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Neuroteratology studies in rats: effects of feed restriction and monocrotaline

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Author(s):
Esther Lopes Ricci Adari Camargo
Total Authors: 1
Document type: Master's Dissertation
Press: São Paulo.
Institution: Universidade de São Paulo (USP). Faculdade de Medicina Veterinária e Zootecnia (FMVZ/SBD)
Defense date:
Examining board members:
Helenice de Souza Spinosa; Silvana Lima Gorniak; Miriam Oliveira Ribeiro
Advisor: Helenice de Souza Spinosa
Abstract

The problems caused by the exposure of animals to plants in Brazil dates from the early days of colonization, in particular, plants of the genus Crotalaria. These plants can be found worldwide, mainly distributed in tropical and subtropical areas; its main active principle is the pyrrolizidine alkaloid monocrotaline (MCT), which is found in their seeds and aerial parts. In the present study it was evaluated the acute toxicity of MCT, as the effects of exposure during pregnancy and the different doses of MCT on the physical and neurobehavioral development of rat offsprings. In addition, we also studied the effects of feed restriction (FR) in pregnant rats and their offspring since previous data from our laboratory showed that the MCT decreased body weight of rats treated for 14 days. Thus, Wistar rats were subjected to feed restriction during the 6th to 20th day of gestation, receiving 85, 60, 45 or 30% of average daily feed intake (100% = 22.75 g diet). The data showed that RF: a) promoted maternal cannibalism dependent on the intensity of the RA\'s mother, knowing that the largest group of restriction (30%) no offspring survived, b) it reduced the body weight of offspring, but this effect was observed from day 14 of life in the offspring from rats with 45% FR and 35 days of life in the offspring of rats from groups 60, 45 and 30% of FR, c) in the assessment of physical development of offspring no changes were observed between groups, except the body weight of offspring, d) neurobehavioral evaluation was observed reduction only in the general activity of the offspring and this effects being dependent on the severity of RA. The MCT (10, 30 and 100 mg / kg) administered as a single dose in rats and pregnant rats caused alterations in the scores of clinical dose-dependent and pregnant females were shown to be more sensitive to the toxic effects of MCT than virgin females and males. Exposure to MCT (1.0, 3.5 and 7.0 mg / kg) during pregnancy promoted: a) reduction on the number of pups born of mothers who received 3.5 and 7.0 mg / kg when compared to mothers and controls pair-feeding (group received the same amount of feed consumed by the group treated with the highest MCT), b) reduction of body weight of offspring of the group that received 1.0 and 7.0 mg / kg from the 35th day of life, c) on the evaluation of the physical development of offspring no changes were observed between groups, except the body weight of offspring, d) on neurobehavioral evaluation it was observed increase of immobility only in the time. These were measured on the open field of the offspring of mothers who received 3.5 and 7.0 mg / kg MCT. The present findings revealed that RA has a minor role in the toxicity of MCT, showing no close correlation between maternal weight loss and development of offspring exposed to toxin and RA. The inclusion of the pair-feeding group appears to be important when regards the toxicity studies of development, knowing that this can represent a control of the nutritional aspects involved in the test. It also suggest that in the protocols of toxicity development evaluation be included studies of mother-cub and the late development of offspring exposed. (AU)