Streptozotocin Diabetes Attenuates the Effects of Nondepolarizing Neuromuscular Relaxants on Rat Muscles.
10.4196/kjpp.2014.18.6.461
- Author:
Lina HUANG
1
;
Dan CHEN
;
Shitong LI
Author Information
1. Department of Anesthesiology, The Affiliated First People's Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200080, China. bravespirit.li@gmail.com
- Publication Type:Original Article
- Keywords:
Diabetes;
Extensor digitorum longus;
Non-depolarizing muscle relaxants;
Soleus;
Streptozotocin
- MeSH:
Animals;
Diabetes Mellitus, Experimental*;
Inhibitory Concentration 50;
Muscles*;
Neuromuscular Blockade;
Neuromuscular Junction;
Neuromuscular Nondepolarizing Agents;
Rats*;
Streptozocin;
Vecuronium Bromide
- From:The Korean Journal of Physiology and Pharmacology
2014;18(6):461-467
- CountryRepublic of Korea
- Language:English
-
Abstract:
The hypothesis of this study was that diabetes-induced desensitization of rat soleus (SOL) and extensor digitorum longus (EDL) to non-depolarizing muscle relaxants (NDMRs) depends on the stage of diabetes and on the kind of NDMRs. We tested the different magnitude of resistance to vecuronium, cisatracurium, and rocuronium at different stages of streptozotocin (STZ)-induced diabetes by the EDL sciatic nerve-muscle preparations, and the SOL sciatic nerve-muscle preparations from rats after 4 and 16 weeks of STZ treatment. The concentration-twitch tension curves were significantly shifted from those of the control group to the right in the diabetic groups. Concentration giving 50% of maximal inhibition (IC50) was larger in the diabetic groups for all the NDMRs. For rocuronium and cisatracurium in both SOL and EDL, IC50 was significantly larger in diabetic 16 weeks group than those in the diabetic 4 weeks group. For SOL/EDL, the IC50 ratios were significantly largest in the diabetic 16 weeks group, second largest in the diabetic 4 weeks group, and smallest for the control group. Diabetes-induced desensitization to NDMRs depended on the stage of diabetes and on the different kind of muscles observed while was independent on different kind of NDMRs. The resistance to NDMRs was stronger in the later stage of diabetes (16 versus 4 weeks after STZ treatment). Additionally, when monitoring in SOL, diabetes attenuated the actions of neuromuscular blockade more intensely than that in EDL. Nonetheless, the hyposensitivity to NDMRs in diabetes was not relevant for the kind of NDMRs.
