Pereira Joedna Cavalcante, Figueiredo Indyra Alencar Duarte, de Oliveira Filipe Rodolfo Moreira Borges, Ferreira Sarah Rebeca Dantas, Aires Moreno Giulyane Targino, da Silva Tania Maria Sarmento, Pinheiro Ulisses Dos Santos, Santos Barbara Viviana de Oliveira, da Silva Bagnólia Araújo, Cavalcante Fabiana de Andrade
Programa de Pós-graduação em Produtos Naturais e Sintéticos Bioativos, Universidade Federal da Paraíba, João Pessoa, Brazil.
Curso de Farmácia, Universidade Federal da Paraíba, João Pessoa, Brazil.
Front Pharmacol. 2020 Dec 23;11:572574. doi: 10.3389/fphar.2020.572574. eCollection 2020.
Santos-Neto, Nascimento, Cavalcanti and Pinheiro sponges are distributed across tropical worldwide seas. Some studies of marine products have shown interesting activities in smooth muscle models. Hence, we assessed the effect of the ethanolic extract of . (OC-EtOH) on acute toxicity and gastrointestinal motility ( and ) in rodent models. On guinea pig ileum, OC-EtOH induced a concentration dependent contraction on basal tonus, which was not inhibited by atropine, but in the presence of pyrilamine or verapamil, the effect was antagonized. Contrastingly, on KCl- or histamine-induced contractions, OC-EtOH presented a transient contraction followed by a concentration-dependent relaxation. Moreover, OC-EtOH presented a relaxant profile on cumulative curves to CaCl and tonic contraction induced by S-(-)-BayK8644, through Cav blockade. The acute toxicity assay showed that OC-EtOH (2,000 mg/kg, p.o.) did not present any sign of toxicity in female mice. Additionally, OC-EtOH presented antidiarrheal effect in mice, increased the intestinal normal transit and reduced the castor oil-induced intestinal transit. Thus, OC-EtOH presented a dual effect on guinea pig ileum promoting contraction through activation of H and Ca, and relaxation through Ca blockade, besides the effect on upper gastrointestinal transit in mice, showing a potential medicinal use of this sponge in intestinal diseases such as diarrhea.
桑托斯 - 内托、纳西门托、卡瓦尔坎蒂和皮涅罗海绵分布于全球热带海域。一些海产品研究表明其在平滑肌模型中具有有趣的活性。因此,我们评估了[具体名称]乙醇提取物(OC - EtOH)对啮齿动物模型急性毒性和胃肠动力([具体指标1]和[具体指标2])的影响。在豚鼠回肠上,OC - EtOH对基础张力诱导浓度依赖性收缩,该收缩不受阿托品抑制,但在存在吡苄明或维拉帕米时,该作用被拮抗。相反,在氯化钾或组胺诱导的收缩中,OC - EtOH呈现短暂收缩,随后是浓度依赖性舒张。此外,通过钙通道阻滞,OC - EtOH在累积氯化钙曲线和S - (-)-BayK8644诱导的强直性收缩上呈现舒张曲线。急性毒性试验表明,OC - EtOH(2000毫克/千克,口服)在雌性小鼠中未表现出任何毒性迹象。此外,OC - EtOH在小鼠中呈现止泻作用,增加肠道正常转运并减少蓖麻油诱导的肠道转运。因此,OC - EtOH对豚鼠回肠呈现双重作用,通过激活H和Ca促进收缩,并通过钙通道阻滞舒张,此外对小鼠上消化道转运也有作用,显示出这种海绵在腹泻等肠道疾病中的潜在药用价值。