Related Experiment Video
Updated: May 1, 2026

Assessment of Morphine-induced Hyperalgesia and Analgesic Tolerance in Mice Using Thermal and Mechanical Nociceptive Modalities
Published on: July 29, 2014
Treatment with steroid hormones and morphine alters general activity, sexual behavior, and opioid gene expression in
E Teodorov1, R Camarini2, M M Bernardi1
1Centro de Matemática, Computação e Cognição, Universidade Federal do ABC, Av dos Estados, 5001, Brazil.
Aims:
Previous studies have shown that brain opioid peptides exert an inhibitory influence on gonadotropin secretion. Different types of brain opioids, such as β-endorphin, enkephalin, and dynorphin, exert their actions by binding to specific opioid receptors (i.e., μ, δ, and κ, respectively). The present study determined the effects of chronic treatment with morphine in female rats with pharmacologically induced estrus on behavior and opioid receptor gene and protein expression in the hypothalamus, striatum, and periaqueductal gray.
Main Methods:
Female ovariectomized rats treated with estrogen+progesterone received 3.5mg/kg morphine once per day for 6days. We evaluated general activity, sexual behavior, Oprm1, Oprd1, and Oprk1 gene expression, and μ opioid receptor (MOR), δ opioid receptor (DOR), and κ opioid receptor (KOR) protein expression in the hypothalamus, striatum, and periaqueductal gray in adult virgin female ovariectomized rats.
Key Findings:
Chronic morphine treatment increased locomotion and grooming behavior, decreased immobility time, decreased sexual behavior, and decreased the lordosis quotient. The molecular biology results showed that morphine treatment increased Oprm1 gene and MOR protein expression in the striatum and decreased KOR protein expression in the hypothalamus in animals that were assessed for general activity. The animals that were evaluated for sexual behavior exhibited an increase in Oprm1 expression in the periaqueductal gray and increase in KOR expression in the striatum.
Significance:
These results suggest that both opioid system activation and sex hormones alter behavioral and molecular patterns in ovariectomized rats within a relatively short period of time.
Insights
Chronic morphine alters rat behavior and opioid receptor expression, indicating opioid system activation and sex hormones impact these patterns quickly. Keywords: morphine, opioid receptors, behavior, sex hormones, rats.
Area of Science:
- Neuroscience
- Endocrinology
- Pharmacology
Background:
- Brain opioid peptides inhibit gonadotropin secretion.
- Opioid peptides (β-endorphin, enkephalin, dynorphin) act via specific receptors (μ, δ, κ).
Purpose of the Study:
- To investigate the effects of chronic morphine on behavior and opioid receptor expression.
- To examine changes in hypothalamus, striatum, and periaqueductal gray in female rats with induced estrus.
Main Methods:
- Ovariectomized female rats received daily morphine for 6 days.
- Evaluated general activity, sexual behavior, and opioid receptor (Oprm1, Oprd1, Oprk1) gene and protein expression.
Main Results:
- Morphine increased locomotion/grooming, decreased immobility and sexual behavior.
- Increased μ opioid receptor (MOR) gene/protein in striatum; decreased κ opioid receptor (KOR) protein in hypothalamus.
- Increased MOR gene in periaqueductal gray and KOR gene in striatum in sexually behavior-tested animals.
Conclusions:
- Opioid system activation and sex hormones rapidly alter behavioral and molecular patterns.
- Suggests a short-term interplay between opioids, hormones, and neural pathways.
Related Concept Videos
Opioid Analgesics: Morphine and Other Natural Cogeners
Opioid Receptors: Overview
Analgesia and Pain Management
Opioid Analgesics: Synthetic and Semisynthetic Opioids

