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E Shen

Publications and source records attributed to E Shen.

At least 37 records · Page 2Linked to original sources
PubMed1991

Respiratory neurons in the medulla of the rabbit: distribution, discharge patterns and spinal projections.

To determine distribution, discharge patterns and the spinal projections of medullary respiratory neurons (RNs), a systematic mapping of 806 RNs was made in the medulla of anesthetized rabbits. In disagreement with previous reports that there are no discrete medullary respiratory neuronal groups in rabbits, two neuronal groups were identified: (1) dorsal respiratory group (DRG), associated with the nucleus tractus solitarius; and (2) ventral respiratory group (VRG), associated with the nucleus ambiguus compact formation. The density of RNs in the DRG was much lower than that in the VRG. In the VRG, 3 subdivisions of RN populations were found: predominantly expiratory neurons in the caudal and the rostral parts, and mainly inspiratory neurons in the intermediate region. Nine distinct types of RNs were classified on the basis of firing patterns. Nearly all types were found in both the DRG and each VRG subdivision. Antidromic mapping of 64 VRG neurons revealed that 67% projected to the spinal cord. Expiratory bulbospinal neurons in the rostral subdivision of the VRG projected only to the cervical cord (mainly ipsilaterally). Most neurons of the intermediate and caudal subdivisions of the VRG (74%) appeared to project either contralaterally or ipsilaterally below T. The axonal conduction velocity was 40-50 m/s by two-point determinations. We conclude that respiratory neuronal groups in the medulla of the rabbit are generally similar to those of the cat. Nearly equal proportions of bulbospinal RNs projected to the ipsilateral vs contralateral spinal cord.

Anesthesia↗
PubMed1991

Excitatory postsynaptic potentials evoked by ventral root stimulation in neonate rat motoneurons in vitro.

1. Intracellular recordings were made from antidromically identified motoneurons in transverse (500 microns) lumbar spinal cord slices of neonatal (12-20 day) rats. 2. Electrical stimulation of ventral rootlets evoked, with or without an antidromic spike or initial segment potential, a depolarizing response (latency, 1-4.2 ms), a hyperpolarizing response (latency, 1.5-3.5 ms), or a combination of two preceding responses in 38, 6, and 8% of motoneurons investigated. 3. The hyperpolarizing response was reversibly eliminated by low Ca2+ (0.25 mM), d-tubocurarine (d-Tc; 10 microM) or strychnine (1 microM), suggesting that this response represents an inhibitory post-synaptic potential (IPSP) mediated by glycine or a related substance release from inhibitory interneurons subsequent to their activation by axon collaterals in a manner analogous to the Renshaw cell circuitry described for the cat motoneurons. 4. The depolarizing responses were excitatory postsynaptic potentials (EPSPs), because they could be graded by varying the stimulus intensity and were reversibly abolished in low Ca2+ solution. 5. Membrane hyperpolarization increased the amplitude of EPSPs, and the mean extrapolated reversal potential was -4 mV. 6. EPSPs were augmented, rather than diminished, by dihydro-beta-erythroidine (1 microM) or d-Tc, arguing against a role of recurrent motor axon collaterals in initiating the responses. 7. The conduction velocity of the fibers initiating the EPSPs ranged from 0.35 to 0.96 m/s, indicating that these fibers were unmyelinated. Furthermore, the EPSP exhibited a constant delay when the stimulus frequency was varied from 1 to 5 Hz, and the synaptic delay estimated by extrapolation was less than 1 ms, suggesting that it was a monosynaptic event. 8. After complete separation of the ventral and dorsal horns by a knife cut, stimulation of ventral rootlets could still evoke an EPSP in motoneurons. 9. Superfusion of the slices with the nonselective glutamate receptor antagonist kynurenic acid (0.2-1 mM) or the selective quisqualate/kainate receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (DNQX) (0.5-1 microM) reversibly diminished the EPSPs. 10. EPSPs evoked by stimulation of dorsal and ventral rootlets exhibited different latency and waveform in the same motoneurons. 11. The results provide evidence that activation of ventral root afferents evoked an EPSP mediated by glutamate or a related substance in a population of motoneurons. Furthermore, the afferent pathway mediating the EPSP appears to be monosynaptic and confined to the ventral horn.

