磺胺甲恶唑对小鼠胰腺β细胞KATP通道的抑制作用。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2023-09-28 eCollection Date: 2023-07-01 DOI:10.1177/15593258231203611
Hiroshi Ogata, Shigeki Kitamura, Makoto Fujiwara, Masaru Shimizu, Chengbo Tan, Songji Zhao, Yuko Maejima, Kenju Shimomura
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引用次数: 0

摘要

磺胺甲恶唑(SMX)作为一种临床应用广泛的抗生素,有低血糖副作用。这是因为SMX含有磺酰胺结构,它关闭ATP敏感性钾(KATP)通道并诱导胰岛素分泌。然而,目前还没有详细的报告来测量可以关闭KATP通道并诱导胰岛素分泌的有效剂量。在本研究中,利用全细胞膜片钳记录来测量SMX对胰腺β细胞KATP通道活性的影响。此外,对小鼠胰岛的静态孵育试验进行评估,以测量SMX的胰岛素分泌能力。SMX在较高浓度下可抑制胰腺β细胞膜KATP通道并诱导胰岛素分泌。SMX对KATP通道活性的半最大抑制浓度(IC50)为.46±0.08mM。还表明,当同时应用低浓度磺酰脲时,接近IC50浓度的SMX(.5mM)能够几乎完全阻断KATP通道,甲苯丁酰胺(.01mM)。我们目前的数据为临床使用SMX治疗磺脲类药物治疗糖尿病患者感染提供了重要信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dose Dependent Effect of Sulfamethoxazole on Inhibiting K<sub>ATP</sub> Channel of Mouse Pancreatic β Cell.

Dose Dependent Effect of Sulfamethoxazole on Inhibiting K<sub>ATP</sub> Channel of Mouse Pancreatic β Cell.

Dose Dependent Effect of Sulfamethoxazole on Inhibiting K<sub>ATP</sub> Channel of Mouse Pancreatic β Cell.

Dose Dependent Effect of Sulfamethoxazole on Inhibiting KATP Channel of Mouse Pancreatic β Cell.

Sulfamethoxazole (SMX) is widely used as an antibiotic in the clinical application with side effects of hypoglycemia. This is because SMX contains the sulfonamide structure, which closes ATP-sensitive potassium (KATP) channels and induces insulin secretion. However, there are no detail reports that measure the effective dose that can close KATP channels and induce insulin secretion. In this study, whole-cell patch clamp recording was utilized to measure the effect of SMX on KATP channel activity on pancreatic β cells. Also, the static incubation assay with mice islets was assessed to measure the insulin secretion capacity of SMX. SMX was shown to inhibit the KATP channel in pancreatic β cell membrane and induce insulin secretion in relatively high concentration. The half maximal inhibitory concentration (IC50) for KATP channel activity of SMX was .46 ± .08 mM. It was also shown that a near IC50 concentration of SMX (.5 mM) was able to nearly fully block the KATP channel when simultaneously applied with low concentration sulfonylurea, tolbutamide (.01 mM). Our present data provide important information for the clinical use of SMX to treat infection in diabetic patients using sulfonylureas.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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