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Biomedical subjects

H Qi

Publications and source records attributed to H Qi.

111 records · Page 7Linked to original sources

Phenytoin-induced hyperglycaemia may confound rat cerebroprotection models.

1. The anticonvulsant phenytoin (PHT) has been used with variable success in animal models of cerebral ischaemia. Although PHT has been reported to alter glucose regulation in man, this potential effect has been largely ignored in animals. Because hyperglycaemia strongly influences the outcome of cerebral ischaemia, we sought to systematically delineate the effects of PHT on serum glucose in several rat strains. 2. We studied the PHT dose-response curve for serum PHT and glucose concentrations and several physiological variables. Phenytoin induces a significant, concentration-dependent hyperglycaemia, even in the ranges commonly used for humans and in animal models. 3. Hypothermia of several degrees was observed during PHT administration, but no hypotension or bradycardia was found. 4. Both hyperglycaemia and hypothermia must be considered when PHT is studied as a neuroprotective agent in animal models.

Animals↗

Urinary procoagulant activity and tissue factor levels in patients with diabetes mellitus.

We characterized a factor important for the normal procoagulant activity in human urine and measured urinary tissue factor (TF) and thrombomodulin (TM) levels in patients with diabetes mellitus (DM). Urine shortened normal plasma-based clotting time, which is inhibited by antibody to the human TF. TF in urine presents in membrane-nonassociated and associated forms. The urine TF antigen levels in DM patients were significantly lower than those in healthy subjects, particularly in DM patients without retinopathy. Levels of TM in patients with DM and normal subjects were similar. Although urinary TF might be necessary to repair tissue injury of damaged sites in the excretory pathway of urine, the clinical relevance of the reduced TF in the urine needs further investigation.

Blood Coagulation↗

Stability and stabilization of insulinotropin in a dextran formulation.

The stability of insulinotropin in a formulation containing 23% dextran-75 is studied. The effects of temperature, excipients, dextran concentration, and drug concentration on the stability of insulinotropin are examined. The tryptophan residue is identified as the primary degradation site in the insulinotropin molecule by LC-MS. Different antioxidants are used to stabilize the peptide. The combination of cysteine and EDTA is found to be most effective in stabilizing insulinotropin in the dextran formulation.

Buffers↗