Standard Dosage Range
Research dosing range: No standardized human dosage. Preclinical: 0.1-1 mg/kg
Educational reference only
Dosage by Use Case
Antipsychotic Effects (Research)
2-8 weeks
Animal studies. Subcutaneous or intraperitoneal. Targets NTS1 receptors. Consider potential hypothermia.
Analgesia (Research)
1-4 weeks
Animal studies. Intrathecal or subcutaneous. Targets NTS2 receptors. Limited human data.
Metabolic Regulation (Research)
4-12 weeks
Animal studies. Subcutaneous. Investigating effects on fat metabolism. Monitor for potential GI side effects.
Neuroprotection (Research)
2-6 weeks
Animal studies. Investigating hypothermic neuroprotection. Consider route of administration to target CNS.
Timing & Frequency
Timing depends on the target application. For CNS effects, intranasal administration may provide faster onset. Subcutaneous injections can be timed based on half-life and desired effect duration.
Cycle Guidance
Due to limited human data, cycle guidance is largely based on preclinical studies. Shorter cycles (2-8 weeks) with breaks are commonly used. Monitor for any adverse effects and adjust accordingly.
Reconstitution Reference
Quick reference for reconstituting Neurotensin. For custom vial sizes and concentrations, use the Reconstitution Calculator.
| Common Vial Size | Varies |
| BAC Water Volume | Refer to manufacturer instructions for desired concentration |
| Concentration & Draw | Varies depending on experimental design and target dosage |
| Storage | Refrigerate after reconstitution. Follow manufacturer instructions. |
| Stability | Consult manufacturer specifications for reconstituted solution stability. |
Frequently Asked Questions
What is the typical dosage of neurotensin for antipsychotic research?
How is neurotensin typically administered?
What are the potential side effects of neurotensin administration?
Last updated: 2026-02-19