Clinical Overview

Oxytocin is a cyclic nonapeptide neurohormone synthesized in the hypothalamic paraventricular and supraoptic nuclei and released from posterior pituitary terminals. In research contexts, Oxytocin 2 mg formulations are employed to study neuroendocrine modulation, social cognition, and smooth-muscle contractility through precise peptide receptor signaling.

Mechanism of Action

Target: Oxytocin receptor (OXTR), a G-protein–coupled receptor (GPCR) distributed in uterine, mammary, and central neural tissues.
Mode: Ligand binding activates phospholipase C → IP₃/DAG cascade → intracellular Ca²⁺ release, stimulating smooth-muscle contraction and modulating neuronal firing patterns in limbic and brain-stem circuits.
Central Activity: OXTR expression within amygdala, nucleus accumbens, and prefrontal cortex underlies ongoing research into empathy, bonding, stress regulation, and autonomic control.

Research Applications

Behavioral neuroscience and social-affiliation studies • Stress-axis modulation (HPA feedback) • Smooth-muscle physiology and uterotonic assays • Lactation and endocrine-release models • Cardiovascular and autonomic research involving oxytocinergic pathways.

Purity & Quality Assurance

Revitalized Health peptides are manufactured under cGMP-aligned conditions with pharmaceutical-grade reagents. Each Oxytocin 2 mg lot is confirmed at ≥99 % purity by HPLC and structurally verified via LC-MS/MS. Lots are evaluated for appearance, solubility, and microbial/endotoxin compliance to research-grade standards. Batch-specific Certificates of Analysis document analytical data and traceability.

Storage & Stability

Store lyophilized vials at 2–8 °C, protected from light and moisture. Following reconstitution with bacteriostatic water, maintain at 2–8 °C and utilize within 20 days. Avoid repeated freeze–thaw cycles to preserve conformational integrity and receptor-binding fidelity.

Research Disclaimer

For laboratory research use only. Not intended for human consumption, therapeutic, or diagnostic application. Supplied exclusively to qualified professionals conducting controlled scientific investigations.

Formulated for research applications. Purity, identity, and lot analytics available per batch. Not medical advice.

Mechanism Strength
93/100
OXTR (Gq/PLC/IP₃–Ca²⁺) GPCR signaling
Neuroendocrine Impact
82/100
Amygdala/salience mod. • social cognition
Evidence Level
88/100
Robust mechanistic • mixed human endpoints
Safety & Tolerability
80/100
Nasal irritation/headache; uterotonic cautions
PK / PD
Plasma t½ (IV)
Onset (Intranasal)
OXTR Selectivity vs. AVPR
Functional CNS Engagement
Mechanism & Testing

Identity: Oxytocin, a cyclic nonapeptide (Cys–Tyr–Ile–Gln–Asn–Cys–Pro–Leu–Gly-NH2) with intramolecular disulfide bridge; endogenous hypothalamic neurohormone.
Mode: Binds the oxytocin receptor (OXTR), a Gq/11-coupled GPCR → PLCβ activation → IP3/DAG → Ca²⁺ mobilization and downstream kinase cascades. Peripheral: uterotonic effects on myometrium and milk ejection via myoepithelial contraction. CNS (research): modulatory effects on amygdala reactivity, social salience, trust/affiliation paradigms, and stress-axis signaling; outcomes vary by dose, timing, sex, and context.
Analytics: Identity/purity by HPLC/LC-MS; peptide content & counter-ion profile; sterility/endotoxin where applicable; stability (accelerated/real-time). PD readouts (research): eye-tracking and emotion recognition tasks, RMET/Trust tasks, fMRI (amygdala/insula connectivity), HRV/cortisol, nasal tolerability scales. Cautions: avoid pregnancy/lactation use without clinical supervision due to uterotonic and lactation effects; large parenteral doses historically linked to fluid retention/hyponatremia risk—dose/formulation discipline required.

Educational, research-style overview of a neuroendocrine peptide. Not medical advice or a treatment claim.