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1.
J Diabetes Investig ; 13(11): 1943-1944, 2022 Nov.
Article in English | MEDLINE | ID: mdl-35620974

ABSTRACT

We showed a case with the onset of fulminant type 1 diabetes mellitus (FT1DM) whose HbA1c could not be measured with HPLC method. We think that the reason why his HbA1c was not be detected was associated with the presence of labile hemoglobin A1c (LHbA1c). These result mean that it is possible that LHbA1c can bring about a pitfall on HPLC method in diagnosis of onset of FT1DM.


Subject(s)
Diabetes Mellitus, Type 1 , Humans , Diabetes Mellitus, Type 1/diagnosis , Chromatography, High Pressure Liquid , Glycated Hemoglobin/analysis , Diagnosis, Differential
2.
J Pharm Pharmacol ; 55(10): 1419-26, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14607025

ABSTRACT

As the consumption of herbal remedies has increased, the opportunity that such herbal medicines are co-administered with other drugs has also risen gradually and we are, therefore, very much concerned about herb-drug interactions. We examined the effects of pre-administration of Kampo medicines (Sho-saiko-to, Saiko-keishi-to, Shigyaku-san and Dai-saiko-to) on the pentobarbital-induced sleeping time in mice and rats, to clarify the possibility that they could affect the drug-metabolizing enzymes. The administration of Sho-saiko-to and Saiko-keishi-to for 4 weeks significantly shortened the pentobarbital-induced sleeping time in mice and the administration of Sho-saiko-to for 2 weeks significantly reduced the sleeping time in rats. Furthermore, we tried to identify the molecular species of rat cytochrome P450s (CYPs) affected by Sho-saiko-to and Saiko-keishi-to by competitive RT-PCR. The oral administration of Sho-saiko-to for 2 weeks upregulated the mRNA expression of CYP2B, CYP3A1, CYP2E1 and CYP4A1 in rats. The treatment with Saiko-keishi-to for 2 weeks also up-regulated the mRNA expression of CYP2B, CYP3A1 and CYP4A1. Sho-saiko-to and Saiko-keishi-to may potentially influence the drug-metabolizing enzymes in man, and would thus require much attention when used in the clinical situation.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Cytochrome P-450 Enzyme System/drug effects , Drugs, Chinese Herbal/adverse effects , Animals , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Cytochrome P-450 Enzyme System/biosynthesis , Drug Administration Schedule , Drug Interactions , Drugs, Chinese Herbal/administration & dosage , Female , Hypnotics and Sedatives/pharmacokinetics , Hypnotics and Sedatives/pharmacology , Mice , Mice, Inbred ICR , Phenobarbital/pharmacokinetics , Phenobarbital/pharmacology , RNA, Messenger/analysis , Rats , Reverse Transcriptase Polymerase Chain Reaction , Sleep/drug effects , Up-Regulation
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