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Prenatal development of adenohypophyseal cell types, ovary, and uterus of dromedary camel.

The somatotrophic and thyrotrophic cells were originally developed in the adenohypophysis from undifferentiated chromophobic cells at the foetal age of 4-8 weeks. The follicle-stimulating hormone cells appeared at a foetal age of 24-28 weeks. Prolactin and luteinizing hormone cells were first seen at of foetal age levels of 32-36 and 40 weeks. The germinal epithelium of flattened and cuboidal cells in the ovary was changed to cubical and columnar types, 24-28 weeks of foetal age. The sex cords appeared at 8-12 weeks of foetal age. The primary and secondary follicles were observed at 8-12 and 20-24 weeks of foetal age, respectively. Follicular cavity was noticed at 32-36 weeks, while large follicles encapsulated by follicular sheath were seen in the 40th week of foetal age. Some ovarian follicles degenerated during or after their development. Surface epithelium in the uterus changed from cubical to columnar type at 8-12 weeks of foetal age. The endometrium was clearly distinguished from the myometrium at 16-20 weeks of foetal age. The uterine glands appeared at 16-20 weeks as short and straight tubular glands, and they began to branch in the 40th week of foetal age.

Animals↗

N-terminal amino-sequencing of camel (Camelus dromedarius) luteinizing-hormone alpha and beta-subunits.

The subunits of luteinizing hormone from the Camelus dromedarius (CamLH) have been separated by reverse phase HPLC after reduction and alkylation of their disulfide bridges. The N-terminal amino-acid sequencing of the alpha and beta subunits has been performed up to the 53rd and 67th residue respectively (i.e. more than half of each polypeptide chain). These sequences have been compared to those of LH from other mammalian species in order to estimate the phylogenetic divergence of LH in this species and in order to point out characteristic features of its primary structure that can be related to its physico-chemical properties.

Amino Acid Sequence↗

Isoenzyme characterisation of 15 stocks of Trypanosoma evansi isolated from camels in the Sudan.

Fifteen stocks of T. evansi isolated in Sudan were compared using isoenzyme banding patterns. Differences between the stocks were found but overall they formed a homogeneous group. The results were similar to those obtained for other stocks of T. evansiisolated from Kenya, W. Africa, S. America and Kuwait and indicate that little genetic variation occurs in T. evansi over its geographical range. This low variation may have important implications in the development of new methods of controlling trypanosomiasis caused by T. evansi.

Alanine Transaminase↗