GABA(A) receptor-targeted drug development -New perspectives in perioperative anesthesia

被引:26
作者
Antkowiak, Bernd [1 ,2 ]
Rammes, Gerhard [3 ]
机构
[1] Eberhard Karls Univ Tubingen, Dept Anesthesiol & Intens Care, Expt Anesthesiol Sect, Waldhornlestr 22, D-72072 Tubingen, Germany
[2] Werner Reichardt Ctr Integrat Neurosci, Dept Anaesthesiol & Intens Care, Expt Anaesthesiol Sect, Tubingen, Germany
[3] Univ Hosp Rechts Isar, Dept Anesthesiol, Munich, Germany
关键词
Benzodiazepine; translocator protein; neurosteroid; propofol; etomidate; cognitive dysfunction; chronic pain; GAMMA-AMINOBUTYRIC-ACID; 18 KDA TSPO; PERIPHERAL BENZODIAZEPINE-RECEPTOR; LONG-TERM POTENTIATION; POSITIVE ALLOSTERIC MODULATOR; HIPPOCAMPAL HT-22 CELLS; LOW BISPECTRAL INDEX; A RECEPTOR; DELTA-SUBUNIT; NEUROSTEROID MODULATION;
D O I
10.1080/17460441.2019.1599356
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Perioperative anesthesia delivers pre-, intra-, and postoperative care to meet the needs of patients undergoing diagnostic and surgical procedures. Major challenges are patients at the extremes of age and individuals with a pre-existing disease burden. Frequent problems are the development of chronic pain and cognitive dysfunction upon surgery. Current perioperative pharmacotherapy utilizes a number of drugs acting at GABA(A) receptors. Area covered: This review evaluates novel formulations and newly designed GABAergic drugs, offering future improvements in perioperative anesthesia, especially for reducing mortality and avoiding cognitive dysfunction and chronic pain as an outcome of surgery. Expert opinion: There are multiple reasons for mounting efforts in the development of novel GABAergic medications. First, requirements in perioperative anesthesia care have substantially changed during the last two decades. In this respect, the dramatic increase in life expectancy is the most important factor. Moreover, research has considerably expanded our knowledge of how drugs in current clinical use act on the molecular level. Almost all ongoing developmental programs choose chemical structures of well-tried agents as a starting point for exploring the properties of structural analogs. This strategy aims to maintain the clinically desired actions of mother compounds while attempting to extinguish adverse side effects.
引用
收藏
页码:683 / 699
页数:17
相关论文
共 240 条
[1]   Characterization of brain neurons that express enzymes mediating neurosteroid biosynthesis [J].
Agis-Balboa, Roberto C. ;
Pinna, Graziano ;
Zhubi, Adrian ;
Maloku, Ekrem ;
Veldic, Marin ;
Costa, Erminio ;
Guidotti, Alessandro .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (39) :14602-14607
[2]   ADRENOCORTICAL SUPPRESSION BY A SINGLE INDUCTION DOSE OF ETOMIDATE [J].
ALLOLIO, B ;
STUTTMANN, R ;
LEONHARD, U ;
FISCHER, H ;
WINKELMANN, W .
KLINISCHE WOCHENSCHRIFT, 1984, 62 (21) :1014-1017
[3]   New insights in the systemic and molecular underpinnings of general anesthetic actions mediated by γ-aminobutyric acid A receptors [J].
Antkowiak, Bernd ;
Rudolph, Uwe .
CURRENT OPINION IN ANESTHESIOLOGY, 2016, 29 (04) :447-453
[4]   Reduction and prevention of vincristine-induced neuropathic pain symptoms by the non-benzodiazepine anxiolytic etifoxine are mediated by 3α-reduced neurosteroids [J].
Aouad, Maya ;
Charlet, Alexandre ;
Rodeau, Jean-Luc ;
Poisbeau, Pierrick .
PAIN, 2009, 147 (1-3) :54-59
[5]  
Atack JR, 2011, CURR TOP MED CHEM, V11, P1203
[6]   Differential depression of neuronal network activity by midazolam and its main metabolite 1-hydroxymidazolam in cultured neocortical slices [J].
Balk, Monika ;
Hentschke, Harald ;
Rudolph, Uwe ;
Antkowiak, Bernd ;
Drexler, Berthold .
SCIENTIFIC REPORTS, 2017, 7
[7]  
Barnard EA, 1998, PHARMACOL REV, V50, P291
[8]   Ligand for Translocator Protein Reverses Pathology in a Mouse Model of Alzheimer's Disease [J].
Barron, Anna M. ;
Garcia-Segura, Luis M. ;
Caruso, Donatella ;
Jayaraman, Anusha ;
Lee, Joo-Won ;
Melcangi, Roberto C. ;
Pike, Christian J. .
JOURNAL OF NEUROSCIENCE, 2013, 33 (20) :8891-8897
[9]   PROLONGED SEDATION DUE TO ACCUMULATION OF CONJUGATED METABOLITES OF MIDAZOLAM [J].
BAUER, TM ;
RITZ, R ;
HABERTHUR, C ;
HA, HR ;
HUNKELER, W ;
SLEIGHT, AJ ;
SCOLLOLAVIZZARI, G ;
HAEFELI, WE .
LANCET, 1995, 346 (8968) :145-147
[10]   The interaction of the general anesthetic etomidate with the gamma-aminobutyric acid type A receptor is influenced by a single amino acid [J].
Belelli, D ;
Lambert, JJ ;
Peters, JA ;
Wafford, K ;
Whiting, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (20) :11031-11036