Literature DB >> 12481931

An arterially perfused decerebrate preparation of Suncus murinus (house musk shrew) for the study of emesis and swallowing.

Julia E Smith1, Julian F R Paton, Paul L R Andrews.   

Abstract

Arterially perfused, decerebrate preparations of the insectivore, Suncus murinus were made to determine whether the emetic reflex could be activated in such a preparation using a range of stimuli shown to be emetic in conscious or anaesthetised Suncus. Efferent phrenic and vagus nerve activities and electromyograms (EMGs) from the temporalis, abdominal oesophagus and trapezius muscles were recorded, as well as longitudinal shortening of the oesophagus and dorso-ventral movements of the thorax. The preparations swallowed spontaneously every 0.6 to 6.5 min. The duration of a swallow was 3.1 +/- 0.3 s (recorded as the time taken for the oesophagus to shorten and recover to its resting position) and the oesophagus shortened by 3.5 +/- 0.4 mm during a swallow. The emetic reflex was activated by electrical stimulation (30 Hz, 10-20 V, 0.2 ms pulse width, for 30 s) of abdominal vagal afferents (latency < 30 s) or by arterial perfusion with either 40 nM of the capsaicin analogue resiniferatoxin (latency 1.7 +/- 0.6 min), 6 microM nicotine (latency 1.6 +/- 0.1 min) or 1 microM of the phosphodiesterase IV inhibitor CP-80,633 (latency 8.9 +/- 3.9 min). These emetic stimuli produced somatic and visceral movements in Suncus preparations indicative of activation of the emetic reflex. There were pronounced contractions of the thorax that occurred simultaneously with oesophageal shortening and mouth opening, separated by thorax expansion and a burst of phrenic nerve activity. During emetic-like episodes, oesophageal shortenings were only 0.84 +/- 0.1 s in duration, faster than the duration of shortening observed during swallowing (cf. swallowing, 3.1 +/- 0.3 s; P < 0.0001). The shortening of the oesophagus during emetic-like episodes was 6.2 +/- 0.4 mm, which was greater than the shortening seen during swallowing (cf. swallowing, 3.5 +/- 0.4 mm; P < 0.0001). We conclude that the emetic reflex can be activated in our Suncus preparations and that this non-sentient small adult animal model can now be used to study the neurophysiology and pharmacology of swallowing and emesis.

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Year:  2002        PMID: 12481931     DOI: 10.1113/eph8702424

Source DB:  PubMed          Journal:  Exp Physiol        ISSN: 0958-0670            Impact factor:   2.969


  14 in total

1.  Role of the abdominal vagus and hindbrain in inhalational anesthesia-induced vomiting.

Authors:  Ragini G Gupta; Claire Schafer; Yolande Ramaroson; Michael G Sciullo; Charles C Horn
Journal:  Auton Neurosci       Date:  2016-07-02       Impact factor: 3.145

2.  Ponto-medullary nuclei involved in the generation of sequential pharyngeal swallowing and concomitant protective laryngeal adduction in situ.

Authors:  Tara G Bautista; Mathias Dutschmann
Journal:  J Physiol       Date:  2014-03-17       Impact factor: 5.182

3.  Post-anesthesia vomiting: impact of isoflurane and morphine on ferrets and musk shrews.

Authors:  Charles C Horn; Kelly Meyers; Diana Pak; Allysa Nagy; Christian C Apfel; Brian A Williams
Journal:  Physiol Behav       Date:  2012-04-04

4.  Computerized detection and analysis of cancer chemotherapy-induced emesis in a small animal model, musk shrew.

Authors:  Dong Huang; Kelly Meyers; Séverine Henry; Fernando De la Torre; Charles C Horn
Journal:  J Neurosci Methods       Date:  2011-03-15       Impact factor: 2.390

Review 5.  Why is the neurobiology of nausea and vomiting so important?

Authors:  Charles C Horn
Journal:  Appetite       Date:  2007-10-11       Impact factor: 3.868

6.  Chemotherapy-induced kaolin intake is increased by lesion of the lateral parabrachial nucleus of the rat.

Authors:  Charles C Horn; Bart C De Jonghe; Kathleen Matyas; Ralph Norgren
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-08-26       Impact factor: 3.619

Review 7.  Opportunities for the replacement of animals in the study of nausea and vomiting.

Authors:  A M Holmes; J A Rudd; F D Tattersall; Q Aziz; P L R Andrews
Journal:  Br J Pharmacol       Date:  2009-04-09       Impact factor: 8.739

8.  Chemotherapy agent cisplatin induces 48-h Fos expression in the brain of a vomiting species, the house musk shrew (Suncus murinus).

Authors:  Bart C De Jonghe; Charles C Horn
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2009-02-18       Impact factor: 3.619

Review 9.  Pathophysiological and neurochemical mechanisms of postoperative nausea and vomiting.

Authors:  Charles C Horn; William J Wallisch; Gregg E Homanics; John P Williams
Journal:  Eur J Pharmacol       Date:  2013-10-26       Impact factor: 4.432

10.  Impact of electrical stimulation of the stomach on gastric distension-induced emesis in the musk shrew.

Authors:  C C Horn; L Zirpel; M G Sciullo; D M Rosenberg
Journal:  Neurogastroenterol Motil       Date:  2016-04-12       Impact factor: 3.598

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