Action Potentials↗
PubMed1990

Excitatory and inhibitory transmission from dorsal root afferents to neonate rat motoneurons in vitro.

Intracellular recordings were made from antidromically identified motoneurons in neonate (12-22 days) rat transverse spinal cord slices and the transmitters and receptors probably involved in initiating the excitatory (EPSP) and inhibitory (IPSP) postsynaptic potentials were investigated. Stimulation of dorsal roots elicited in motoneurons an EPSP, an IPSP, or an EPSP followed by an IPSP. EPSPs in 70% of motoneurons had a short latency (less than or equal to 1 ms) and in the remaining cells a latency longer than 1 ms. The IPSPs had a long latency (greater than or equal to 1 ms). Short- and long-latency EPSPs were enhanced by the acidic amino acid uptake inhibitor L-aspartic acid-beta-hydroxamate (AAH) and depressed by the non-selective glutamate receptor antagonists gamma-D-glutamylglycine (DGG) and kynurenic acid. Short-latency EPSPs were suppressed by the quisqualate/kainate (QA/KA) receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (DNQX) but not by the N-methyl-D-aspartate (NMDA) receptor antagonists D-(-)-2-amino-5-phosphonovaleric acid (APV) and ketamine. Long-latency EPSPs were reduced by DNQX as well as by APV and ketamine. Superfusion of the slices with a Mg-free solution increased the EPSPs and unmasked a late, APV-sensitive component. The IPSP was reduced by the glycine antagonist strychnine as well as by APV and ketamine but resistant to DNQX. The results indicate that stimulation of dorsal roots elicited in motoneurons a monosynaptic EPSP mediated by glutamate/aspartate acting predominantly on the QA/KA subtype of glutamate receptors; an NMDA component can be unveiled in Mg-free solution.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗
PubMed1990

Neonate rat sympathetic preganglionic neurons intracellularly labelled with lucifer yellow in thin spinal cord slices.

Sympathetic preganglionic neurons and interneurons were intracellularly labelled with lucifer yellow in thin transverse spinal cord slices of neonatal rats. Preganglionic neurons had spindle or oval shape somata and were located in the intermediolateral nucleus. The axons of these neurons coursed ventrally along the border of gray matter and exited the ventral horn; two to four long dendrites projected medially to the central canal and several relatively short dendrites oriented toward the lateral white matter. Interneurons were generally multipolar and located outside the immediate area of intermediolateral nucleus; their axons could sometimes be traced to the ventral funiculus. Interestingly, dye-coupled preganglionic neurons were observed for the first time. Our findings suggest that the dendritic domain of neonatal rat sympathetic preganglionic neurons is out-reaching and may represent potential sites of interaction with incoming segmental and/or descending inputs. In addition, the observation of dye-coupled preganglionic neurons raises the possibility that these neurons may have the capability of recruiting and/or synchronizing sympathetic outflow.

Adrenergic Fibers↗
PubMed1990

APV-sensitive dorsal root afferent transmission to neonate rat sympathetic preganglionic neurons in vitro.

