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H Aréchiga

Publications and source records attributed to H Aréchiga.

At least 19 recordsLinked to original sources
PubMed1998

Regulation of crustacean neurosecretory cell activity.

1. The X organ-sinus gland system is a conglomerate of 150-200 neurosecretory cells in the eyestalk of crustaceans. It is the source of a host of peptide neurohormones which partake in the control of a wide range of physiological functions. Distinct families of X organ peptides have been chemically characterized: (a) two chromatophorotropic hormones of small sizes, one of 8 residues and the other of 15-20 residues; and (b) three metabotropic hormones of high molecular weight (70-80 residues), related to the control of blood sugar levels, molting, and gonad activity. Some of these hormones have been identified only in crustaceans; others are common to various arthropod groups. A number of peptides orginally described in other zoological groups are also present in the X organ-sinus gland system; such is the case for members of the FMRF-amide family, enkephalins, and other peptides. 2. Cells specifically containing each hormone have been located in the X organ and some information is available on the cellular and molecular substrate of the biosynthesis, transport, storage, and release of various hormones. The electrical activity of X organ neurons has been recorded at the cell soma, arborizations, axons, and neurosecretory terminals. Conspicuous regional differences have been defined for the various patterns of activity, as well as the distribution of their underlying ion currents. 3. The release of hormones and the electrical activity of X organ neurons are regulated by environmental and endogenous influences, such as light and darkness, stress, and circadian rhythms. These influences appear to be mediated by a host of neurotransmitters/modulators, most noticeably, gamma-aminobutyric acid, 5-hydroxytryptamine and other amines, and enkephalins. Each of these mediators acts upon a definite ionic substrate(s) and exerts specific regulatory effects on X organ cell activity. A given neuron may be under the control of more than one neurotransmitter, and a transmitter may mediate different and even opposite influences on different neurons.

Amino Acid Sequence↗
PubMed1997

Seasonal rhythm of red pigment concentrating hormone in the crayfish.

The content of red pigment concentrating hormone (RPCH) in the eye-stalk of the crayfish Procambarus clarkii varies seasonally, with maximum values during the summer months and the lowest values in winter. The responsiveness of tegumentary chromatophores to synthetic RPCH varies concurrently.

Animals↗
PubMed1994

Ultrastructural features of neurosecretory cells in the medulla externa of the crayfish eyestalk.

A conglomerate of 8-12 neurons in the medulla externa of the crayfish eyestalk was explored in their reaction to a polyclonal antibody against the tyrosinated octapeptide Red Pigment Concentrating Hormone (Tyr-RPCH). These are large neurons with diameters within a range of 33-43 microns and they were all positively stained with neutral red. By intracellular staining with lucifer yellow, the neurons were found to branch extensively within the medulla externa and the lamina ganglionaris of the eyestalk. Each neurite bifurcates at about 40 microns from the soma. Both branches run to the medial edge of the eyestalk; one proceeds distally to the lamina ganglionaris, while the other runs proximally to the medulla interna. Both end freely in multiple arborizations, covering from the medial to the lateral edges of the eyestalk. No branches were found to the sinus gland, the main neurohaemal organ of the eyestalk. A group of 4 neurons in the conglomerate consistently rendered positive reaction to the anti-Tyr-RPCH antibody (A-RPCH). They are superficially located in the cluster, and at the electron microscope, they showed the usual features of a secretory cell, i.e., clear and dense granules, an active and well-developed Golgi apparatus, and rough endoplasmic reticulum. The dense granules were larger (mean diameter: 101.5 nm) than the clear granules (mean diameter: 90.3 nm). The immunopositive reaction at the electron microscope was found to be largely confined to the dense-cored granules.

Animals↗
PubMed1994

Regional distribution and immunocytological localization of red pigment concentrating hormone in the crayfish eyestalk.

