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1.
J Pediatr Endocrinol Metab ; 19(5): 713-26, 2006 May.
Article in English | MEDLINE | ID: mdl-16789638

ABSTRACT

This study was designed to determine the relationship of dimensions, wall thickness and function of the left ventricle with diabetes duration, fasting blood glucose, lipid profile, beta-OH-butyrate, free fatty acids (FFA) and carnitine levels in children and adolescents with type 1 diabetes mellitus (DM1) who had no cardiovascular complications. Thirty-five patients with DM1 (18 F/17 M, mean age: 12.0 years) and age matched control children (n = 24) were enrolled in the study. Patients with DM1 were subdivided into Group I (mean DM1 duration 3.5 years, n = 14), and Group II (mean DM1 duration 8.2 years, n = 21). Dimensions, wall thickness and systolic functions of the left ventricle were normal in all patients with DM1. Diastolic functions were normal in Group I. In Group II, peak A wave velocity (AVEL) (p = 0.004), velocity-time integral of A wave (AVTI) (p = 0.007) and isovolumetric relaxation time corrected by heart rate (cIVRT) (p = 0.048) were high, and peak E wave velocity (EVEL) and velocity-time integral of E wave (EVTI) were normal. E/A (p < 0.0001) and EVTI/AVTI (p = 0.001) were low in this group. In Group I, systolic and diastolic blood pressure, HDL-cholesterol and FFA values were normal; total cholesterol (p = 0.047), LDL-cholesterol (p = 0.017), beta-OH-butyrate (p = 0.003), and acetyl carnitine (p = 0.006) levels were high. In Group II, diastolic blood pressure (p = 0.008), total cholesterol (p < 0.0001) and LDL-cholesterol (p < 0.0001) were increased; and total carnitine (p = 0.019), free carnitine (p = 0.002) and HDL-cholesterol (p = 0.039) were decreased. Correlations were detected between total carnitine and AVEL and HR; free carnitine and AVEL, E/A and HR; HbA1c and EVTI/AVTI and cIVRT; LDL-cholesterol and E/A, EVTI/AVTI ratios and cIVRT; HDL-cholesterol and AVEL; FFA and LVDD, IVSD, LVPWD, LVmass and CO; metabolic parameters and DM1 duration and echocardiographic findings such as AVEL, EVEL, EVTI, VmaxAV and CO. In conclusion, left ventricular dimensions, wall thickness and systolic functions were normal in children and adolescents with DM1 who had no obvious cardiovascular complications. Left ventricular diastolic functions were abnormal in patients of Group II. Left ventricular diastolic function abnormalities were associated with glycemic control, free and total carnitine, and LDL- and HDL-cholesterol levels.


Subject(s)
Cardiomyopathies/etiology , Diabetes Complications/physiopathology , Diabetes Mellitus, Type 1/physiopathology , Adolescent , Adult , Blood Glucose/metabolism , Cardiomyopathies/diagnostic imaging , Carnitine/blood , Child , Child, Preschool , Cholesterol/blood , Diabetes Complications/diagnostic imaging , Diabetes Mellitus, Type 1/diagnostic imaging , Diabetes Mellitus, Type 1/metabolism , Diastole/physiology , Echocardiography , Echocardiography, Doppler , Female , Heart Function Tests , Humans , Infant , Lipids/blood , Male , Systole/physiology
2.
J Toxicol Environ Health A ; 67(13): 979-86, 2004 Jul 09.
Article in English | MEDLINE | ID: mdl-15205029

ABSTRACT

The aim of this study was to determine the effects of streptozotocin-induced diabetes on plasma reduced glutathione (GSH) and S-nitrosoglutathione (GSNO) levels. Further, the study investigated whether an antioxidant, pineal hormone melatonin, could protect against STZ-induced effects. STZ significantly decreased plasma GSH but increased the levels of plasma GSNO. Daily supplementation with melatonin restored plasma thiol to control values. Data suggest that STZ-induced hyperglycemia and compounds that act as scavengers of free radicals and peroxynitrite like melatonin may exert protection against STZ-induced toxicity.


Subject(s)
Antioxidants/pharmacology , Diabetes Mellitus, Experimental/drug therapy , Dietary Supplements , Glutathione/blood , Melatonin/pharmacology , S-Nitrosoglutathione/blood , Animals , Antioxidants/administration & dosage , Antioxidants/therapeutic use , Diabetes Mellitus, Experimental/blood , Diabetes Mellitus, Experimental/chemically induced , Male , Melatonin/administration & dosage , Melatonin/therapeutic use , Rats , Rats, Wistar , Streptozocin
3.
Paediatr Anaesth ; 13(6): 508-14, 2003 Jul.
Article in English | MEDLINE | ID: mdl-12846707

ABSTRACT

BACKGROUND: Although the use of opioids during general anaesthesia suppresses stress response to surgery and pain, the effects on antidiuretic hormone (ADH) are controversial. The aim of this study was to find the effects of morphine with either intravenous infusion or epidural route on ADH and other stress hormones. METHODS: Fifty children aging (1-15 years) undergoing major genito-urinary or abdominal operations were included in this study. The patients were allocated randomly to two groups receiving either a single dose of epidural morphine 0.1 mg.kg-1 (EP group, n = 25) postinduction or morphine infusion (INF group; n = 25) at 0.02 mg.kg-1.h-1 following 0.05 mg.kg-1 bolus. Blood samples were withdrawn for plasma ADH, osmolality, glucose, cortisol, insulin and morphine level analysis following induction and 1, 5, 12 and 24 h after initial morphine administration. RESULTS: The two groups were similar in demographic factors, pain scores, sedation scores, and incidence of nausea and vomiting. The amount of morphine received was different between groups and the changes in serum levels of morphine were statistically significant in EP group ( P < 0.05). The changes in cortisol, blood glucose and insulin levels were insignificant in both groups (P > 0.05). The changes of ADH levels were significant at time-points in both groups, reaching control levels at the 24th hour (P < 0.05). CONCLUSION: Despite the effective pain therapy and suppression of cortisol and insulin response to surgical stimulus, the increase in ADH secretion is not effected by systemic or epidural morphine administration.


Subject(s)
Analgesia, Epidural , Analgesics, Opioid/administration & dosage , Analgesics, Opioid/adverse effects , Morphine/administration & dosage , Morphine/adverse effects , Vasopressins/blood , Abdomen/surgery , Adolescent , Analgesics, Opioid/therapeutic use , Blood Glucose/metabolism , Child , Child, Preschool , Female , Hormones/blood , Humans , Hydrocortisone/blood , Infant , Infusions, Intravenous , Insulin/blood , Male , Morphine/therapeutic use , Pain Measurement , Pain, Postoperative/drug therapy , Surgical Procedures, Operative , Tachycardia/chemically induced , Tachycardia/epidemiology , Urogenital Surgical Procedures
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