1. Intracellular recordings were made from antidromically identified sympathetic preganglionic neurons (SPNs) in transverse thoracolumbar spinal cord slices from neonate (12- to 22-day-old) rats. 2. Electrical stimulation of dorsal roots or dorsal root entry zone elicited in SPNs an excitatory postsynaptic potential (EPSP) or multiple EPSPs of varying latencies. The EPSP could be graded by varying the stimulus intensity and, on reaching the threshold, discharged an action potential. 3. The dorsal root-evoked EPSPs had a mean synaptic latency of 2.6 ms (range: 1.2-11 ms), suggesting a polysynaptic pathway. The EPSPs were characteristically slow in onset with a mean rise time and half-decay time of 8.3 and 23 ms, respectively. 4. At the resting membrane potential of -50 to -60 mV, the amplitude of EPSPs recorded in normal (1.3 mM Mg2+) Krebs solution was reduced by membrane hyperpolarization or depolarization. In Mg2(+)-free solution, EPSPs were potentiated and reached threshold for spike discharge. 5. The EPSPs were suppressed by the nonselective glutamate receptor antagonist kynurenic acid (0.1-0.5 mM) and by the N-methyl-D-aspartate (NMDA) receptor antagonists D-2-amino-5-phosphonovaleric acid (APV; 1-10 microM) and ketamine (5-10 microM), but not by the quisqualate (QA)/kainate (KA) receptor antagonist 6,7-dinitroquinoxaline-2,3-dione (DNQX, 1-10 microM). The latter depressed the EPSPs elicited by stimulation of lateral funiculus in the same SPNs. 6. NMDA applied by pressure elicited a depolarization in the SPNs. In normal Krebs solution the response was voltage dependent with the peak amplitude occurring around -60 mV; conditioning depolarization or hyperpolarization diminished the response.(ABSTRACT TRUNCATED AT 250 WORDS)

2-Amino-5-phosphonovalerate↗
PubMed1987

Antidromic mapping of descending axons of respiratory bulbospinal neurons in the nucleus tractus solitarius of the rabbit.

Antidromic mapping of the descending axons of the respiratory bulbospinal neurons in the region of the nucleus tractus solitarius (NTS) was performed on rabbits anesthetized with urethane. Among 177 units tested, 29 out of 87 inspiratory (I), 27 out of 84 expiratory (E) and 2 out of 6 phase-spanning units were identified as bulbospinal. A prominent feature of the bulbospinal pathway from the NTS in the rabbit is the abundance of ipsilateral descending axons. The axons rising from one side are situated in the ventrolateral and ventral funiculi of both sides. The axonal conduction velocities are about 25-35 m/s. Both I and E bulbospinal neurons can be divided into R alpha and R beta types according to 'no I inflation' and 'maintained E inflation' tests.

Animals↗
PubMed1987

Cryopreservation of mouse 2-cell embryos and ova by vitrification: methodologic studies.

Cryopreservation of unfertilized mouse ova and 2-cell embryos by a vitrification technique was examined. Survival was defined by development to the hatching blastocyst stage after in vitro fertilization. With 19 embryos at the 2-cell stage, the authors obtained 100% morphologic survival and 89% development to hatching blastocyst stage. To define the optimal conditions for vitrification of ova, the authors treated a total of 845 unfertilized ova. In experiments done at 0 degree C, the concentration of vitrification solution (VS1) and the length of exposure of ova to VS1 both had significant (P less than 0.01) effects on survival. The mean survival rate for controls in ten experiments was 52%. VS1 100% or 90% in HEPES buffered saline and 10 minutes' exposure yielded rates that did not differ significantly from controls. Significantly lower survival rates followed the use of 70 and 80% solution and exposure for 5, 15, 20, or 30 minutes. Thus, under these conditions, exposure of unfertilized mouse ova to VS1 and cooling to 0 degree C did not interfere with in vitro fertilization and development of embryos. However, in five experiments in which a total of 101 ova were plunged into liquid nitrogen after treatment with VS1 under the optimal conditions, none could be fertilized in vitro.

Animals↗
PubMed1987

Hemodynamic and electrophysiologic effects of encainide in patients with bundle branch block.

