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Developmental changes in the response of rat isolated duodenum to nicotine
1Department of Pharmacology, Tokyo Women's Medical College, Japan.
European Journal of Pharmacology
|January 4, 1994
Summary
Neonatal rat duodenum contracts in response to nicotine, mediated by cholinergic pathways. Adult rat duodenum relaxes, involving complex non-adrenergic, non-cholinergic signaling with peptidergic and purinergic components.
Area of Science:
- Neurogastroenterology
- Developmental pharmacology
- Gastrointestinal physiology
Background:
- The gastrointestinal tract's response to stimuli changes significantly during development.
- Ganglionic stimulants like nicotine affect gut motility through various neural pathways.
Purpose of the Study:
- To investigate the developmental changes in the rat duodenum's response to nicotine and dimethylphenylpiperazinium.
- To elucidate the specific neurotransmitter systems involved in these responses at different life stages.
Main Methods:
- Isolated rat duodenum preparations from neonatal and adult rats.
- Recording of isotonic mechanical activity in response to ganglionic stimulants.
- Pharmacological blockade of specific neurotransmitter receptors and pathways (e.g., hexamethonium, tetrodotoxin, hyoscine, guanethidine).
Main Results:
- Neonatal duodenum exhibited contraction to nicotine/DMPP, blocked by cholinergic and neuronal inhibitors.
- Adult duodenum showed relaxation to nicotine/DMPP, blocked by neuronal inhibitors but not adrenergic/cholinergic ones.
- The shift from contraction to relaxation occurred around the third postnatal week.
- Nicotine-induced relaxation in adults involved peptidergic and purinergic (P1 and P2x purinoceptor) pathways.
Conclusions:
- The contractile response in neonatal rat duodenum is mediated by cholinergic transmission.
- The relaxant response in adult rat duodenum involves non-adrenergic, non-cholinergic (NANC) transmission, incorporating peptidergic and purinergic mechanisms.
- Significant developmental plasticity exists in the neural control of duodenal motility.