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1.
Braz. j. med. biol. res ; 39(8): 1137-1142, Aug. 2006. tab
Article in English | LILACS | ID: lil-433178

ABSTRACT

The physiopathology of obstructive sleep apnea-hypopnea syndrome (OSAHS) is multifactorial and obesity has been shown to be one of the main factors correlated with its occurrence. In obese patients with anatomical alterations of the upper airways it is often difficult to predict success for surgical correction since obesity is a limiting factor. Therefore, the aim of the present study was to evaluate the results of tonsillectomy in a specific group of patients, i.e., obese OSAHS patients with tonsil hypertrophy. Seven OSAHS patients with moderate obesity with obstructive palatine tonsil hypertrophy were submitted to tonsillectomy. All patients were submitted to pre- and postoperative appraisal of body mass index, otorhinolaryngology examination and polysomnography. Patients' average age was 36.4 ± 10.3 years and average preoperative body mass index was 36.6 ± 6.3 kg/m². Postoperative weight did not differ significantly from preoperative weight (P = 0.27). Average preoperative apnea and hypopnea index (AHI) was 81 ± 26/h and postoperative AHI was 23 ± 18/h (P = 0.0005). Average preoperative minimum oxyhemoglobin saturation (SaO2 min) was 69 ± 14 percent and the postoperative value was 83 ± 3 percent (P = 0.038). In relation to AHI, 6 (86 percent) of the 7 patients studied showed a reduction of 50 percent in relation to preoperative level and of these, 4 (57 percent) presented AHI of less than 20 percent. Only one patient presented a reduction of less than 50 percent in AHI, but even so showed improved SaO2 min. Tonsillectomy treatment for OSAHS in obese patients with obstructive palatine tonsil hypertrophy caused a significant reduction in AHI, with improvement in SaO2 min. This procedure could be eventually considered as an option of treatment for obese OSAHS patients with significant tonsil hypertrophy when continuous positive air pressure therapy is not possible as the first choice of treatment.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Obesity/complications , Sleep Apnea, Obstructive/etiology , Palatine Tonsil/pathology , Body Mass Index , Continuous Positive Airway Pressure , Hypertrophy/complications , Hypertrophy/surgery , Oxyhemoglobins/analysis , Polysomnography , Severity of Illness Index , Sleep Apnea, Obstructive/surgery , Tonsillectomy , Palatine Tonsil/surgery
2.
Braz. j. med. biol. res ; 38(3): 453-461, mar. 2005. graf
Article in English | LILACS | ID: lil-394796

ABSTRACT

Eucalyptol is an essential oil that relaxes bronchial and vascular smooth muscle although its direct actions on isolated myocardium have not been reported. We investigated a putative negative inotropic effect of the oil on left ventricular papillary muscles from male Wistar rats weighing 250 to 300 g, as well as its effects on isometric force, rate of force development, time parameters, post-rest potentiation, positive inotropic interventions produced by Ca2+ and isoproterenol, and on tetanic tension. The effects of 0.3 mM eucalyptol on myosin ATPase activity were also investigated. Eucalyptol (0.003 to 0.3 mM) reduced isometric tension, the rate of force development and time parameters. The oil reduced the force developed by steady-state contractions (50 percent at 0.3 mM) but did not alter sarcoplasmic reticulum function or post-rest contractions and produced a progressive increase in relative potentiation. Increased extracellular Ca2+ concentration (0.62 to 5 mM) and isoproterenol (20 nM) administration counteracted the negative inotropic effects of the oil. The activity of the contractile machinery evaluated by tetanic force development was reduced by 30 to 50 percent but myosin ATPase activity was not affected by eucalyptol (0.3 mM), supporting the idea of a reduction of sarcolemmal Ca2+ influx. The present results suggest that eucalyptol depresses force development, probably acting as a calcium channel blocker.


Subject(s)
Animals , Male , Rats , Cyclohexanols/pharmacology , Monoterpenes/pharmacology , Myocardial Contraction/drug effects , Oils, Volatile/pharmacology , Papillary Muscles/drug effects , Sarcoplasmic Reticulum/drug effects , Dose-Response Relationship, Drug , Drug Evaluation, Preclinical , Isometric Contraction/drug effects , Rats, Wistar , Skeletal Muscle Myosins/drug effects
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