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1.
Braz J Med Biol Res ; 51(6): e6602, 2018.
Article in English | MEDLINE | ID: mdl-29791594

ABSTRACT

The aim of this study was to investigate the reproductive, biochemical, and hematological outcomes of pregnant rats exposed to protein restriction. Wistar rat dams were fed a control normal-protein (NP, 17% protein, n=8) or a low-protein (LP, 8% protein, n=14) diet from the 1st to the 20th day of pregnancy. On the 20th day, the clinical signs of toxicity were evaluated. The pregnant rats were then anesthetized and blood samples were collected for biochemical-hematological analyses, and laparotomy was performed to evaluate reproductive parameters. No sign of toxicity, or differences (P>0.05) in body weight gain and biochemical parameters (urea, creatinine, albumin, globulin, and total protein) between NP and LP pregnant dams were observed. Similarly, hematological data, including red blood cell count, white blood cell count, hemoglobin, hematocrit, red blood cell distribution width (coefficient of variation), mean corpuscular volume, mean corpuscular hemoglobin, mean corpuscular hemoglobin concentration, % lymphocytes, absolute lymphocyte count, platelet count, and mean platelet volume were similar (P>0.05) at the end of pregnancy. Reproductive parameters (the dam-offspring relationship, ovary mass, placenta mass, number of corpora lutea, implantation index, resorption index, and the pre- and post-implantation loss rates) were also not different (P>0.05) between NP and LP pregnant dams. The present data showed that a protein-restricted diet during pregnancy did not alter reproductive, biochemical, and hematological parameters and seems not to have any toxic effect on pregnant Wistar rats.


Subject(s)
Adaptation, Physiological/physiology , Diet, Protein-Restricted/methods , Fetal Development/physiology , Genitalia, Female/physiology , Albumins/analysis , Animals , Creatinine/blood , Erythrocyte Count , Female , Globulins/analysis , Hematocrit , Hemoglobins/analysis , Leukocyte Count , Male , Pregnancy , Proteins/analysis , Rats , Rats, Wistar , Urea/blood , Weight Gain/physiology
2.
Nutr Metab Cardiovasc Dis ; 25(1): 123-30, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25287449

ABSTRACT

BACKGROUND AND AIMS: Maternal undernutrition induces development of the arterial hypertension. We investigated the effects of a maternal low-protein diet on cardiovascular autonomic control in the offspring. METHODS AND RESULTS: Male Wistar rats were divided into two groups according to the diets of their mothers during gestation and lactation: the control (normal protein, NP, 17% casein; n = 14) and low-protein (LP, 8% casein; n = 14) groups. Direct measurements of arterial pressure (AP) were recorded from wakeful 90-day-old male offspring. The LP offspring presented higher mean AP than did the NP rats (NP: 93 ± 4 vs. LP: 113 ± 2 mmHg; p < 0.05), whereas the heart rate (HR) was similar in the two groups. In the spectral analysis, the LP group showed higher power at low (NP: 1.98 ± 0.25 vs. LP: 3.7 ± 0.3 mmHg²; p < 0.05) and high (NP: 1.28 ± 0.18 vs. LP: 2.13 ± 0.42 mmHg²; p < 0.05) frequencies of systolic arterial pressure (SAP). In the pulse interval, the LP group presented an increase in the LF/HF ratio (NP: 0.32 vs. LP: 0.56; p < 0.05). After propranolol (4 mg/kg, intravenous (iv)), the bradycardia was higher in the LP group (NP: -36 ± 8 vs. LP: -94 ± 12 bpm; p < 0.05), after methylatropine (2 mg/kg, iv), the tachycardia was similar to NP group. After administration of the ganglionic blocker (hexamethonium; 25 mg/kg, iv), the LP animals showed larger delta variation in the AP (NP: -33.7 ± 5 vs. LP: -53.6 ± 4 mmHg; p < 0.05). CONCLUSION: The rats subjected to protein malnutrition presented an increase in the cardiovascular sympathetic tone, which contributed to the elevated AP observed in these animals.


Subject(s)
Autonomic Nervous System/physiopathology , Cardiovascular System/physiopathology , Diet, Protein-Restricted/adverse effects , Hypertension/etiology , Lactation , Maternal Nutritional Physiological Phenomena , Adrenergic beta-Antagonists/pharmacology , Animals , Autonomic Nervous System/drug effects , Bradycardia/chemically induced , Cardiovascular System/drug effects , Cardiovascular System/innervation , Drug Resistance , Female , Ganglionic Blockers/pharmacology , Heart Rate/drug effects , Hypertension/physiopathology , Male , Parasympatholytics/pharmacology , Pregnancy , Pulse Wave Analysis , Rats, Wistar , Sympatholytics/pharmacology , Tachycardia/chemically induced
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