scholarly journals Stress related network activity in the intact adrenal medulla

2021 ◽  
Author(s):  
Jose R. Lopez Ruiz ◽  
Stephen A. Ernst ◽  
Ronald W. Holz ◽  
Edward L. Stuenkel

AbstractThe adrenal medulla has long been recognized as playing a critical role in mammalian homeostasis and the stress response. The adrenal medulla is populated by clustered chromaffin cells that secrete epinephrine or norepinephrine along with other peptides into the general bloodstream affecting multiple distant target organs. Although the sympatho-adrenal pathway has been heavily studied, detailed knowledge on the central control and in-situ spatiotemporal responsiveness remains poorly understood. For this work we implemented electrophysiological techniques originally developed to elucidate CNS circuitry to characterize the functional micro-architecture of the adrenal medulla. To achieve this, we continuously monitored the electrical activity inside the adrenal medulla in the living anesthetized rat under basal conditions and under physiological stress. Under basal conditions, chromaffin cells fired action potentials with frequencies between ∼0.2 and 4 Hz. Activity was exclusively driven by sympathetic inputs coming through the splanchnic nerve. Furthermore, chromaffin cells were organized into arrays of independent local networks in which cells fire in a specific order, with latencies from hundreds of microseconds to few milliseconds. Electrical stimulation of the splanchnic nerve evoked the exact same spatiotemporal firing patterns that occurred spontaneously. Induction of hypoglycemic stress by administration of insulin resulted in an increase in the activity of a subset of the chromaffin cell networks. In contrast, respiratory arrest induced by anesthesia overdose resulted in an increase in the activity of the entire adrenal medulla before cessation of all activity when the animal died. The results suggest the differential activation of specific networks inside the adrenal gland depending on the stressor. These results revealed a surprisingly complex electrical organization and circuitry of the adrenal medulla that likely reflects the dynamic nature of its neuroendocrine output during basal conditions and during different types of physiological stress. To our knowledge, these experiments are the first to use multi-electrode arrays in vivo to examine the electrical and functional architecture of any endocrine gland.Significance StatementStress from extrinsic (environmental, psychological) and intrinsic (biological) challenges plays a critical role in disturbing the homeostatic balance. While the body’s responses to stress are designed to ameliorate these imbalances, prolonged and dysregulated stress often drives adverse health consequences in many chronic illnesses. The better understanding of the sympatho-adrenal stress response, will potentially impact and improve the treatment of several stress related illnesses. This work focusses on the study of the functional architecture of the adrenal medulla, a key component in neuronal stress response.

Stroke ◽  
2017 ◽  
Vol 48 (suppl_1) ◽  
Author(s):  
Azadeh Yazdan-Shahmorad ◽  
Jiwei He ◽  
Kenny Kay ◽  
Gratianne Rabiller ◽  
Yasuo Nishijima ◽  
...  

Introduction: The mechanism underlying post-stroke cognitive impairment is not well understood. The hippocampus is involved in memory function yet remains structurally intact after cortical stroke. During the slow-wave state, the hippocampus exhibits Sharp-wave associated ripples (SPW-Rs), a high-frequency activity in the pyramidal layer of the hippocampal CA1 that plays a critical role in memory consolidation. However, it is unclear whether cortical stroke chronically affects SPW-Rs or any other hippocampal oscillations. Hypothesis: Stroke affects network oscillations that bind neurons into transient assemblies with coherent activity. Methods: Adult male rats (n=28) were subjected to distal middle cerebral artery occlusion (dMCAO), compared to controls (n=19) by sham-operation. After time periods of either two weeks or one month, we recorded the neural activity from different depths starting at deep cortical layers down to hippocampus using 16-site linear electrode arrays under urethane anesthesia. We defined two states of high theta (HT) and low theta (LT) by calculating the ratio of Hilbert amplitudes of theta (4-7 Hz) to delta (0.1-3 Hz) filtered local field potential (LFP) recorded from the CA1 stratum lacunosum moleculare. A threshold was manually set to capture sustained periods in which the theta:delta ratio was elevated. Periods of SWRs were also detected from the filtered LFP (150-250Hz) recordings of CA1 pyramidal layer. Results: Chronic stroke increased the frequency of alternation between HT and LT states by shortening the duration of HT states. Stroke also increased the rate of occurrence of SWRs during LT state. Furthermore, chronic stroke at one month reduced theta and delta power at the hippocampal pyramidal layer and the cortex ipsilaterally, while it reduced gamma power bilaterally in the pyramidal layer during the HT states. Conclusions: Ischemic stroke affects brain states and several major oscillations not only in the cortex but also in the hippocampus. The aberrant brain oscillation may disrupt neural network activity that gives rise to complex cognitive behaviors, underlying post stroke cognitive impairment.


