Vatier J, Bessac J F, Bonfils S
Arzneimittelforschung. 1983;33(11):1573-6.
The inhibitory effect on gastric secretion of a phenothiazine molecule, N,N-dimethyl-10-(3-quinuclidinyl)-2-phenothiazine sulfonamide (LM 24056), was studied in dogs equipped with gastric fistula (GF) and Heidenhain denervated pouch (HP). LM 24056 was infused intravenously before exogenous stimulations started: the gastric stimulation ws obtained either by gastrin, by combination of gastrin + bethanechol (subthreshold dose) or by histamine. 1. On gastrin-stimulated secretion, preliminary infusion of LM 24056 results in a weak and non-significant reduction on GF acid secretion, while on HP, the inhibition is significant with 1 and 2 micrograms x kg-1 x h-1 of gastrin. The LM 24056 concentrations which produced 50% inhibition (IC50) of acid secretion is close to 0.5 mg x min-1. 2. LM 24056 exerts a strong inhibitory effect on combination gastrin + bethanechol-stimulated acid and pepsin secretions on GH and HP. IC50 is close to 0.25 mg x min-1. 3. LM 24056 is able to delay the histamine-stimulated acid secretion. There are some differences in the gastric inhibitory effects in relation to the moment of LM 24056 administration regarding exogenous stimulant: LM 24056 seems to be able to compete gastrin and to delay the normal histamine stimulation. The most important inhibitory effect is exerted on combination gastrin + bethanechol. LM 24056 could act as an antigastrinic substance.
在配备胃瘘(GF)和海登海因去神经小胃(HP)的犬中,研究了一种吩噻嗪分子N,N - 二甲基 - 10 - (3 - 喹核烷基) - 2 - 吩噻嗪磺酰胺(LM 24056)对胃分泌的抑制作用。在开始外源性刺激之前静脉输注LM 24056:胃刺激通过胃泌素、胃泌素 + 氨甲酰甲胆碱(阈下剂量)组合或组胺来实现。1. 对于胃泌素刺激的分泌,预先输注LM 24056导致GF胃酸分泌有微弱且无统计学意义的减少,而在HP中,当胃泌素剂量为1和2微克·千克⁻¹·小时⁻¹时,抑制作用显著。产生50%酸分泌抑制(IC50)的LM 24056浓度接近0.5毫克·分钟⁻¹。2. LM 24056对胃泌素 + 氨甲酰甲胆碱刺激的GH和HP中的胃酸和胃蛋白酶分泌具有强烈的抑制作用。IC50接近0.25毫克·分钟⁻¹。3. LM 24056能够延迟组胺刺激的胃酸分泌。关于外源性刺激物,LM 24056给药时刻的胃抑制作用存在一些差异:LM 24056似乎能够竞争胃泌素并延迟正常的组胺刺激。最重要的抑制作用是对胃泌素 + 氨甲酰甲胆碱组合的作用。LM 24056可能作为一种抗胃泌素物质起作用。