戊巴比妥麻醉与盐酸美托咪定、咪达唑仑、酒石酸丁托啡诺联用麻醉对自发性糖尿病Torii脂肪大鼠视网膜电图影响的差异。

Biomedicine Hub Pub Date : 2022-09-01 DOI:10.1159/000526189
Tetsuya Hasegawa, Rina Takagi, Yoshiaki Tanaka, Takeshi Ohta, Masami Shinohara, Yasushi Kageyama, Tomohiko Sasase, Shin-Ichi Muramatsu, Toshikatsu Kaburaki, Akihiro Kakehashi
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引用次数: 1

摘要

目的:探讨不同麻醉药物对自发性糖尿病Torii脂肪大鼠视网膜电图(ERGs)的影响。方法:12只9周龄正常SD大鼠(Jcl:SD大鼠)和16只SDT肥胖大鼠在戊巴比妥全麻或盐酸美托咪定、咪达唑仑、酒石酸布托啡诺(MMB)复合麻醉下的ERG记录。每只动物模型分为戊巴比妥组和MMB组。测量了a波和b波的振幅和峰值时间以及振荡电位(OPs)从0.0001坎德拉/平方米(cd.s/m2)到10.0 cd.s/m2。结果:Jcl:SD大鼠MMB组a波振幅明显升高,而两组SDT脂肪大鼠振幅差异无统计学意义。Jcl:SD两组大鼠的OP1振幅差异无统计学意义,但SDT脂肪大鼠MMB组的OP1振幅明显升高。在Jcl:SD大鼠和SDT脂肪大鼠中,戊巴比妥组的OP2振幅均显著升高。在Jcl:SD和SDT脂肪大鼠组之间,OP3振幅无显著差异。对于Jcl:SD和SDT脂肪大鼠,MMB组的OP4波振幅均显著升高。在Jcl:SD和SDT脂肪大鼠组之间,OP1和OP4的振幅总和(ΣOPs)无显著差异。Jcl:SD组大鼠b波振幅差异无统计学意义,但戊巴比妥治疗的SDT脂肪大鼠b波振幅明显升高。戊巴比妥组SD大鼠a波、OP1、OP2、OP3、OP4、ΣOPs的峰值时间明显延长。Jcl:SD大鼠MMB组b波峰值时间明显延长,但SDT脂肪大鼠除a波无显著差异外,结果相同。结论:ERG结果随麻醉药物的不同而不同。在使用MMB时,可以详细观察OPs。由于SDT肥胖大鼠是糖尿病模型动物,在详细研究OP波时,我们推荐MMB作为麻醉的选择。
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Differences in the Effects of Pentobarbital Anesthetic and Combination of Medetomidine Hydrochloride, Midazolam, and Butorphanol Tartrate Anesthetic on Electroretinogram in Spontaneously Diabetic Torii Fatty Rats.

Purpose: The aim of this study was to investigate the effects of different anesthetic agents on electroretinograms (ERGs) in Spontaneously Diabetic Torii fatty rats (SDT fatty rats).

Methods: The ERG recordings were measured under general anesthesia using pentobarbital or a combination of medetomidine hydrochloride, midazolam, and butorphanol (MMB) tartrate anesthesia in 12 9-week-old normal Sprague-Dawley rats (Jcl:SD rats) and 16 SDT fatty rats. Each animal model was divided into 2 groups, the pentobarbital group and MMB group. The amplitudes and peak times of the a- and b-waves and oscillatory potentials (OPs) were measured from 0.0001 candela per square meter (cd.s/m2) to 10.0 cd.s/m2.

Results: The amplitude of the a-wave was significantly higher in the MMB group of Jcl:SD rats, but there was no significant difference in amplitude between the two groups of SDT fatty rats. There was no significant difference in the OP1 amplitude between both groups of Jcl:SD rats, but the OP1 amplitude was significantly higher in the MMB group of SDT fatty rats. The OP2 amplitude was significantly higher in the pentobarbital group in both the Jcl:SD rats and SDT fatty rats. There was no significant difference in the OP3 amplitude between the Jcl:SD and SDT fatty rat groups. The amplitude of the OP4 waves was significantly higher in the MMB group for both Jcl:SD and SDT fatty rats. There was no significant difference in the sums of the OP1 to OP4 (ΣOPs) amplitudes between the Jcl:SD and SDT fatty rat groups. There was no significant difference in the b-wave amplitude between the Jcl:SD rat groups, but the b-wave amplitude was significantly higher in the SDT fatty rats that received pentobarbital. The peak times for a-wave, OP1, OP2, OP3, OP4, and ΣOPs were significantly longer in the pentobarbital group of SD rats. The peak time of the b-wave was significantly longer in the MMB group of Jcl:SD rats, but the same result was obtained in the SDT fatty rats except that there was no significant difference in the a-wave.

Conclusion: The overall ERG results vary depending on the anesthetic agent used. The OPs can be observed in detail when using MMB. Since the SDT fatty rat is a diabetic model animal, we recommend MMB as the anesthesia of choice when studying the OP waves in detail.

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