Planta Med 2004; 70(4): 328-333
DOI: 10.1055/s-2004-818944
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Cardiovascular Effects Induced by Reticuline in Normotensive Rats

Katy Lísias Gondim Dias1 , Celidarque da Silva Dias1 , José Maria Barbosa-Filho1 , Reinaldo Nóbrega Almeida1 , Nadja de Azevedo Correia2 , Isac Almeida Medeiros1
  • 1Laboratório de Tecnologia Farmacêutica, Universidade Federal da Paraíba, João Pessoa-PB, Brazil
  • 2Departamento de Fisiologia e Patologia, Universidade Federal da Paraíba, João Pessoa-PB, Brazil
Further Information

Publication History

Received: August 5, 2003

Accepted: January 25, 2004

Publication Date:
19 April 2004 (online)

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Abstract

The cardiovascular effects of reticuline, isolated in a pure form from the stem of Ocotea duckei Vattimo, were studied in rats by using a combined in vivo and in vitro approach. In normotensive rats, reticuline (5, 10 and 20 mg/kg, i. v., randomly) injections produced an intense hypotension. This hypotensive response was attenuated after either, L-NAME (20 mg/kg, i. v.), a nitric oxide (NO) synthase inhibitor, or atropine (2 mg/kg, i. v.), a muscarinic receptor antagonist. In isolated rat aortic rings with intact endothelium, reticuline (3 × 10 - 6, 3 × 10 - 5, 3 × 10 - 4, 9 × 10 - 4 and 1.5 × 10 - 3 M) inhibited in a concentration-dependent manner the contractions induced by phenylephrine (1 μM), KCl (80 mM) and KCl (30 mM), [IC50 = (0.4 ± 0.1, 2.4 ± 0.4 and 3 ± 0.4) × 10 - 4 M, respectively). The effect of reticuline on phenylephrine-induced contractions was attenuated by removal of the vascular endothelium [IC50 = (2.5 ± 0.7) × 10 - 4 M]. Similar results were obtained after pretreatment of the rings with L-NAME 100 μM [IC50 = (1.3 ± 0.1) × 10 - 4 M], L-NAME 300 μM [IC50 = (3 ± 0.3) × 10 - 4 M] or atropine 1 μM [IC50 = (1.2 ± 0.2) × 10 - 4 M]. On the other hand, the effect of reticuline on phenylephrine-induced contractions was not affected by indomethacin 1 μM [IC50 = (0.7 ± 0.3) × 10 - 4 M]. Reticuline (3 × 10 - 6, 3 × 10 - 5, 3 × 10 - 4, 9 × 10 - 4 and 1.5 × 10 - 3 M) antagonized CaCl2-induced contractions, and also inhibited the intracellular calcium dependent transient contractions induced by norepinephrine (1 μM), but not those induced by caffeine (20 mM). These results suggest that the hypotensive effect of reticuline is probably due to a peripheral vasodilation in consequence of: 1) muscarinic stimulation and NOS activation in the vascular endothelium, 2) voltage-dependent Ca2+ channel blockade and/or 3) inhibition of Ca2+ release from norepinephrine-sensitive intracellular stores.

References

Prof. Isac Almeida Medeiros

Laboratório de Tecnologia Farmacêutica

Universidade Federal da Paraíba

Caixa Postal 5009

58051-970 João Pessoa, PB

Brazil

Fax: +55-832167511 or 832167365

Email: isacmed@uol.com.br