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Biomedical subjects

F García

Publications and source records attributed to F García.

At least 181 records · Page 10Linked to original sources

The quality and extension of nerve fibre regeneration in the centrocentral anastomosis of the peripheral nerve.

Centro central anastomosis (CCA) is the connection created by means of a nerve autograft placed between the fascicles of the proximal stump of a sectioned nerve. We have used this technique in the laboratory and in the human to avoid the formation of a terminal neuroma after amputation of a limb. The aim of the present study is to know what is the quality and how long is the progression of the regenerating nerve fibers coming from a fascicle and growing inside the nerve graft and into the other central fascicle. 56 male, adult, Sprague-Dawley rats were operated on. The 4 rats of Group I were used for control: the right sciatic nerve was exposed and dissected in its four branches. One piece of 10 mm was taken of each of the sural and the peroneal branches for hystological and histomorphometric studies. In the 16 rats of Group II, after the section of the sural and peroneal branches a terminoterminal suture between their proximal stumps was made. In the 16 rats of Group III a CCA with an interposed nerve graft of 7 mm was achieved. 5.5 and 6 rats of Groups II and III were sacrificed at 10, 40 and 365 days after the operation and the entire graft was taken for histological analysis. In the 20 rats of Group IV, 60 days after CCA, the graft was sectioned at its center to produce wallerian degeneration of nerve fibers. 10 days after this second operation the animals were sacrificed and the nerve specimens were taken for histological study.(ABSTRACT TRUNCATED AT 250 WORDS)

Anastomosis, Surgical↗

Iron metabolism in iron-deficient male quail.

1. Male quails submitted 20 and 120 days to a low iron diet (7 ppm) were compared to female laying quails, exposed for 30 days to the same low iron regime, in order to compare the response of the iron metabolic control under a single (erythropoiesis) or a doubled (erythropoiesis and egg formation) iron demand. 2. Iron deposit in storage organs, the classical hematology and the intestinal iron absorption were analyzed in these animals. 3. In males, after 120 days, the iron deposits were reduced 50 and 75%, but hematological values (hematocrit and hemoglobin concentration) were normal, although in laying quails, after 30 days, an anemic condition was evident in both blood parameters and iron deposits, provoking an iron deficient erythropoiesis. 4. The enhancement of the intestinal iron uptake, confirms the anemic character of these birds.

Animals↗

Iron content and distribution in Japanese quail.

Determination of blood haematocrit and haemoglobin, plasma iron content, total iron binding capacity and phosphoprotein (vitellogenin), and the iron content of different organs (pectoral muscle, liver, spleen, intestine, femur bone marrow, blood, gonad and eggs, and feathers) were carried out in prelaying, onset of laying and full laying females, as well as in adult males. The whole iron content was also determined on incinerated specimens giving these results: 53.7 parts per million (p.p.m.) iron in the prelaying group, 54.5 p.p.m. iron at the onset of laying, 64.3 p.p.m. iron in full laying and 53.5 p.p.m. iron in males. The plumage represented 5-8% of the total body weight, and its iron content oscillated between 152-163 p.p.m. iron in males and non-laying females and 177.3 p.p.m. iron at full laying. The laying period induced important variations in plasma levels and in organ distribution, but not in haematological values. The first eggs laid were smaller (9.2 g) and richer in iron (427 micrograms iron) than those laid by older layers (11.8 g and 305 micrograms iron). The percentage distribution of the total iron content of organs was, in prelaying females: feathers, 21.9; blood, 56.6; pectoral muscle 8.1; liver, 9.7; intestine, 2.7. In laying females: 29.1; 46.6; 11.5; 7.4; 4.2. In males: 17.4; 59.6; 11.4; 7.9; 2.3. The increase in intestinal iron content in laying quails coincided with a double intake of food. This distribution differs from the mammalian model, as egg production (where each egg represented 2.5-5.5% of the total iron) and the great inert iron deposits in the plumage require an elaborate iron metabolism control system to cover all the iron needs in birds.

Animals↗

Os penis in a hemodialysis patient.

A case of os penis in a patient on chronic hemodialysis is described for the first time. Bilateral involvement of the corpora cavernosa was present, covered by an ossification plate.

Calcinosis↗

Iron mobilization in estrogenized male quail.

A single diethylstilbestrol (DES) injection (5 mg DES/100 g body wt) was administrated to several lots (three specimens each) of adult male quail (Coturnix coturnix japonica). The birds were sacrificed 24, 48, 72 and 96 hr after the DES injection. A significant increase in liver weight and a clear drop in the hemoglobin concentration were observed after 24 hr. Later, a progressive rise was observed in plasma iron, total iron binding capacity, plasma copper and the phosphoprotein (vitellogenin), which reached highest values after 96 hr. In the liver, the iron showed an initial increase (24 hr), due to a rise in non-ferritin iron followed by a progressive decrease. Ferritin iron increased slowly but was significantly higher after 96 hr. This experimental model on male quail suggests an estrogen response in birds that could be more general and uniform than in mammals.

Animals↗

The mass spectra of 13C labelled methylene derivatives of steroids--IV.

The mass spectra of the 3-ethylene ketal of delta 5-pregnan[20-13C]methylene-3-one and 17 beta-acetoxyl[3-13C]methyleneandrost-1-ene have been examined. In both cases there are some fragments which show either relatively large retention or elimination of 13C label and these can be assigned to some fragmentation paths which generally follow those found for diterpenic and steroidal hydrocarbons, and are in good agreement with the empirical fragmentations rules in mass spectrometry.

Carbon Isotopes↗