Electrophysiologic studies were performed in 6 consecutive patients with bundle branch block and organic heart disease. All were studied after intravenous (0.9 mg/kg) encainide and 3 of the 6 after 36-72 hours of oral encainide (50 mg every 6 hours). After intravenous encainide, mean H-Q increased from 51 +/- 20 msec to 58 +/- 25 msec (14% p less than or equal to .05). After oral encainide (3 patients) H-Q increased to 90 +/- 39 msec (56% p less than or equal to .05, compared to baseline). Programmed ventricular stimulation was performed in 5. In 1 patient without spontaneous ventricular tachycardia, tachycardia was non-inducible before and after encainide. Of 5 patients with spontaneous arrhythmia, 3 had ventricular tachycardia induced before and after intravenous encainide at mean cycle lengths of 287 +/- 130 msec and 407 +/- 261 msec, (not significant) respectively, while 1 had ventricular tachycardia induced only after encainide. Four patients began chronic treatment with oral encainide (2 patients with inducible rapid ventricular tachycardia after encainide were excluded). All suffered major adverse outcomes. One died suddenly after an electrophysiology study demonstrated inducible ventricular tachycardia, which occurred only after encainide. One experienced new syncope after baseline H-Q increased 75% after encainide. Two patients developed new sustained atrial tachycardias and 1 patient developed persistent ventricular tachycardia on encainide.(ABSTRACT TRUNCATED AT 250 WORDS)

Administration, Oral↗
PubMed1986

Respiration related neurons in the region of the nucleus tractus solitarius of the rabbit.

Systematic mapping of respiration-related units (RRUs) in the region of the nucleus tractus solitarius (NTS) was performed on rabbits anesthetized with urethane. Of 523 RRUs 295 (56%) were inspiratory (I), 130 (25%) expiratory (E) and 98 (19%) phase-spanning (PS). Such a large number of E and PS RRUs in NTS have not been reported in the cat. Six out of 16 I RRUs 6 of 13 E RRUs, and 1 of 3 PS RRUs had projections to contralateral cervical spinal cord. The 'no I inflation' test was conducted on 76 I and 38 E RRUs, of which 29 I RRUs were identified as I alpha and 31 as I beta. Thirteen E RRUs were inhibited and 6 facilitated by preceding lung inflation. Almost all types of respiratory neurons so far reported from different nuclei of cat's brainstem have been located in the NTS region of the rabbit.

Animals↗
PubMed1986

Origin of monoaminergic innervation of the nucleus raphe magnus--a combined monoamine histochemistry and fluorescent retrograde tracing study in the rat.

By the use of the fluorescent retrograde tracer, Fast Blue (FB), in combination with monoamine fluorescence histochemistry, the origin of monoaminergic input to the region of the nucleus raphe magnus (NRM) was investigated in the rat. After microinjection of FB into the NRM, a great number of FB-labeled NA-containing cells were found in the region of the nucleus reticularis lateralis (corresponding to A1 NA areas), the reticular formation just dorsolateral to the nucleus olivaris inferior (corresponding to the A3 NA area), the ventral part of the locus coeruleus (A6 NA area), and the lateral parts of the nucleus raphe dorsalis (B7 area). In the other NA cell groups of the brain stem, FB-labeled cells could not be observed. Serotoninergic input originating from nucleus raphe obscurus (B2), nucleus raphe pallidus (B1) and nucleus raphe pontis (B5-B6) to the NRM was also observed. A large number of cells containing serotonin (5-HT) in the B2 and B6 areas were labeled by FB, while only a few FB-labeled 5-HT cells in B8, B9 were seen. In addition to the FB-labeled monoaminergic (NA and 5-HT) cells, many FB-labeled non-monoamine containing neurons were observed in the nucleus olivaris inferior and various parts of the reticular formation (FR), particularly in the reticular formation of the pons. In conclusion, our study has extended wider the previous HRP finding. It is shown that the NRM receives noradrenergic, serotoninergic and non-monoaminergic innervation from many regions of the brain stem. The afferent projections containing different neurotransmitters provided an important structural basis for studying the function of the NRM.