A polyclonal antibody was raised against synthetic tyrosinated crustacean red pigment concentrating hormone (RPCH-Tyr) with the sequence Tyr-Leu-Asn-Phe-Ser-Pro-Gly-Trp-NH2 with a tryptophan amide at the carboxyl terminal end. Its specificity was tested in comparison with peptides of similar structure. It appears to recognize the three to five residues near the carboxyl terminal. Native RPCH in the crayfish eyestalk was determined by two methods: (a) immunoenzymatic assay (ELISA) using the aforementioned antibody; and (b) bioassay on segments of isolated crayfish tegumentary epithelium. The unitary content in whole eyestalks was 5.5 +/- 1.0 nmol for samples (n = 18) taken at night. The regional distribution of RPCH content in the eyestalk was determined. The greatest proportion (40%) was found in the sinus gland, and the lowest in the retina plus lamina ganglionaris (6%). The medulla interna, medulla externa, and medulla terminalis contained similar proportions (about 16% each). The highest specific content was in the sinus gland (65.0 vs 24.4 pmol/micrograms protein for the whole eyestalk). Immunopositive neurons were identified in the various regions of the eyestalk. In 22 preparations, an average of 7 cells were identified in the ventromedial rim of the medulla terminalis, sending axons to the sinus gland, after branching in the neuropil of the medulla terminalis. Dorsally, 2 cells were identified in the medulla interna and 4 large cells and 11 small cells were located in the medulla externa in close proximity to the lamina ganglionaris: none of these cells appeared to project to the sinus gland. Profuse immunopositive fibers were found in the lamina ganglionaris projecting distally toward the base of the retina. Immunopositive axons were also found in the optic nerve.

Amino Acid Sequence↗
PubMed1994

Excitatory action of gamma-aminobutyric acid (GABA) on crustacean neurosecretory cells.

1. Intracellular and voltage-clamp recordings were obtained from a selected population of neurosecretory (ns) cells in the X organ of the crayfish isolated eyestalk. Pulses of gamma-aminobutyric acid (GABA) elicited depolarizing responses and bursts of action potentials in a dose-dependent manner. These effects were blocked by picrotoxin (50 microM) but not by bicuculline. Picrotoxin also suppressed spontaneous synaptic activity. 2. The responses to GABA were abolished by severing the neurite of X organ cells, at about 150 microns from the cell body. Responses were larger when the application was made at the neuropil level. 3. Topical application of Cd2+ (2 mM), while suppressing synaptic activity, was incapable of affecting the responses to GABA. 4. Under whole-cell voltage-clamp, GABA elicited an inward current with a reversal potential dependent on the chloride equilibrium potential. The GABA effect was accompanied by an input resistance reduction up to 33% at a -50 mV holding potential. No effect of GABA was detected on potassium, calcium, and sodium currents present in X organ cells. 5. The effect of GABA on steady-state currents was dependent on the intracellular calcium concentration. At 10(-6) M [Ca2+]i, GABA (50 microM) increased the membrane conductance more than threefold and shifted the zero-current potential from -25 to -10 mV. At 10(-9) M [Ca2+]i, GABA induced only a 1.3-fold increase in membrane conductance, without shifting the zero-current potential. 6. These results support the notion that in the population of X organ cells sampled in this study, GABA acts as an excitatory neurotransmitter, opening chloride channels.

Action Potentials↗
PubMed1993

Circadian rhythms.

The neurobiological substratum of circadian rhythmicity encompasses three levels of integration: firstly, generation of time signals by circadian pacemakers; secondly, entrainment of pacemakers by environmental influences; thirdly, coupling of circadian pacemakers among themselves and with target systems responsible for the expression of overt rhythms. From recent contributions, the notion that circadian organization results from the interaction of independent oscillators and pathways has been strengthened. In addition, recent evidence supports the existence of circadian rhythmicity in single isolated neurons. New information was produced on the gene control of circadian rhythm generation in Drosophila, as well as interesting advances in the understanding of neuronal mechanisms involved in the generation, entrainment and coupling of circadian rhythms in various species.

Animals↗
PubMed1993

The circadian system of crustaceans.

