Related Experiment Videos
[Vasoactive intestinal polypeptide induced prolactin release is model dependent in free-moving rats]
B C Zhu1, J H Han, S R Chiocchio
1Department of Biology, East China Normal University, Shanghai 200062.
Sheng Li Xue Bao : [Acta Physiologica Sinica]
|August 14, 2001
Summary
Vasoactive intestinal polypeptide (VIP) stimulates prolactin (PRL) release in vivo, but its effect varies significantly based on the animal's physiological state, including sex and reproductive status.
Area of Science:
- Endocrinology
- Neuroendocrinology
- Physiology
Background:
- In vitro studies indicated that vasoactive intestinal polypeptide (VIP) stimulates pituitary prolactin (PRL) release, contingent on the animal's endocrine status.
- The in vivo effects of VIP on PRL secretion under varying physiological conditions remained largely undetermined.
Purpose of the Study:
- To investigate the in vivo effects of VIP on PRL secretion in rats.
- To determine if VIP's PRL-releasing activity is modulated by different physiological states, such as sex and lactation.
Main Methods:
- Rats were infused with VIP (5 µg/100 g body weight) via jugular vein cannulation.
- Blood samples were collected at intervals to measure VIP and PRL concentrations.
- Different physiological states were examined, including male, female (diestrus, proestrus), and lactating (suckled, separated) rats.
Main Results:
- VIP infusion rapidly increased VIP blood concentrations, peaking at 10 minutes and sustained for over 30 minutes.
- VIP significantly increased PRL concentrations in all tested animals (P < 0.05).
- The PRL response to VIP was highest in males and significantly lower in females and lactating rats, with notable differences between suckled and separated lactating mothers.
Conclusions:
- VIP administration in vivo stimulates PRL release.
- The magnitude of VIP-induced PRL secretion is significantly influenced by the animal's endocrine and neural status, including sex and reproductive condition.
- These findings highlight the context-dependent action of VIP in regulating prolactin secretion in vivo.