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Biomedical subjects

H J Lin

Publications and source records attributed to H J Lin.

At least 253 records · Page 14Linked to original sources

Sitosterol and cholesterol metabolism in a patient with coexisting phytosterolemia and cholestanolemia.

Sitosterol and cholesterol metabolism were studied in a patient with coexisting phytosterolemia and cholestanolemia, and in a control subject, both on similar diets containing about 170 mg cholesterol and 135 mg phytosterols per day. The turnover of 22,23-3H-sitosterol and 4-14C-cholesterol, given intravenously, were followed for up to 372 days. The specific activity-time curves for both sterols were resolved into two exponentials and fitted into a two-pool model. The half-lives of both exponential curves for sitosterol, in the patient, were abnormally long. Equilibration of the tracer between the two pools, in the patient, occurred at about 30 days as compared to 10-15 days in the control subject. The daily turnover of sitosterol in the patient was estimated to be 10 times greater than that in the control subject. The patient's total body exchangeable pool of sitosterol was 9.6 g or about 80 times the amount found in the control. The patient's plasma phytosterol levels fell by 25% when he went on a diet containing only 10 mg phytosterols per day. During this period the specific activity of his plasma sitosterol with respect to an equilibrated dose of 3H-labeled tracer remained constant; this was compatible with the absence of endogenous synthesis. Cholesterol turnover in the patient showed prolonged half-lives for both exponential curves and reduced fractional daily loss from the fast-exchanging pool. The patient's xanthoma sterols underwent 16% and 55% exchange with plasma sitosterol and cholesterol, respectively, on day 60, indicating the presence of a third exchangeable pool.

Adult↗

Mutagenesis in Salmonella after NADH-dependent microsomal activation of dimethylnitrosamine.

The mutagenic activity of dimethylnitrosamine activated by rat-liver microsomes in the presence of NADH was compared with that obtained with NADPH. 3 histidine auxotrophic strains of Salmonella underwent reversions after activation with NADH as the sole coenzyme. All 3 tester strains showed a dose-response relationship with dimethylnitrosamine (10-125 mumoles per plate) after NADH-supported activation. With NADH as the sole coenzyme, the most sensitive strain, hisG46, showed a 105-fold increase in mutagenesis frequency as compared with the 230-fold increase obtained with NADPH. Activation of dimethylnitrosamine in the presence of NADH and NADPH, in combination, produced mutagenesis at frequencies above those seen with NADH alone, but less than or equal to those seen with NADPH as the only coenzyme during the activation step. Experiments in vitro showed that microsomal incorporation of carbon from [14C]dimethylnitrosamine was highest in the presence of NADPH, lowest with NADH and reached intermediate levels when both coenzymes were present. The source of the microsomes in all experiments was liver from rats pre-treated with Aroclor 1254.

Animals↗

The reassociation curve of human DNA amended.

The reassociation kinetics of human DNA was studied, utilizing S1 nuclease digestion in aqueous dioxane and hydroxyapatite chromatography for isolating renatured DNA. The percentage of DNA reassociated at C0t = 10(-3) was 5--7% and that at C0t = 18 000 was about 85%, C0t being the product of the molar concentration of DNA and the reassociation period in s. The shape of the amended reassociation curve was roughly that of a rectangular hyperbola. It showed pronounced differences from the curves obtained by direct hydroxyapatite chromatography of reassociated DNA. The S1 nuclease-dioxane procedure offered two advantages over the conventional method. It was applicable to the study of reassociation with high molecular weight DNA, and the reassociated DNA so obtained was devoid of low-melting strands. The analysis of the new data took into account the possible effects of the diploid condition on the reassociation rate of DNA, the source of the DNA used in this study being placental tissue. The new reassociation profile was compared to ideal second-order reassociation curves calculated for the human genome (2.5 . 10(9) nucleotide pairs), and for a genome twice this size, containing various proportions of single-copy sequences. The results showed that approximately 85--90% of th total DNA may consist of unique sequences. This estimate is considerably higher than those reported previously.

DNA↗

A unique patient with coexisting cerebrotendinous xanthomatosis and beta-sitosterolemia.

An adult Chinese man presented with tendinous and tuberous xanthomatosis and severe atheromatous changes in the coronary arteries. In addition, he had chronic hemolytic anemia, with spherostomatocytic erythrocytes. Cerebrotendinous xanthomatosis was diagnosed on the basis of increased cholestanol levels in his plasma, red cells and xanthoma, changes in bile acid composition due to the defective synthesis of chenodeoxycholic acid. Coexisting beta-sitosterolemia was confirmed by the finding of large amounts of the plant sterols such as beta-sitosterol and campesterol. This is the first report of these two rare lipid storage disorders in the same patient.

Adult↗

Absence of the ether lipid tumour marker in diethylnitrosamine-induced rat liver cell cancer.

Tissue levels of neutral O-alkylglycerolipids were measured in rat liver during the course of hepatocarcinogenesis produced by feeding diethylnitrosamine. Enzyme altered foci, not recognizable with conventional histological techniques, were shown to be present in specimens obtained after 3 or 6 weeks feeding the carcinogen. Frank hyperplastic nodules were present at 11 weeks and hepatocellular carcinoma were found in all rats at 18 weeks. At no point during the course of carcinogenesis did the liver show an increase in either-linked neutral glycerolipids, characteristic of animal tumours. On the contrary, lower levels of neutral O-alkylglycerolipids were found in tissues containing hyperplastic nodules or tumour.

Animals↗

Development of new mitomycin C and porfiromycin analogues.

New mitomycin C and porfiromycin analogues were prepared by treating mitomycin A and N-methylmitomycin A with a variety of amines, including aziridines, allylamines, propargylamines, chloroalkylamines, hydroxyalkylamines, glycine derivatives, aralkylamines, and heterocyclic amines. All analogues were evaluated against P-388 murine leukemia and selected ones were examined for their leukopenic properties. Certain analogues were found to be superior to mitomycin C in potency, efficacy, and therapeutic ratio in the P-388 assay. The most active substituents at the mitosane 7 position included aziridine, 2-methylaziridine, propargylamine, furfurylamine, methyl glycinate, and 3-aminopyridine. Mitomycin A and the 7-aziridino, 7-(2-methylaziridino), and 3-aminopyridine analogues were less leukopenic than mitomycin C. Certain other analogues, including propargylamino and methyl glycinate, were highly leukopenic. The three compounds tested against B-16 melanoma in mice were significantly more effective than mitomycin C in this assay. Previously established structure--activity relationships were found inadequate to account for all of the new data.

Animals↗

Methylation of DNA in target and non-target organs of the rat with methylbenzylnitrosamine and dimethylnitrosamine.

The sites of labelling of DNA with [14C]methyl groups from methylbenzylnitrosamine and dimethylnitrosamine were studied in rat oesophageal epithelium and liver. All four combinations of tissue and carcinogen were studied. Tissues were labelled in vitro and the DNA contained therein purified and hydrolysed (pH 1, 37 degrees C) to free purines and apurinic acid. Quantitative analysis was performed with the aid of thin-layer chromatography. The apurinic acid and 7-methylguanine fractions were found to be extensively labelled. Smaller amounts of radioactivity were found in O6-methylguanine and some of the methylated adenines. The same carcinogen produced different patterns of labelling is oesophageal and liver DNA. The proportion of O6-methylguanine to 7-methylguanine was higher when the methylating agent was a carcinogen specific for the organ.

Animals↗