Diabetes evolution in rats after neonatal treatment with alloxan.

Carla Ribeiro, Camila Aparecida Machado de Oliveira, Eliete Luciano, Maria Alice Rostom de Mello
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Abstract

Physical exercises have been recommended in the prevention of non-insulin dependent diabetes mellitus (NIDDM), but the mechanisms involved in this intervention are not yet fully understood. Experimental models offer the opportunity for the study of this matter. The present study was designed to analyze the diabetes evolution in rats submitted to neonatal treatment with alloxan with the objective of verifying the suitability of the model to future studies with exercises. For this, newly born rats (6 days old) received intraperitoneal alloxan (A=200 mg/kg of body weight). Rats injected with vehicle (citrate buffer) were used as controls (C). The fasting blood glucose level (mg/dL) was higher in the alloxan group at the day 28 (C=47.25 +/- 5.08; A=54.51 +/- 7.03) but not at the 60 day of age (C=69.18 +/- 8.31; A=66.81 +/- 6.08). The alloxan group presented higher blood glucose level during glucose tolerance test (GTT) (mg/dL. 120 min) in relation to the control group both at day 28 (C=16908.9 +/- 1078.8; A=21737.7 +/- 1106.4) and at day 60 (C=11463.45 +/- 655.30; A=15282.21 +/- 1221.84). Insulinaemia during GTT (ng/mL. 120 min) was lower at day 28 (C=158.67 +/- 33.34; A=123.90 +/- 19.80), but presented no difference at day 60 (C=118.83 +/- 26.02; A=97.88 +/- 10.88). At day 60, the glycogen concentration in the soleus muscle (mg/100 mg) was lower in the alloxan group (0.3 +/- 0.13) in relation to the control group (0.5 +/- 0.07). No difference was observed between groups in relation to (micromol/g.h): Glucose Uptake (C=5.8 +/- 0.63; A=5.2 +/- 0.73); Glucose Oxidation (C=4.3 +/- 1.13; A=3.9 +/- 0.44); Glycogen Synthesis (C=0.8 +/- 0.18; A=0.7 +/- 0.18) and Lactate Production (C=3.8 +/- 0.8; A=3.8 +/- 0.7) by the isolated soleus muscle. The glucose-stimulated insulin secretion (16.7mM) by the isolated islets (ng/5 islets. h) of the alloxan group was lower (14.3 +/- 4.7) than the control group (32.0 +/- 7.9). Thus, we may conclude that this neonatal diabetes induction model gathers interesting characteristics and may be useful for further studies on the role of the exercise in the diabetes mellitus appearance.

新生儿四氧嘧啶治疗后大鼠糖尿病的演变。
体育锻炼已被推荐用于预防非胰岛素依赖型糖尿病(NIDDM),但其干预机制尚不完全清楚。实验模型为研究这一问题提供了机会。本研究旨在分析新生大鼠接受四氧嘧啶治疗后的糖尿病演变,目的是验证该模型在未来运动研究中的适用性。为此,新生大鼠(6日龄)腹腔注射四氧嘧啶(A=200 mg/kg体重)。四氧嘧啶组大鼠第28天空腹血糖水平(mg/dL)较高(C=47.25 +/- 5.08;A=54.51 +/- 7.03),但60日龄时无明显差异(C=69.18 +/- 8.31;A=66.81 +/- 6.08)。葡萄糖耐量试验(GTT) (mg/dL)时,四氧嘧啶组血糖升高。(C=16908.9 +/- 1078.8;A=21737.7 +/- 1106.4)和第60天(C=11463.45 +/- 655.30;A=15282.21 +/- 1221.84)。GTT期间胰岛素血症(ng/mL)。120 min)在第28天降低(C=158.67 +/- 33.34;A=123.90 +/- 19.80),但在第60天无差异(C=118.83 +/- 26.02;A=97.88 +/- 10.88)。第60天,四氧嘧啶组比目鱼肌糖原浓度(mg/100 mg)(0.3 +/- 0.13)低于对照组(0.5 +/- 0.07)。(微摩尔/g.h):葡萄糖摄取(C=5.8 +/- 0.63;A=5.2 +/- 0.73);葡萄糖氧化(C=4.3 +/- 1.13;A=3.9 +/- 0.44);糖原合成(C=0.8 +/- 0.18;A=0.7 +/- 0.18)和乳酸产量(C=3.8 +/- 0.8;A=3.8 +/- 0.7)。离体胰岛(ng/5)葡萄糖刺激胰岛素分泌(16.7mM)。四氧嘧啶组的H值(14.3 +/- 4.7)低于对照组(32.0 +/- 7.9)。因此,我们可以得出结论,该新生儿糖尿病诱导模型收集了有趣的特征,可能有助于进一步研究运动在糖尿病出现中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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