Search PubMed⌕ Search

Biomedical subjects

M Ujhelyi

Publications and source records attributed to M Ujhelyi.

8 recordsLinked to original sources
PubMed2000

Observations on the behavior of gibbons (Hylobates leucogenys, H. gabriellae, and H. lar) in the presence of mirrors.

Three captive gibbons (Hylobates leucogenys, H. gabriellae, and H. lar) were videotaped in the course of longitudinal exposure to mirrors introduced into their familiar cage or island housing situation. The gibbons, which differed in age, sex, species, and rearing condition, exhibited great individual differences in their behavioral reactions to mirrors, spanning from a minimal reaction dominated by social responses to a dramatic sequence of progressive behavioral change that featured a variety of contingency testing behaviors and included mirror-mediated, self-directed behavior. Additional information on the mirror competence of gibbons was provided by modified mark tests and a hidden object task. The results are discussed in relation to current criteria for self-recognition in primates and factors involved in individual and species differences in reactions to mirror exposure.

Animals↗
PubMed1996

Is there any intermediate stage between animal communication and language?

Animal communication and human language have fundamental differences in their structures and functions. Furthermore, there is no living species demonstrating an intermediate stage of language evolution. Thus, we have difficulty in finding characteristics attributable to a communication system which can already be considered as a starting point for linguistic evolution. However, some findings coming from neurolinguistic research give us the opportunity to suppose that varying and arranging linguistic elements can be detached from other grammatical functions. Further information in this direction comes from apes' language-teaching experiments; namely bonobos (Pan paniscus) are able to understand and produce differences in meaning by varying word arrangements. Based on these results one can suppose that an acoustic signal system, which possesses discrete units for variable use, might be very ancient and might exist independent and prior to a more advanced language state. In the natural setting, acoustic territorial marking behaviour is exposed to selection pressure to elaborate sign systems built up from discrete, variable units. In addition to the well-known territorial bird songs, some monkey species and all species of lesser apes have territorial songs fitting these criteria. The analyses of the so-called long calls in chimpanzees and bonobos make it likely that the group-living great apes preserved the ability to create syntactically different calls, which would be developed by requirements of social life. A call repertoire emerged in these species, which contained a large number of call variants at group level available for each group member via social learning. This type of animal call is different from ordinary animal communication; it shows some features of human language. It can represent an intermediate stage between animal communication and language, and communication systems similar to this one can be considered as a starting point or first stage of language evolution.

Animal Communication↗
PubMed1996

Antagonistic properties of centrally truncated analogs of [D-Trp(32)]NPY.

We have previously shown that [D-Trp(32)]NPY can competitively antagonize NPY-induced feeding in rats (Balasubramaniam et al. J. Med. Chem. 1994, 37, 811-815). This peptide, however, did not bind to SK-N-MC cells with Y-1 receptors. Since centrally truncated NPY analogs have been shown to bind Y-1 receptors, we synthesized similar analogs of [D-Trp(32)]NPY and investigated their Y-1 (SK-N-MC) and Y-2 (SK-N-BE2) receptor affinities and their properties in human erythroleukemia (HEL) cells. None of the analogs with D-Trp(32) mobilized intracellular calcium, [Ca2]i, in HEL cells. Although Des-AA(6-24)[Aoc(6)]NPY and the corresponding D-Trp(32) analog exhibited no affinity to Y-1 receptors, Des-AA(7-24)[Aoc(6),D-Trp(32)] NPY(6) exhibited weak binding. Replacing Pro(5) in 6 with D-Ala to stabilize the central chain reversal, and hence the antiparallel alignment of the N- and C-terminal regions known to be important for Y-1 binding, resulted in an analog, Des-AA(7-24)[D-Ala(5),Aoc(6),D-Trp(32)]NPY (7), which exhibited moderate antagonist potency in attenuating NPY effects on cAMP and [Ca2+]i, in SK-N-MC and HEL cells, respectively. This analog also shifted the dose-response curve of NPY on blood pressure in anesthetized rats. Deletion of only the 7-17 and/or the incorporation of N-Me-Ala(5), superior beta-turn stabilizer, in 7 did not improve the Y-1 receptor affinity. Des-AA(7-24)[D-Ala(5), Gly(6),D-Trp(32)]NPY exhibited an affinity similar to that of 7, suggesting that a long spacer arm is not necessary for efficient Y-1 receptor interaction. Locking the antiparallel alignment via a 2/26 or 2/27 lactam bridge did not improve the binding. Finally, replacement of D-Ala(5) in 7 with D-Trp dramatically increased both the binding and the antagonistic potencies. Modeling based on the avian pancreatic polypeptide X-ray structure suggested that analogs which have the N- and C-terminal regions in close proximity might exhibit good binding, and that the D-Trp(32) substitution may induce a beta-turn that could be important for exhibiting antagonism. A systematic investigation has resulted in the development of relatively potent Y-1 receptor antagonists. Further structure-activity studies with these compounds and those previously reported by us and other investigators should result in the development of long-acting and receptor selective antagonists.