Amidines↗
PubMed1985

Vagal expiratory afferent discharges during spontaneous breathing.

Expiratory discharges in cervical afferent vagal fibres during spontaneous respiration were observed in anesthetized animals (17 rabbits, 4 cats and 2 monkeys). The percentages of such units among the total observed fibres was 11% in rabbits, 5% in monkeys, 2% in cats. All the experiments were done after section of the recurrent laryngeal nerve and the abdominal branches of the vagus nerve. Changing the intraesophageal pressure from +15 mm Hg to -25 mm Hg by injection or suction of air into or out of the esophagus, of which the abdominal end had been ligated, did not affect the expiratory discharges significantly suggesting that the receptors were not in the esophagus. Injection of air into the lungs to elevate the intratracheal pressure to 5 mm, 10 mm or 15 mm Hg could not excite such receptors. Collapse of the lungs caused by artificial pneumothorax produced continuous discharges in such fibres. Inflation of collapsed lungs by an artificial respiration pump stopped the sustained discharges immediately. The average conduction velocity of the afferent fibres was 25.5 m/s. It seems that this is a type of slowly adapting, low threshold pulmonary receptor with medium sized afferent fibres. The adequate stimulus of such receptors is deflation of the lungs. The possible advantage of participation of such receptors, in addition to the pulmonary stretch (inflation) receptors, in regulation of normal respiration is discussed in the light of the concept of 'paired receptors'.

Animals↗
PubMed1985

Nucleologenesis: composition and fate of prenucleolar bodies.

A time course study was conducted on nucleologenesis after release from a mitotic block in the presence and absence of actinomycin D to determine the composition and fate of prenucleolar bodies (PNBs). Prenucleolar bodies, whether naturally occurring or induced by actinomycin D treatment, stain with silver and contain phosphoproteins B23 and C23, two of the major proteins of the interphase nucleolus as determined by double label immunofluorescence with specific antibodies. The nucleolus is formed by fusion of PNBs, which subsequently "reorganize" and form internal fibrillar and peripheral granular regions. Actinomycin D prevents fusion of PNBs, which are then randomly dispersed throughout the nucleus but they still contain proteins B23 and C23. These results demonstrate that the nucleolus is formed by fusion of prenucleolar structures whose biochemical composition resembles the mature nucleolus, since PNBs contain at least two of the major nucleolar proteins.

Animals↗
PubMed1984

Programmed ventricular stimulation in mitral valve prolapse: analysis of 36 patients.

Programmed ventricular stimulation with 3 extrastimuli was performed in 36 patients with mitral valve prolapse (MVP). Among 11 patients without transient cerebral symptoms, none had inducible ventricular tachycardia (VT) or ventricular fibrillation (VF), whether or not nonsustained VT or ventricular premature complexes (VPC) were present during ambulatory electrocardiographic recordings. These patients remained well without antiarrhythmic drug therapy for 6 to 57 months (mean 23) of follow-up. Two patients with recurrent unexplained syncope and no documented ventricular arrhythmia during electrocardiographic monitoring also had no inducible VT or VF. Among 20 patients with syncope or presyncope and documented nonsustained VT or VPCs during electrocardiographic monitoring, polymorphic nonsustained VT was induced in 8, sustained unimorphic VT in 2, and VF in 3. In 1 patient who had inducible polymorphic nonsustained VT, electrocardiographic monitoring during syncope showed sinus rhythm. Among 3 patients with a history of sustained VT or VF, unimorphic VT was induced in each. Patients with MVP who have asymptomatic ventricular ectopic activity and no inducible VT may have a benign prognosis without treatment. In patients who have transient cerebral symptoms and documented nonsustained VT or VPCs, VT or VF is inducible in 65%, most often polymorphic VT. It is unclear in which patients this finding is clinically significant and in which it is a nonspecific response to programmed stimulation.

Adult↗