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M O Fernández

Publications and source records attributed to M O Fernández.

2 recordsLinked to original sources

Experimental data supporting the expression of the highly conserved GnRH-II in the brain and pituitary gland of rats.

The second GnRH form, originally identified in chickens (cGnRH-II or GnRH-II), is the most ubiquitous peptide of the GnRH neuropeptide family, being present from jawed fish to human beings. However, the presence of GnRH-II in such an important experimental model as the rat is still an object of discussion. Here we present chromatographic, immunologic and biologic activity evidence supporting the expression of GnRH-II in the rat. Olfactory bulb, hypothalamus, remnant brain and anterior pituitary from a pool of 50 female adult rats were extracted and subjected to RP-HPLC on a C-18 column. The fractions were collected and evaluated by using two different RIA systems, specific for GnRH-I and GnRH-II respectively. Under these conditions the GnRH-I standard eluted in fraction 21 (f21) was only detected with the GnRH-I RIA system, whereas the GnRH-II standard was only detected in the fraction 27 (f27) by using a GnRH-II RIA system. In the olfactory bulbs extract, the fractions analyzed by the GnRH-I RIA systems showed a single peak in f21, whereas by using the GnRH-II RIA system a single peak at f27 was observed. In the hypothalamus GnRH-I was detected in f21 meanwhile GnRH-II could not be detected. When the remnant brain and pituitary gland extracts were analyzed, both GnRH forms were detected. To the best of our knowledge, this is the first report concerning GnRH-II detection in a mammalian pituitary. Serial dilutions of f27 and GnRH-II presented similar displacement of radioiodinated-GnRH-II, demonstrating that both molecules share immunological properties. Moreover, after 60 min stimulation, both f27 and GnRH-II had similar LH and FSH releasing activity in 12 day-old rat pituitary primary cell cultures. However, we failed to characterize the GnRH-II gene in this model. These results provide strong evidence for the expression of GnRH-II in the rat brain and pituitary gland.

Animals↗

[Programming VTIM physiologic pacemakers (evoked QT)].

Seventeen VTIM pacers were implanted in seventeen patients. Average follow up were 16.7 months. This paper concerns TX track and TX on modes only. Sensing window period and slope, which determine the rate response, must be programmed carefully. Potential competitive rhythms, severe ventricular arrhythmias or inadequate rate response to physical stress may potentially develop under inadequate programming. Consequently, it is advisable to program the sensing window 20-25 ms longer than the QTE max (at LRL) and the slope at 100% of the whole value. No complications were detected. Figures 1, 2 and 3 show examples of competitive rhythms without heart stimulation and unsensed beats by abnormally long programmed SW values. When properly shortened, this interval allows proper measurement of the Stim.-T and no competitive rhythm, during almost the same spontaneous rhythm. This system fulfills the major conditions for pacing the heart: rate adaptation to neurohormonal release, to physical stress and operative mode as a close-loop system during the recovery period.

Adaptation, Physiological↗