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M Rathbone

Publications and source records attributed to M Rathbone.

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Suppression of ovarian progesterone production in dairy cows using an implant of GnRH-agonist (deslorelin) for the purpose of evaluating progesterone metabolism [corrected].

OBJECTIVE: To evaluate the potential of an implant of a GnRH-agonist (deslorelin) to create a progesterone free animal suitable for studying progesterone (P4) metabolism in intact cows by measuring blood P4 and faecal P4 metabolites. METHODS: Experiment 1: Eighteen non-lactating cycling Holstein-Friesian cows, 4 to 7 years old, were allocated to one of three groups to study plasma P4 concentrations preceding an intravaginal insert. These groups comprised: i) a deslorelin group (GnRH-agonist implanted); ii) a PGF group receiving two injections of prostaglandin (PGF2alpha) 12 days apart; and, iii) an ovariectomised (OVX) group. An intravaginal device (CIDR) was inserted into the vagina of each animal and left in place for 11 days. Plasma P4 concentrations were measured during the study period. Experiment 2: Twelve non-lactating cycling Holstein-Friesian cows, 4 to 7 years old, were allocated to two groups: i) a deslorelin group (GnRH-agonist implanted); and ii) an ovariectomised group. Plasma P4 and faecal P4 metabolites (20-oxo-pregnanes, 20alpha-OH and 20beta-OH) were monitored for a period of 5 weeks. RESULTS: Experiment 1: Average plasma P4 concentration did not differ between the three groups (1.28, 1.43 and 1.55 ng/mL for deslorelin, OVX and PGF cows, respectively, P = 0.8) during the period of supplementation. Experiment 2: There was no difference in plasma P4 (mean plasma P4 < 0.02 ng/mL, P = 0.9) and faecal P4 metabolites between deslorelin and OVX cows 2 weeks after the implantation (P = 0.7). CONCLUSIONS: These data showed that a GnRH-agonist (deslorelin) implant may be used as an alternative to ovariectomy to create a progesterone free animal suitable for studying the metabolism of administered P4.

Administration, Intravaginal↗

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Purification of a chick brain-derived growth factor by reversed-phase high-performance liquid chromatography.

A chick brain-derived growth factor (CBGF) has been purified to apparent homogeneity by a combination of ultrafiltration, DEAE ion-exchange, and reversed-phase high-performance liquid chromatography on a C18 column. CBGF has an apparent molecular mass of approximately 1500 Da. The amino acid composition of CBGF has been determined and reveals a peptide containing predominantly glycine, glutamic acid/glutamine, and aspartic acid/asparagine. This mitogen is highly active, with half-maximal stimulation of chick brain astrocytes at 5 ng/ml in an assay using incorporation of methyl-3H-thymidine into DNA. In addition to its effects on chick astrocytes, purified CBGF from the 18 d chick embryo is mitogenic for amphibian limb regeneration blastema cells in vitro. A possible role for this mitogen in the nerve-dependent regeneration of amphibian appendages is discussed.

Animals↗