The study of systematic, physiology, pharmacology and host-parasite relationship is compound by the lack of an efficient, simple and inexpensive method for anesthesia or muscle relaxing of gastropod molluscs.Pan (1958) demonstrated that snail exposition to a menthol solution produce muscle relaxation in pulmonate molluscs, allowing a better tissue fixation aiming histological analysis. Michelson (1958) demonstrated that the best snail distension and immobilization was obtained through the immersion of snail in urethan aqueous solution. This methodology has been largely used in many mollusc species, however the technique does not permit snail manipulation, which demands a complete state of anesthesia. Runhan et al. (1965) concluded that anesthetic or narcotic drugs have a variable effect on mollusc, depending on the mollusc species tested, the drug concentration and the exposition time. Planorbidae molluscs are routinely relaxed by sodium pentobarbital in taxonomical and
A new technique for fixation of Biomphalaria glabrata for histologic studies is described. It consists in performing several external holes in the shell, before placing the entire snail into the fixative. It is a very practical and quick procedure that showed excellent results when compared to the usual techniques.Key words: Biomphalaria glabrata -snail fixation -histologySince the pioneer studies related to the anatomy of the soft parts of planorbida, authors have been searching for a practical and rapid fixation method that would preserve the anatomical position of the mollusk inside the shell, as well as the anatomical structures of internal organs. Up to now, the methodology used in histology of planorbida utilizes menthol (Pan 1958) or urethane aqueous solution (Michelson 1958) aiming at obtaining muscular relaxation and exposition of the snail soft part. Anesthetized animals, with soft part exposed, are killed in warm water at 70°C (Borges et al. 1998). After the animal death in warm water, the columellar muscle is sectioned at the end of the spiral shell, the soft part removed and put into the fixative.Nowadays, the methodology used is time consuming (it is necessary several hours in menthol or urethane for muscular relaxation), the temperature of 70°C of warm water may denature snail proteins and damages the more sensitive anatomical structures. When the snails are infected with parasites, parasitic structures could be altered as well by the water temperature. In the present study a technique was developed in which anesthesia and warm water are not necessary for the process of fixation of Biomphalaria glabrata. The mollusk may be either infected or not with Schistosoma mansoni.Using a mini electric drilling machine (model 1-Dremel MFG Co., Racine WFS, USA) and 1 mm drill, small holes were made on the superior and inferior parts of the spiral shell and also in its lateral exposed parts. For a snail with 1 cm of shell diameter, it was necessary to perforate about 15 holes. It is important not to damage the internal membrane, to avoid bleeding and consequent shrinkage of the tissues. The procedure is also possible to be performed in snails smaller than 1 cm of shell diameter, such as B. straminea and juveniles of B. tenagophila or B. glabrata. However, in this case smaller drill should be used to avoid internal membrane damage.To test these new technique, normal or S. mansoniinfected B. glabrata, were anesthetized with pentobarbital [4 mg/l for 8 h, Martins-Souza et al. (2001)] to expose the soft parts of the snail, and then the shell holes were performed. The shell-perforated snails were placed into the fixative, i.e. phosphate-buffered 10% formalin for 24 h or Bouin´s fluid for 5 h, followed by washing in 70% alcohol. For comparison of the quality of fixation, normal and infected B. glabrata were anesthetized and fixed as described, but no shell holes were performed.Trying to obtain a faster and efficient snail fixation, another group of either normal or S. mansoni-infected B. glabrata was submitted to sh...
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