Receptor-mediated biological effects of extracts obtained from three Asplenium species

Author:

Petkov Venelin H.1ORCID,Ardasheva Raina G.2ORCID,Prissadova Natalia A.2ORCID,Kristev Athanas D.2,Stoyanov Plamen S.13ORCID,Argirova Mariana D.4ORCID

Affiliation:

1. Department of Botany and Methods of Biology Teaching, Faculty of Biology , University of Plovdiv “Paisii Hilendarski” , 24 Tzar Assen Str. , 4000 Plovdiv , Bulgaria

2. Department of Medical Physics and Biophysics, Faculty of Pharmacy , Medical University of Plovdiv , 15A Vassil Aprilov Str. , 4002 Plovdiv , Bulgaria

3. Department of Bioorganic Chemistry , Faculty of Pharmacy, Medical University of Plovdiv , 15A Vassil Aprilov Str., 4002 Plovdiv , Bulgaria

4. Department of Chemical Sciences, Faculty of Pharmacy , Medical University of Plovdiv , 15A Vassil Aprilov Str. , 4002 Plovdiv , Bulgaria

Abstract

Abstract This study reports the effects of aqueous extracts obtained from three fern species of Bulgarian origin: Asplenium ceterach L., Asplenium scolopendrium L., and Asplenium trichomanes L. on the contractility and bioelectrogenesis of rat gastric smooth muscle tissues. In the concentration range 0.015–0.150 mg/mL the three extracts contracted smooth muscle tissues in a concentration-dependent manner. The contractions caused by A. ceterach L. and A. scolopendrium L. extracts (0.150 mg/mL) were reduced by ketanserin (5 × 10−7 and 5 × 10−6 mol/L), an antagonist of serotonin 5-HT2 receptor. The contraction evoked by A. trichomanes L. (0.150 mg/mL) was significantly reduced by 1 × 10−6 mol/L atropine, an antagonist of muscarinic receptors, and turned into relaxation against the background of 3 × 10−7 mol/L galantamine. After combined pretreatment with galantamine and l-arginine (5 × 10−4 mol/L), this relaxation become more pronounced. The study demonstrates that constituents of A. ceterach L. and A. scolopendrium L. extracts act as agonists of 5-HT2 receptors and cause contraction by activating serotonergic signaling system. A. trichomanes L.-induced reaction is an additive result of two opposite-in-character effects. The dominant contraction is initiated by inhibition of acetylcholinesterase activity. The relaxation develops with pre-inhibited acetylcholinesterase, it is significantly potentiated by l-arginine, and therefore associated with nitrergic signaling pathway.

Publisher

Walter de Gruyter GmbH

Subject

General Biochemistry, Genetics and Molecular Biology

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