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M T Alsalami

Publications and source records attributed to M T Alsalami.

3 recordsLinked to original sources

Haematology of foetal sheep.

OBJECTIVE: To describe the ontogeny of blood cells throughout foetal development in sheep. DESIGN: A haematological study on blood and bone marrow from 42 sheep foetuses aged between 19 days gestation and full term. PROCEDURE: Virgin Merino ewes were mated and the developing foetuses removed surgically at different stages of gestation. Blood and bone marrow samples were collected, stained for cytological examination or processed for electron microscopy. Blood samples were also examined haematologically. Foetuses were incubated with 3H-thymidine and autoradiographed. RESULTS: During the first 4 weeks of development primitive erythroblast constituted the majority of the circulating blood cells. Definitive erythroid cells, originating in the liver, first appeared in the blood at around 27 days gestation and entirely replaced the primitive erythroblasts by 50 days gestation. Leukocyte numbers, especially lymphocyte count, increased rapidly after 49 days gestation. Erythropoiesis predominated in the marrow of all foetuses older than 70 days. In more marrow, myelopoiesis was the major activity and lymphopoiesis was not significant. CONCLUSIONS: Red blood cell numbers and haemoglobin content progressively increases during foetal development. Primitive erythroblasts are not the precursors of the definitive erythroblasts. There are no significant differences in morphological features or maturation sequence between hepatic and bone marrow erythroblasts. Myelopoiesis is a major activity of bone marrow rather than of foetal liver.

Animals↗

Hepatotoxic and nephrotoxic principles in Terminalia oblongata.

A study was conducted to identify and characterise the toxic principle in Terminalia oblongata, commonly known as yellow-wood. Crude aqueous extracts of yellow-wood leaf were found to produce the same liver lesion in mice as has been reported in ruminants. The hepatotoxic fraction was isolated and identified as a hydrolysable vegetable tannin called punicalagin. When given orally, the dose required to produce toxicity was at least 20 times greater than when given intraperitoneally. Following a given dose of punicalagin, the onset and severity of liver necrosis was found to be related to the time interval after dosing. In addition to punicalagin, an unidentified nephrotoxic substance was found which was capable of producing avascular renal necrosis without liver necrosis.

Administration, Oral↗