Department of Pharmacological Screening, Jagiellonian University Medical College, Medyczna 9, 30-688 Cracow, Poland.
Department of Pharmacokinetics and Physical Pharmacy, Jagiellonian University Medical College, Medyczna 9, 30-688 Cracow, Poland.
Int J Mol Sci. 2023 Apr 19;24(8):7499. doi: 10.3390/ijms24087499.
Many studies have shown the high efficacy of histamine H receptor ligands in preventing weight gain. In addition to evaluating the efficacy of future drug candidates, it is very important to assess their safety profile, which is established through numerous tests and preclinical studies. The purpose of the present study was to evaluate the safety of histamine H/sigma-2 receptor ligands by assessing their effects on locomotor activity and motor coordination, as well as on the cardiac function, blood pressure, and plasma activity of certain cellular enzymes. The ligands tested at a dose of 10 mg/kg b.w. did not cause changes in locomotor activity (except for KSK-74) and did not affect motor coordination. Significant reductions in blood pressure were observed after the administration of compounds KSK-63, KSK-73, and KSK-74, which seems logically related to the increased effect of histamine. Although the results of in vitro studies suggest that the tested ligands can block the human ether-a-go-go-related gene (hERG) potassium channels, they did not affect cardiac parameters in vivo. It should be noted that repeated administration of the tested compounds prevented an increase in the activity of alanine aminotransferase (AlaT) and gamma-glutamyl transpeptidases (gGT) observed in the control animals fed a palatable diet. The obtained results show that the ligands selected for this research are not only effective in preventing weight gain but also demonstrate safety in relation to the evaluated parameters, allowing the compounds to proceed to the next stages of research.
许多研究表明,组胺 H 受体配体在预防体重增加方面具有很高的疗效。除了评估未来候选药物的疗效外,评估其安全性概况也非常重要,这是通过大量测试和临床前研究建立的。本研究的目的是通过评估组胺 H/σ-2 受体配体对运动活性和运动协调性以及心脏功能、血压和某些细胞酶的血浆活性的影响来评估其安全性。在 10mg/kg bw 的剂量下测试的配体不会引起运动活性的变化(除了 KSK-74 之外),也不会影响运动协调性。在给予化合物 KSK-63、KSK-73 和 KSK-74 后,观察到血压显著降低,这似乎与组胺作用增强有关。尽管体外研究结果表明,所测试的配体可以阻断人 ether-a-go-go 相关基因 (hERG) 钾通道,但它们在体内不影响心脏参数。值得注意的是,反复给予测试化合物可防止在给予美味饮食的对照动物中观察到的丙氨酸氨基转移酶 (AlaT) 和γ-谷氨酰转肽酶 (gGT) 活性增加。所得结果表明,为这项研究选择的配体不仅在预防体重增加方面有效,而且在评估参数方面表现出安全性,使化合物能够进入下一阶段的研究。