate potential through which sleep disturbance may contribute In this study, using an automated deprivation system, mice were given chronic (cSD) for 7 days, 6 h per day. cSD induced blood transcriptomic alterations accompanied by lower heart rate, higher pressure, elevated cardiac autophagy/apoptosis. Instant optogenetic activation provoked rate suppression normal mice, whereas precipitated intermittent arrest. On contrary, inhibition PVNOXT showed no influence on but it attenuated cSD-induced rise pressure. Long-term low-frequency stimulation (LTF) decreased neuronal excitability release, effectively reversing cSD-mediated responses. Mechanistically, triggered upregulation blood-derived 3-mercaptopyruvate sulfurtransferase (mPST), a postsynaptic activity certain extent. The quick long-term decrease LTF could lead feedback mPST expression thus reverse Altogether, modulation mediate abnormalities without affecting mice. Our research provided targets key diseases associated with disorders.

Язык: Английский

Процитировано

0

Oxytocin and autism: Insights from clinical trials and animal models DOI
Chuan Xing, Xiang Yu

Current Opinion in Neurobiology, Год журнала: 2025, Номер 92, С. 103015 - 103015

Опубликована: Март 30, 2025

Язык: Английский

Процитировано

0

Non-Peptidic Natural Products that Target and Modulate Oxytocin and Arginine Vasopressin Receptors: Opportunities and Challenges DOI Creative Commons

Dane F. L. Tregeagle,

Catherine Doherty,

Timothy B. Callis

и другие.

Journal of Pharmacological Sciences, Год журнала: 2025, Номер unknown

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Understanding peptide hormones: from precursor proteins to bioactive molecules DOI
Laetitia Coassolo, Amanda L. Wiggenhorn, Katrin J. Svensson

и другие.

Trends in Biochemical Sciences, Год журнала: 2025, Номер unknown

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

The impact of membrane receptors on modulating empathic pain DOI

Guilherme Pegas Teixeira,

Leandro Rocha, Robson Xavier Faria

и другие.

Neuropharmacology, Год журнала: 2025, Номер unknown, С. 110471 - 110471

Опубликована: Апрель 1, 2025

Язык: Английский

Процитировано

0

Novel Nonpeptide as Oxytocin Receptor Agonist DOI
Yinlong Li, Steven H. Liang

ACS Medicinal Chemistry Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 21, 2025

Язык: Английский

Процитировано

0

Oxytocin Analogues for the Oral Treatment of Abdominal Pain DOI Creative Commons
Thomas Kremsmayr,

Gudrun Schober,

Matthias Kaltenböck

и другие.

Angewandte Chemie International Edition, Год журнала: 2024, Номер unknown

Опубликована: Окт. 10, 2024

Abdominal pain presents an onerous reality for millions of people affected by gastrointestinal disorders such as irritable bowel syndrome (IBS) and inflammatory diseases (IBD). The oxytocin receptor (OTR) has emerged a new analgesic drug target with OTR expression upregulated on colon-innervating nociceptors in chronic visceral hypersensitivity states, accessible via luminal delivery. However, the low stability OTR's endogenous peptide ligand (OT) is bottleneck therapeutic development. Here, we report development potent fully gut-stable OT analogues, laying foundation area oral gut-specific therapeutics. Ligand optimisation guided structure-gut-stability-activity relationships yielded highly stable analogues (t

Язык: Английский

Процитировано

0

Oxytocin Analogues for the Oral Treatment of Abdominal Pain DOI Creative Commons
Thomas Kremsmayr,

Gudrun Schober,

Matthias Kaltenböck

и другие.

Angewandte Chemie, Год журнала: 2024, Номер unknown

Опубликована: Окт. 10, 2024

Abstract Chronische Bauchschmerzen stellen für Millionen von Menschen, die an gastrointestinalen Erkrankungen wie dem Reizdarmsyndrom und entzündlichen Darmerkrankungen leiden, eine schwere Belastung dar. Der Oxytocin Rezeptor (OTR) ist ein neues therapeutisches Wirkstoffziel Entwicklung Schmerzmittel: bei chronischer viszeraler Hypersensitivität Expression OTR auf vom Lumen aus zugänglichen Nozizeptoren im Dickdarm erhöht, was gezielte luminale Verabreichung Liganden ermöglicht. Allerdings stellt geringe gastrointestinale Stabilität des endogenen Peptidliganden (OT) Problem therapeutische In dieser Studie, beschreiben wir potenter verdauungsstabiler OT‐Verbindungen, den Grundstein neue Wirkstoffklasse oralen, darmspezifischen Peptidtherapeutika legen. Die Ligandenoptimierung, geleitet Struktur‐Verdauungsstabilitäts‐Aktivitäts‐Beziehungen, ergab stabile Verbindungen (t 1/2 >24 h, Vergleich zu t <10 min OT in Darmflüssigkeit), equipotent (~3 nM) waren verbesserte OTR‐Selektivität aufwiesen. rektale der besten Leitverbindung zeigte konzentrationsabhängig schmerzstillende Effekte einem chronischen Bauchschmerz Mausmodel. Auch orale signifikante analgetische Effekte. entwickelten angewandten Strategien könnten Weg Klasse oraler, darmspezifischer Peptide ebnen, um chronische erforschen bekämpfen – Bereich mit erheblichem ungedecktem medizinischem Bedarf.

Процитировано

0

Oxytocin/Oxytocin Receptor Signalling in the Gastrointestinal System: Mechanisms and Therapeutic Potential DOI Open Access
Huiping Liu, Gangqiang Yang,

Hongbo Wang

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(20), С. 10935 - 10935

Опубликована: Окт. 11, 2024

The neuropeptide hormone oxytocin (OT) is involved in various physiological and pathological processes via the receptor (OTR). While OT most widely known as a reproductive system nervous neurotransmitter, OT/OTR has gradually gained much attention for its role gastrointestinal (GI) system, such GI motility, secretion, bowel inflammatory reactions. Its importance cancers also been reported past few decades. promising clinical observations have revealed OT's anti-nociceptive effect, protective effect over gut injury, potential of using microbiota to naturally increase endogenous levels, which shed light on management disorders with lower side effects. However, no current comprehensive review available actions tract. This aims present lesser-known tract, recent findings are discussed regarding distribution functional OTR signalling regulating (patho)physiological functions Special emphasis placed therapeutic disorders, pain, disease (IBD), irritable syndrome (IBS). characterisation OTR's crystal structure advanced research designing identifying new OTR-specific molecules. Future in-depth basic needed further elucidate involvement detailed mechanism development ligands.

Язык: Английский

Процитировано

0