Planta Med 2016; 82(S 01): S1-S381
DOI: 10.1055/s-0036-1596945
Abstracts
Georg Thieme Verlag KG Stuttgart · New York

Antispasmodic and spasmolytic activity of Melissa officinalis EPS upon mice gastrointestinal tract: an ex vivo pilot study

P Aubert
1   Inserm U913-Institut des Maladies de l'Appareil Digestif du CHU de Nantes, 1 rue Gaston Veil, 44035 Nantes, France
,
I Guinobert
2   PiLeJe, 37 Quai de Grenelle, 75015 Paris, France
,
A Guilbot
2   PiLeJe, 37 Quai de Grenelle, 75015 Paris, France
,
M Dubourdeaux
3   3I Nature, Chemin des Tiolans, 03800 Saint-Bonnet de Rochefort, France
,
M Neunlist
1   Inserm U913-Institut des Maladies de l'Appareil Digestif du CHU de Nantes, 1 rue Gaston Veil, 44035 Nantes, France
› Author Affiliations
Further Information

Publication History

Publication Date:
14 December 2016 (online)

 

Introduction: Melissa officinalis is a medicinal plant widely used for its impact upon mood and cognitive performance [1] and for digestive comfort [2]. However, only a few studies [3] have characterised the impact of M. officinalis upon gastro-intestinal (GI) functions. We assessed ex vivo the antispasmodic and spasmolytic activity of M. officinalis on different segments of the GI tract of mice. Material and methods: M. officinalis was extracted using the patented process Phytostandard® that allows obtaining standardised liquid extracts from fresh plant (EPS). Segments of antrum (circular muscle; n = 10/condition) and jejunum (longitudinal muscle; n = 10/condition) of C57bl6 mice were placed in organ chambers. Isometric contractions were continuously recorded and contractile response to increasing concentrations of M. officinalis EPS (1 – 50 mg/mL) and vehicle (ethanol) were analysed. Antispasmodic activity was assessed under basal conditions. The spasmolytic effect was assessed on a steady state tissue precontracted with the muscarinergic agonist bethanechol (100µM) [4]. We measured the frequency of spontaneous phasic contractions and the area under the curve (AUC) for 2 minutes after the addition of M. officinalis EPS or vehicle [5]. Results: In the antrum, M. officinalis EPS did not modify contractile parameters under basal conditions. However, in the precontracted antrum, M. officinalis EPS at 50 mg/mL increased the AUC as compared to vehicle. In the jejunum, M. officinalis EPS decreased the frequency of spontaneous phasic contractions both under basal and precontracted conditions as compared to vehicle. Furthermore, M. officinalis EPS decreased the AUC starting at a concentration of 10 mg/mL in basal (Figure 1A) and precontracted conditions (Figure 1B) as compared to vehicle. Conclusion: Our results demonstrate that the M. officinalis EPS tested has antispasmodic and spasmolytic activity on jejunum ex vivo. The mediators involved remain to be determined.

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Keywords: Melissa officinalis, gut, antispasmodic, spasmolytic, contractility.

References:

[1] Kennedy DO, Wake G, Savelev S, Tildesley NT, Perry EK, Wesnes KA, Scholey AB. Modulation of mood and cognitive performance following acute administration of single doses of Melissa officinalis (Lemon balm) with human CNS nicotinic and muscarinic receptor-binding properties. Neuropsychopharmacol 2003; 28: 1871 – 1881

[2] Savino F, Cresi F, Castagno E, Silvestro L, Oggero R. A randomized double-blind placebo-controlled trial of a standardized extract of Matricariae recutita, Foeniculum vulgare and Melissa officinalis (ColiMil) in the treatment of breastfed colicky infants. Phytother Res. 2005; 19: 335 – 340

[3] Sadraei H, Ghannadi A, Malekshahi K. Relaxant effect of essential oil of Melissa officinalis and citral on rat ileum contractions. Fitoterapia 2003;74: 445 – 452

[4] Martín-Cano FE, Camello PJ, and Pozo MJ. Characterization of the motor inhibitory role of colonic mucosa under chemical stimulation in mice. Am J Physiol Gastrointest Liver Physiol 2014; 306: G614-G621

[5] Baudry C, Reichardt F, Marchix J, Bado A, Schemann M, des Varannes SB, Neunlist M, Moriez R. Diet-induced obesity has neuroprotective effects in murine gastric enteric nervous system: involvement of leptin and glial cell line-derived neurotrophic factor. J Physiol 2012; 590: 533 – 544