Crustaceans exhibit a variety of overt circadian rhythms. Observations on intact animals suggest the existence of more than one circadian pacemaker in the nervous system. Ablation experiments so far have been inconclusive in pin-pointing the location of putative pacemakers. However, various structures, most notably the optic peduncle, have been shown to sustain circadian rhythmicity in vitro. Retinal sensitivity and neurosecretory activity display circadian rhythms in the isolated optic peduncle, but they are also responsive to synchronizing influences from other regions of the central nervous system, most notably the supraesophageal ganglion. A model based on a number of circadian pacemakers distributed in the central nervous system best fits the experimental results at present. Coupling of rhythmicity between independent circadian pacemakers is likely to occur, and a neuroendocrine stage of integration has been proposed for several rhythms. Various entraining agents have been identified, and more than one may play a part in the synchronization of a given rhythm.

Animals↗
PubMed1990

Ionic currents in crustacean neurosecretory cells.

1. The patterns of electrical activity and membrane characteristics of a population of neurosecretory-cell somata in the X-organ of the crayfish were investigated with microelectrodes and whole-cell, voltage-clamp techniques. Some neurons (56%) were silent but could be excited by intracellular current injection: other cells showed spontaneous tonic activity (35%), and some had spontaneous bursting activity (9%). The spiking activity was abolished by tetrodotoxin (TTX) exposure and by severing the axon near the cell body. After axotomy, only a small, slow, regenerative depolarization remained that could be blocked by Cd2+. 2. Under voltage clamp the steady-state I-V curve in low [Ca2+]i (9 X 10(-9) M) showed a slope conductance of 16.7 +/- 3.9 (SD) nS (n = 10) at -50 mV and zero current potential of -50.1 +/- 7.7 mV. In current-clamp mode these neurons were either silent or fired tonically. With high [Ca2+]i (1.7 X 10(-6) M) both the slope conductance and inward and outward currents were reduced. In some neurons high [Ca2+]i reveals a negative slope resistance in the range of -46 to -41 mV. It could be supressed by removing [Na+]o, but it was TTX insensitive. These are the neurons that under current clamp showed bursting activity. 3. The main inward current in cell somata was a Ca2+ current of 2 +/- 0.6 nA (n = 18), activated at -40 mV and peaking at 20 mV. It showed relaxation with prolonged pulses. No Na(+)-dependent, TTX-sensitive inward currents were recorded with short (100-ms) pulses in axotomized neurons. 4. Two outward currents could be distinguished.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗
PubMed1990

Modulation of crayfish retinal sensitivity by 5-hydroxytryptamine.

The responsiveness of crayfish retinal photoreceptors to light was enhanced by exposure to 5-hydroxytryptamine (5-HT), either following injection into whole animals or following topical application to isolated eyestalks or retinas. The effect was measured as an increment in the amplitude of the receptor potential, and was dose-dependent in the range 10(-6)-10(-3) mol l-1 (injected as a 0.1 microliter dose in intact animals). It was more pronounced at low levels of illumination and was reversibly blocked by methysergide. The enhancement was a consequence of a dual effect: (a) retraction of the proximal pigment granules within the photoreceptors, with a corresponding increase in the light-admittance function of the retina; and (b) a direct effect, facilitating a membrane conductance increase which mediated the generation of the receptor potential. A set of axons in the lamina ganglionaris with a 5-HT-like immunoreactivity was found in the vicinity of the photoreceptor axons. 5-HT antagonists were capable of blocking the physiological retraction of pigment granules in photoreceptors at night, suggesting that 5-HT acts as a modulator during the nocturnal phase of the circadian cycle in the crayfish retina.

Animals↗
PubMed1989

Behavioral and electrophysiological effects of crustacean neurohormone on freely moving cats.