Amino Acid Sequence↗
PubMed1995

High-performance liquid chromatographic analysis of pindolol enantiomers in human serum and urine using a reversed-phase cellulose-based chiral column.

Simple, sensitive and reliable high-performance liquid chromatographic methods are reported for the determination of pindolol enantiomers in human serum and urine. The methods involved a solid-phase extraction of serum and a direct injection of urine samples. The separation of R(+)- and S(-)-pindolol was accomplished on a reversed-phase cellulose-based chiral column with a mobile phase of 40:60 (v/v) acetonitrile-0.3 M aqueous sodium perchlorate at a flow-rate of 0.5 ml/min. The detection was achieved by monitoring the fluorescence emission of pindolol enantiomers at 310 nm with excitation at 270 nm. The limits of detection were 1.2 ng/ml of R(+)- and 4.3 ng/ml of S(-)-pindolol in serum, and 21 ng/ml of R(+)- and 76 ng/ml of S(-)-pindolol in urine. The external standard method was used for quantitation. The methods have been applied to the analysis of human serum and urine samples in a pharmacokinetic study.

Adrenergic beta-Antagonists↗
PubMed1995

Lidocaine prophylaxis for fatal ventricular arrhythmias after acute myocardial infarction.

OBJECTIVE: To compare the efficacy and safety of a 40-hour lidocaine infusion after completion of a 8-hour open-label infusion for prophylaxis of primary ventricular fibrillation in patients with uncomplicated acute myocardial infarction. METHODS: This was a double-blind, randomized placebo-controlled trial held in the coronary care unit of a large nonprofit hospital. We studied 200 patients with uncomplicated acute myocardial infarction in Killip class I or II who came to the hospital within 6 hours of onset of symptoms and 22 patients who had ventricular fibrillation before the start of the study. Intervention consisted of an 8-hour lidocaine infusion followed by placebo or lidocaine for an additional 40 hours. The infusion rate was adjusted in patients > or = 70 years old and in those < 50 kg or > or = 90 kg. Measurements recorded were baseline demographic characteristics, incidence of ventricular arrhythmias, adverse reactions, and death. RESULTS: New congestive heart failure developed during the randomized phase in 9% of patients receiving lidocaine and in 2% of patients receiving placebo (p = 0.03). Ventricular fibrillation did not occur during the treatment period, and sustained ventricular tachycardia developed in one patient receiving placebo. The in-hospital mortality rate was comparable in both groups (4% versus 2%; p = 0.68) but was much higher (13.6%) in patients with initial ventricular fibrillation not included in the randomized study. CONCLUSIONS: A 40-hour age- and weight-adjusted lidocaine infusion administered after an initial 8-hour infusion provoked more congestive heart failure than placebo. In view of the absence of ventricular fibrillation episodes with both infusions, caution should be used when lidocaine is administered for longer than 8 hours in patients with uncomplicated myocardial infarction.

Aged↗
PubMedDate not supplied

The possible common origin of tRNA and 5S rRNA.

Seryl tRNA (anticodon GCU) from mammalian mitochondria shows in comparison to other mitochondrial tRNAs additional special features differing from the generalized tRNA model. When arranged in the traditional cloverleaf form, eight bases fall within the T psi C loop, and the entire dihydrouridine loop is lacking. This seryl tRNA molecule is therefore shorter than other tRNAs. It was originally thought to represent a mitochondrial analog of 5S rRNA and its precise classification is still disputed. The present studies suggest that this mitochondrial tRNA represents a fossil molecule which is related to the common ancestor of the present tRNA and 5S rRNA molecules.

Animals↗