Planta Med 2003; 69(12): 1080-1085
DOI: 10.1055/s-2003-45186
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Antispasmodic Effect of the Essential Oil of Plectranthus barbatus and some Major Constituents on the Guinea-Pig Ileum

Carlos C. Câmara1 , Nilberto R. F. Nascimento2 , 3 , Carlos L. Macêdo-Filho2 , Fábio B. S. Almeida2 , Manassés C. Fonteles2 , 3
  • 1Escola Superior de Agricultura de Mossoró, Departamento de Veterinária, Mossoró, Rio Grande do Norte, Brasil
  • 2Unidade de Pesquisas Clínicas, Faculdade de Medicina, Universidade Federal do Ceará (UFC), Porangabussú, Fortaleza, Ceará, Brasil
  • 3Faculdade de Veterinária, Universidade Estadual do Ceará (UECE), Campus do Itaperi, Fortaleza, Ceará, Brasil
Further Information

Publication History

Received: April 22, 2003

Accepted: October 18, 2003

Publication Date:
29 January 2004 (online)

Abstract

The effects of the Plectranthus barbatus essential oil (PBEO) at concentrations ranging form 1 to 300 μg/mL and some major constituents, i. e., α-pinene, myrcene and caryophyllene in the ratio and amount found in the oil, were studied on the contractility of the guinea-pig ileum. PBEO decreased the basal tonus of the ileum with a maximal response (Rmax; % of K+-contraction) of 62.7 ± 3.8 % compared with 36.6 ± 4.5 % inhibition achieved with α-pinene and 68 ± 2.6 % with papaverine. The other constituents had only a slight effect. PBEO also blocked the phasic contractions evoked by acetylcholine with an Rmax of 85 ± 3.6 % compared with 54.4 ± 3.5 % inhibition induced by α-pinene and 12.4 ± 5.6 % with caryophyllene. The contractions induced by histamine or barium chloride were also decreased in amplitude by PBEO with an Rmax of 94.3 ± 5.7 % and 100 %, respectively. In addition, PBEO relaxed tissues pre-contracted with 60 mM K+ with an Rmax of 89.7 ± 2.7 % compared with 55.4 ± 4.6 % relaxation induced by α-pinene. The other major constituents studied had no significant effect. Furthermore, at the higher concentration used, i. e., 300 μg/mL, PBEO decreased the maximal response of calcium chloride (10 - 7 to 10 - 3 M) induced contraction in depolarized tissues by 29.1 ± 9.53 % (p < 0.05). In addition, the component of the contraction elicited by a single dose of carbachol (CCh; 100 μM) added on nifedipine (10 μM) treated tissues or at very low extracellular calcium concentration were blocked by PBEO (300 μg/mL) in 85.7 ± 7.8 % (p < 0.05; n = 5) and 81.2 ± 6.4 % (p < 0.05; n = 4), respectively. These data show that PBEO has intestinal relaxant and antispasmodic activity and suggest that this effect is not related to antagonism in extracellular receptors for neurotransmitters or autacoids and it seems to occur downstream of calcium entry or release from internal stores. The main active principle for its relaxant and spasmolytic activity seems to be α-pinene.

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Manassés C. Fonteles, M.D., Ph.D

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