The behavior of freely moving cats was assessed in an observation chamber during prolonged periods of time. Four patterns of behavior were consistently scored during the mid-day period: a) exploration, b) attention, c) grooming and d) drowsiness. Intracerebroventricular injections of crustacean neurodepressing hormone (NDH) greatly extended the time spent in drowsiness. The threshold dose of NDH for this effect was 300 units. The effect was established a few minutes after the injections and lasted for several hours. During this time the animals sat quietly and showed complete or semicomplete closure of the eyelids. Conspicuous changes in brain electrical activity were also observed under NDH. At low doses, the predominant electrophysiological pattern matches the activity recorded under spontaneous lapses of drowsiness, i.e., spindle bursts in trains of 8-16 Hz in cortical areas and mesencephalic reticular formation. At higher doses, the brain electrical activity changes into a nonconvulsive spiking activity in limbic areas. The time course of the effects differs in the various structures recorded. These results suggest a multiple substrate of NDH activity.

Animals↗
PubMed1988

Influence of substrate on the distribution of calcium channels in identified leech neurons in culture.

The Retzius neuron from the leech, growing in culture on the plant lectin concanavalin A as substrate, produces broad flat growth cones and thick bundles of processes. The same cell extends fine straight processes with numerous branches when grown on a laminin-like substrate extracted from leech central nervous system extracellular matrix, referred to as "leech laminin extract." Cells growing on these two different substrates also show marked differences in the pattern of Ca2+ entry following evoked impulses, as detected optically by local changes in absorbance of the Ca2+-sensitive dye arsenazo III. Ca2+ enters the soma and initial segment of Retzius cells grown on both substrates. However, detectable Ca2+ entry only occurs into the processes of cells growing on leech laminin but not of those growing on concanavalin A. Optical recordings of changes in membrane potential made with the voltage-sensitive dye RH 155 taken from cells growing on either substrate indicate that a depolarization initiated in the soma spreads to the most distant processes with little or no distortion in amplitude or time course. This implies that all voltage-sensitive Ca2+ channels in the cell membrane are equally activated by depolarizing stimuli. Therefore, the fact that impulses evoke Ca2+ entry into processes of Retzius cells grown on leech laminin extract but not of cells grown on concanavalin A shows that the nature of the growth substrate can affect the number and distribution of their functional Ca2+ channels.

Animals↗
PubMed1985

Dye coupling and gap junctions between crustacean neurosecretory cells.

Neurosecretory cells in the X organ-sinus gland system of the crayfish were impaled and Lucifer Yellow was intracellularly iontophoresed. In some neurons the injected dye was transferred to neighboring neurons. The interneuronal dye transfer was between adjacent somata. Coupling was also observed between neurons and smaller cells, possibly glia. Gap junctions were identified by freeze-fracture in neuron somata and glial cells in the X organ and also in neurosecretory axons in the sinus gland.

Astacoidea↗
PubMed1983

Light input to crustacean neurosecretory cells.

Electrical activity was recorded intracellularly from neurosecretory cells in the crayfish eyestalk identified by lucifer yellow injection. The activity is most commonly enhanced by illumination of retinal fields. Increments in spontaneous activity as well as bursts in otherwise silent cells were the most common type of response. Occasionally light-induced inhibitory responses were recorded. At neuropil level, light pulses result in EPSPs with amplitudes dependent on intensity of light and the previous adaptation to darkness.

Animals↗
PubMed1982

Range of modulation of light sensitivity by accessory pigments in the crayfish compound eye.

The compound eye of the crayfish during dark adaptation undergoes an enhancement of light sensitivity within a range of 3 log units. Only 1 log unit can be explained by the increase in responsiveness of the retinula cells. The rest can be accounted for by the migration of the proximal and distal accessory pigments. In isolated retinas, with the distal pigment paralysed in light-adapted position and the proximal pigment only partially responsive, the sensitivity enhancement in darkness is reduced in more than 1 log unit. By hormonally inducing the expansion of the distal pigment while the rest of the system remains dark-adapted, there is a shift of one log unit in the V-log 1 curve. In a crayfish mutant devoid of the two dark accessory pigments, the sensitivity enhancement in dark adaptation only covers one log unit.

Animals↗