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Biomedical subjects

R Maier

Publications and source records attributed to R Maier.

At least 145 records · Page 8Linked to original sources
PubMed1975

Effects of various hypolipidemic drugs on fatty acid composition of liver and serum lipids.

1. Treatment of rats with hypolipidemic drugs elicited an increase in oleic and a decrease in linoleic acid content in cholesterol esters, triglycerides and phospholipids of serum and liver lipids. 2. The change was most pronounced in triglycerides followed by cholesterol esters and phospholipids. 3. The shift was dose-dependent, starting with doses eliciting hypolipidemic effects. 4. The shift became obvious immediately after beginning of treatment and reached after 4 days a new steady state. 5. This effect was shared by both drugs of aryloxy fatty acid structure, but was not seen with either L-thyroxine or nicotinic acid. 6. The mechanism underlying this phenomenon is thus far unknown, but in our view it merits further attention.

Animals↗
PubMed1975

Analogues of human calcitonin. II. Influence of modifications in amino acid positions 1, 8 and 22 on hypocalcemic activity in the rat.

The calcitonin analogues [Val8] -HCT and [Tyr22] -HCT, each with a single modification, and [Val8, Tyr22] -HCT and [Bmp1, Val8] -HCT, with two replaced amino acids were compared with synthetic human calcitonin (HCT) in respect of their hypocalcemic effects in the rat. The introduction of either valine in place of methionine in position 8 or of tyrosine for phenylalanine in position 22 of the HCT molecule yielded analogues 4 to 5 times as potent and nearly twice as long-acting as HCT. The doubly substituted peptide [Val8, Tyr22] -HCT displayed properties closely similar to those of [Val8] -HCT and [Tyr22] -HCT. The analgoue [Bmp1, Val8] -HCT, with a deaminated cysteine residue at the N-terminus, was about 6 times more potent than HCT and slightly longer-acting than [Val8] -HCT.

Animals↗