Preliminary evaluation of the efficacy and safety of brimonidine for deep sedation DOI
Xiaohui Wang, Rui Zhang, Bin Chen

et al.

Fundamental and Clinical Pharmacology, Journal Year: 2023, Volume and Issue: 38(1), P. 139 - 151

Published: Aug. 23, 2023

Abstract Background Although brimonidine is currently used in the clinical treatment of glaucoma and rosacea, research deep sedative effect on animals after systemic administration reported firstly has shown promising results. Methods The median effective dose (ED 50 ), lethal (LD therapeutic index for sedation formalin stimulation assay were determined by various animal experiments. synergistic anesthesia rabbits with chloral hydrate was preliminarily evaluated. Results ED highly intraperitoneal injection rats calculated to be 2.05 mg kg −1 a 95% confidence interval (CI) 1.87 2.25 . intravenous intrarectal 0.087 CI 0.084 0.091 1.65 1.43 1.91 , respectively. LD 468 441 497 228. Brimonidine certain analgesic heart rate lowering effects. Conclusion results confirmed that effects high safety. It can combination other types drugs achieve better

Language: Английский

Designing Chromane Derivatives as α2A-Adrenoceptor Selective Agonists via Conformation Constraint DOI
Xucheng Lv,

Peilan Zhou,

Xuehong Qiao

et al.

Journal of Medicinal Chemistry, Journal Year: 2024, Volume and Issue: 67(13), P. 11435 - 11449

Published: June 18, 2024

Enhancing the selectivity of alpha2-adrenoceptor (α2A-AR) agonists remains an unresolved issue. Herein, we reported design α2A-AR agonist using conformation constraint method, beginning with medetomidine. The structure–activity relationship indicated that 8-substituent chromane derivatives exerted most pronounced effect on agonistic activity. Compounds A9 and B9 were identified as promising, exhibiting EC50 values 0.78 0.23 nM, respectively. Their indexes surpassed dexmedetomidine (DMED) by 10–80 fold. In vivo studies demonstrated both dose-dependently increased loss righting reflex in mice, ED50 1.54 0.138 mg/kg, Binding mode calculations mutation suggested indispensability hydrogen bond between ASP1283.32 agonist. particular, showed no dual reverse pharmacological effect, a characteristic exhibited DMED activation.

Language: Английский

Citations

1

Advances in the use of dexmedetomidine for postoperative cognitive dysfunction DOI Creative Commons
Meng Deng, Yuan Wang, B. Zheng

et al.

Anesthesiology and Perioperative Science, Journal Year: 2024, Volume and Issue: 2(4)

Published: Oct. 30, 2024

Abstract Postoperative cognitive dysfunction, a common neurological complication in the perioperative period, seriously affects patient survival and prognosis. Its high incidence has made study of postoperative dysfunction challenging. Whether clinical application dexmedetomidine, potential neuroprotective drug, can reduce is controversial, although several mechanisms by which dexmedetomidine improves have been identified; therefore, this remains an area need further exploration.

Language: Английский

Citations

1

Dexmedetomidine modulates neuronal activity of horizontal limbs of diagonal band via α2 adrenergic receptor in mice DOI Creative Commons

Xia-wei Zhang,

Lei Chen, Changfeng Chen

et al.

BMC Anesthesiology, Journal Year: 2023, Volume and Issue: 23(1)

Published: Oct. 2, 2023

Abstract Background and objectives Dexmedetomidine (DEX) is widely used in clinical sedation which has little effect on cardiopulmonary inhibition, however the mechanism remains to be elucidated. The basal forebrain (BF) a key nucleus that controls sleep-wake cycle. horizontal limbs of diagonal bundle (HDB) one subregions BF. purpose this study was examine whether possible DEX through α2 adrenergic receptor BF (HDB). Methods In study, we investigated effects by using whole cell patch clamp recordings. threshold stimulus intensity, inter-spike-intervals (ISIs) frequency action potential firing neurons were recorded application (2 µM) co-application α 2 antagonist phentolamine (PHEN) (10 µM). Results increased inhibited enlarged inter-spike-interval (ISI) neurons. These reversed PHEN Conclusion Taken together, our findings revealed decreased discharge activity neuron via receptors.

Language: Английский

Citations

2

Signalling of Adrenoceptors: Canonical Pathways and New Paradigms DOI

Chantel Mastos,

Xiaomeng Xu, Alastair C. Keen

et al.

Handbook of experimental pharmacology, Journal Year: 2024, Volume and Issue: unknown

Published: Jan. 1, 2024

Language: Английский

Citations

0

Asthma and COPD: A Focus on β-Agonists – Past, Present and Future DOI
Jillian G. Baker, Dominick Shaw

Handbook of experimental pharmacology, Journal Year: 2023, Volume and Issue: unknown

Published: Jan. 1, 2023

Language: Английский

Citations

1

Preliminary evaluation of the efficacy and safety of brimonidine for deep sedation DOI
Xiaohui Wang, Rui Zhang, Bin Chen

et al.

Fundamental and Clinical Pharmacology, Journal Year: 2023, Volume and Issue: 38(1), P. 139 - 151

Published: Aug. 23, 2023

Abstract Background Although brimonidine is currently used in the clinical treatment of glaucoma and rosacea, research deep sedative effect on animals after systemic administration reported firstly has shown promising results. Methods The median effective dose (ED 50 ), lethal (LD therapeutic index for sedation formalin stimulation assay were determined by various animal experiments. synergistic anesthesia rabbits with chloral hydrate was preliminarily evaluated. Results ED highly intraperitoneal injection rats calculated to be 2.05 mg kg −1 a 95% confidence interval (CI) 1.87 2.25 . intravenous intrarectal 0.087 CI 0.084 0.091 1.65 1.43 1.91 , respectively. LD 468 441 497 228. Brimonidine certain analgesic heart rate lowering effects. Conclusion results confirmed that effects high safety. It can combination other types drugs achieve better

Language: Английский

Citations

0