Neuroendocrine hypothalamus as a homeostat of endogenous time

The concept of the hypothalamus as a brain structure responsible for metabolic and thermal homeostasis of an organism emerged in the 60s and 70s of the XX century (hypothalamus as a homeostatic or thermal homeostat). In the following decades, studies of molecular mechanisms behind the genesis of circadian and circannual rhythms sinificantly expanded our knowledge of hypothalamic functions. According to current ideas, hypothalamic nuclei function as pacemakers for other structures and trigger various processes that have different temporal parameters (latency, velocity, duration, periodicity, sequentiality, density) and form together the organism’s endogenous time. In this review, the authors analyze some features of local networks in the hypothalamic nuclei and formulate the principles of neuropeptide action underlying the homeostatic regulation of the endogenous time by the hypothalamus.     

The parkinsonism producing neurotoxin MPP+ affects microtubule dynamics by acting as a destabilising factor

Dysfunction of the microtubule system is emerging as a contributing factor in a number of neurodegenerative diseases. Looking for the potential role played by the microtubule cytoskeleton in neuron degeneration underlying Parkinson's disease (PD), we investigate the influence of the parkinsonism producing neurotoxin 1-methyl-4-phenylpyridinium (MPP+) on microtubule dynamics. We find that it acts as a strong catastrophe promoter causing a decrease of the average length of microtubules assembled from purified tubulin. We also find that it reduces the number of microtubules nucleated from purified centrosomes. Finally, binding assays demonstrate that the neurotoxin binds specifically to tubulin in the microtubule lattice in a close to stoichiometric manner. This paper provides the first evidence that dynamic instability of microtubules is specifically affected by MPP+ and suggests that it could play a role in neuronal cell death underlying PD.     

Human NCU-G1 can function as a transcription factor and as a nuclear receptor co-activator

Background  

Novel, uncharacterised proteins represent a challenge in biochemistry and molecular biology. In this report we present an initial functional characterization of human kidney predominant protein, NCU-G1.