Laboratory of Pharmacology and Immunity, Institute of Biological Sciences and Health, Federal University of Alagoas, Maceió 57020-720, AL, Brazil.
Mar Drugs. 2013 May 13;11(5):1553-64. doi: 10.3390/md11051553.
In this work, we investigated the spasmolytic effect of caulerpine, a bisindole alkaloid isolated from marine algae of the Caulerpa genus, on guinea pig ileum. Our findings indicated that caulerpine inhibited phasic contractions induced by carbachol (IC₅₀ = 7.0 ± 1.9 × 10⁻⁵ M), histamine (IC₅₀ = 1.3 ± 0.3 × 10⁻⁴ M) and serotonin (IC₅₀ = 8.0 ± 1.4 × 10⁻⁵ M) in a non-selective manner. Furthermore, caulerpine concentration-dependently inhibited serotonin-induced cumulative contractions (pD'₂ = 4.48 ± 0.08), shifting the curves to the right with Emax reduction and slope of 2.44 ± 0.21, suggesting a noncompetitive antagonism pseudo-irreversible. The alkaloid also relaxed the ileum pre-contracted by KCl (EC₅₀ = 9.0 ± 0.9 × 10⁻⁵ M) and carbachol (EC₅₀ = 4.6 ± 0.7 × 10⁻⁵ M) in a concentration-dependent manner. This effect was probably due to inhibition of Ca²⁺ influx through voltage-gated calcium channels (CaV), since caulerpine slightly inhibited the CaCl₂-induced contractions in depolarizing medium without Ca²⁺, shifting the curves to the right and with Emax reduction. According to these results, the spasmolytic effect of caulerpine on guinea pig ileum seems to involve inhibition of Ca²⁺ influx through CaV. However, other mechanisms are not discarded.
在这项工作中,我们研究了从 Caulerpa 属海藻中分离得到的双吲哚生物碱 caul erpine 对豚鼠回肠的松弛作用。我们的研究结果表明,caul erpine 以非选择性方式抑制 carbachol(IC₅₀=7.0±1.9×10⁻⁵M)、组胺(IC₅₀=1.3±0.3×10⁻⁴M)和 5-羟色胺(IC₅₀=8.0±1.4×10⁻⁵M)诱导的相位收缩。此外,caul erpine 浓度依赖性地抑制 5-羟色胺诱导的累积收缩(pD'₂=4.48±0.08),使曲线右移,Emax 降低,斜率为 2.44±0.21,提示非竞争性拮抗拟不可逆性。该生物碱还浓度依赖性地松弛由 KCl(EC₅₀=9.0±0.9×10⁻⁵M)和 carbachol(EC₅₀=4.6±0.7×10⁻⁵M)预收缩的回肠。这种作用可能是由于抑制通过电压门控钙通道(CaV)的 Ca²⁺内流所致,因为 caul erpine 轻微抑制去极化介质中无 Ca²⁺的 CaCl₂诱导的收缩,使曲线右移,Emax 降低。根据这些结果,caul erpine 对豚鼠回肠的松弛作用似乎涉及抑制 CaV 介导的 Ca²⁺内流。然而,其他机制并未被排除。