» Articles » PMID: 7658369

Characteristic Features of Inhibitory Junction Potentials Evoked by Single Stimuli in the Guinea-pig Isolated Taenia Caeci

Overview
Journal J Physiol
Specialty Physiology
Date 1995 May 15
PMID 7658369
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

1. Changes in membrane potential of the guinea-pig isolated taenia caeci evoked by single stimuli have been investigated using intracellular recording techniques. Nifedipine (10 microM) was used to arrest spontaneous muscle action potentials. Single stimuli elicited complex junction potentials which consisted of both excitatory and inhibitory components. 2. The excitatory component of the compound junction potential was unaffected by hexamethonium (100 microM) but abolished by atropine (1 microM) and omega-conotoxin GVIA (10-100 nM). 3. In the presence of atropine, single stimuli elicited fast inhibitory junction potentials (IJPs). IJPs were sometimes biphasic during repolarization with a noticeable 'slow tail'. Apamin (30-100 nM) potently inhibited the fast IJP and revealed an underlying slow IJP. 4. The fast IJP was also abolished by omega-conotoxin GVIA (100 nM). However, the slow IJP was insensitive to omega-conotoxin GVIA but was abolished by cadmium (30 microM). 5. Guanethidine (3 microM) and N omega-nitro-L-arginine (10-100 microM) had no detectable effects on either of the IJPs. The dye Reactive Blue 2 reduced the amplitude of the fast IJP but this reduction was associated with a membrane hyperpolarization. 6. The existence of two distinct IJPs in the guinea-pig taenia caeci has been demonstrated. The ability of omega-conotoxin GVIA to selectively abolish the fast IJP leaving the slow IJP intact suggests that separate nerves are involved in mediating these responses.

Citing Articles

Neurotransmitters responsible for purinergic motor neurotransmission and regulation of GI motility.

Sanders K, Mutafova-Yambolieva V Auton Neurosci. 2021; 234:102829.

PMID: 34146957 PMC: 8575072. DOI: 10.1016/j.autneu.2021.102829.


Burnstock and the legacy of the inhibitory junction potential and P2Y1 receptors.

King B Purinergic Signal. 2020; 17(1):25-31.

PMID: 33125617 PMC: 7954919. DOI: 10.1007/s11302-020-09747-6.


Optogenetic analysis of neuromuscular transmission in the colon of ChAT-ChR2-YFP BAC transgenic mice.

Perez-Medina A, Galligan J Am J Physiol Gastrointest Liver Physiol. 2019; 317(5):G569-G579.

PMID: 31411893 PMC: 6879885. DOI: 10.1152/ajpgi.00089.2019.


The purinergic neurotransmitter revisited: a single substance or multiple players?.

Mutafova-Yambolieva V, Durnin L Pharmacol Ther. 2014; 144(2):162-91.

PMID: 24887688 PMC: 4185222. DOI: 10.1016/j.pharmthera.2014.05.012.


Differential release of β-NAD(+) and ATP upon activation of enteric motor neurons in primate and murine colons.

Durnin L, Sanders K, Mutafova-Yambolieva V Neurogastroenterol Motil. 2013; 25(3):e194-204.

PMID: 23279315 PMC: 3578016. DOI: 10.1111/nmo.12069.


References
1.
Costa M, Furness J, Humphreys C . Apamin distinguishes two types of relaxation mediated by enteric nerves in the guinea-pig gastrointestinal tract. Naunyn Schmiedebergs Arch Pharmacol. 1986; 332(1):79-88. DOI: 10.1007/BF00633202. View

2.
Maas A . The effects of apamin on responses evoked by field stimulation in guinea-pig taenia caeci. Eur J Pharmacol. 1981; 73(1):1-9. DOI: 10.1016/0014-2999(81)90139-4. View

3.
Iselin C, Martin J, Magistretti P, Ferrero J . Stimulation by nicotine of enteric inhibitory nerves and release of vasoactive intestinal peptide in the taenia of the guinea-pig caecum. Eur J Pharmacol. 1988; 148(2):179-86. DOI: 10.1016/0014-2999(88)90562-6. View

4.
Shikano K, Long C, Ohlstein E, Berkowitz B . Comparative pharmacology of endothelium-derived relaxing factor and nitric oxide. J Pharmacol Exp Ther. 1988; 247(3):873-81. View

5.
Den Hertog A, van den Akker J, Nelemans A . Suramin and the inhibitory junction potential in taenia caeci of the guinea-pig. Eur J Pharmacol. 1989; 173(2-3):207-9. DOI: 10.1016/0014-2999(89)90522-0. View