PubMed · 11217994
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A Metin, O Calka, L Behçet, E Yildirim. 2001. Phytodermatitis from Ranunculus damascenus.. https://doi.org/10.1034/j.1600-0536.2001.440308-4.x
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The circulatory system of adult blue crabs, Callinectes sapidus, was mapped by either injecting barium sulfate into intact animals followed by radiography or by resin corrosion casts (Batsons Monomer). Seven arteries arise from the heart. The anterior aorta exits from the anterior dorsal surface of the heart and gives rise to the optic arteries; these arteries supply hemolymph to the supraesophageal ganglion and eyestalks. The paired anterolateral arteries also exit from the anterior dorsal surface of the heart and supply hemolymph to the gonads, hepatopancreas, stomach, antennal gland, mandibular muscles, and the hypodermis of the anterior cephalothorax. The paired hepatic arteries exit the heart anteriorly and ventrally and branch profusely within the hepatopancreas. A smaller side branch, the pyloric hepatic artery, supplies hemolymph to the pyloric stomach and midgut. The smallest artery, the posterior aorta, branches off the posterior ventral surface of the heart; it joins with the inferior abdominal artery in the region of the second abdominal segment and these arteries supply hemolymph to the hindgut and abdomen. The largest artery is the sternal artery, which exits from the ventral surface of the heart; the ventral thoracic artery branches off the sternal artery and supplies hemolymph to the chelae, the mouthparts, and to each pereiopod. The present study shows that the circulatory system is highly developed, with arteries dividing into smaller capillary-like vessels that ramify profusely within individual organs. The return vessels, the sinuses, are discrete channels rather than random open spaces, as previously described. The present study refines and advances descriptions of the circulatory system and is discussed in relation to recent work on hemolymph flow in crustaceans.
Three retinaldehyde dehydrogenases (RALDH1, RALDH2 and RALDH3), which catalyze the oxidation of retinaldehyde into retinoic acid, have been shown to be differentially expressed during early embryogenesis. Here, we report their differential expression patterns throughout later mouse organogenesis. Raldh1 is prominently expressed in developing lung (notably in bronchial and tracheal epithelia), and shows stage-specific expression in stomach and intestine epithelial and mesenchymal layers. Raldh3 expression is specific to the differentiating intestinal lamina propria. Raldh2 is expressed throughout the kidney nephrogenic zone, whereas Raldh1 and Raldh3 are mostly expressed in collecting duct epithelia. Raldh3 expression is more restricted than that of Raldh1 in the urogenital tract and sex gland epithelia, whereas Raldh2 expression is mesenchymal. Raldh1 is coexpressed with Raldh2 in the early heart epicardium, and is later specifically expressed in developing heart valves. All three genes exhibit distinct expression patterns in respiratory and olfactory epithelia and/or mesenchymes, and in developing teeth. Only Raldh1 expression is seen after birth in specific brain structures. These data indicate a requirement for regulated RA synthesis in various differentiating organs.
UNLABELLED: We designed this study to assess the efficacy of dolasetron compared with clonidine and placebo in prophylaxis of postanesthetic shivering. We included 90 patients undergoing elective abdominal or urologic surgery. The patients were randomly assigned to one three groups (each group n = 30) using a double-blinded study protocol: Group A received 12.5 mg dolasetron, Group B 3 microg/kg clonidine, and Group C saline 0.9% as placebo. The medication was given after the induction of anesthesia. Postanesthetic shivering was judged by using a five-point scale. In the Clonidine group, 86.6% showed no shivering, whereas in the Dolasetron and Placebo groups, only 63.3% and 66.6%, respectively, were symptom free. Only clonidine, but not dolasetron, significantly reduced the incidence and the severity of shivering. We conclude that clonidine is effective in preventing shivering when given before surgery, whereas dolasetron, at the dose used, is not effective. IMPLICATIONS: Shivering, an irregular muscular fasciculation lasting longer than 15 s, is a common complication secondary to general anesthesia. We compared dolasetron with clonidine (an established antishivering drug) in the prevention of postanesthetic shivering. Dolasetron 12.5 mg was not effective.