2010 ◽  
Vol 298 (2) ◽  
pp. C397-C405 ◽  
Author(s):  
Antonio M. G. de Diego

The ability of adrenal chromaffin cells to fast-release catecholamines relies on their capacity to fire action potentials (APs). However, little attention has been paid to the requirements needed to evoke the controlled firing of APs. Few data are available in rodents and none on the bovine chromaffin cell, a model extensively used by researchers. The aim of this work was to clarify this issue. Short puffs of acetylcholine (ACh) were fast perifused to current-clamped chromaffin cells and produced the firing of single APs. Based on the currents generated by such ACh applications and previous literature, current waveforms that efficiently elicited APs at frequencies up to 20 Hz were generated. Complex waveforms were also generated by adding simple waveforms with different delays; these waveforms aimed at modeling the stimulation patterns that a chromaffin cell would conceivably undergo upon strong synaptic stimulation. Cholinergic innervation was assessed using the acetylcholinesterase staining technique on the supposition that the innervation pattern is a determinant of the kind of stimuli chromaffin cells can receive. It is concluded that 1) a reliable method to produce frequency-controlled APs by applying defined current injection waveforms is achieved; 2) the APs thus generated have essentially the same features as those spontaneously emitted by the cell and those elicited by fast-ACh perifusion; 3) the higher frequencies attainable peak at around 30 Hz; and 4) the bovine adrenal medulla shows abundant cholinergic innervation, and chromaffin cells show strong acetylcholinesterase staining, consistent with a tight cholinergic presynaptic control of firing frequency.


2004 ◽  
Vol 287 (1) ◽  
pp. R161-R166 ◽  
Author(s):  
Tsuyoshi Akiyama ◽  
Toji Yamazaki ◽  
Hidezo Mori ◽  
Kenji Sunagawa

To elucidate the types of voltage-dependent Ca2+ channels controlling ACh and catecholamine releases in the in vivo adrenal medulla, we implanted microdialysis probes in the left adrenal medulla of anesthetized rats and investigated the effects of Ca2+ channel antagonists on ACh, norepinephrine, and epinephrine releases induced by nerve stimulation. The dialysis probes were perfused with Ringer solution containing a cholinesterase inhibitor, neostigmine. The left splanchnic nerves were electrically stimulated at 2 and 4 Hz before and after intravenous administration of Ca2+ channel antagonists. ω-Conotoxin GVIA (an N-type Ca2+ channel antagonist, 10 μg/kg) inhibited ACh release at 2 and 4 Hz by ∼40%, norepinephrine release at 4 Hz by ∼50%, and epinephrine release at 2 and 4 Hz by ∼45%. A fivefold higher dose of ω-conotoxin GVIA (50 μg/kg) did not further inhibit these releases. ω-Conotoxin MVIIC (a P/Q-type Ca2+ channel antagonist, 50 μg/kg) inhibited ACh and epinephrine releases at 4 Hz by ∼30%. Combined ω-conotoxin GVIA (50 μg/kg) and MVIIC (250 μg/kg) inhibited ACh release at 2 and 4 Hz by ∼70% and norepinephrine and epinephrine releases at 2 and 4 Hz by ∼80%. Nifedipine (an L-type Ca2+ channel antagonist, 300 and 900 μg/kg) did not change ACh release at 2 and 4 Hz; however, nifedipine (300 μg/kg) inhibited epinephrine release at 4 Hz by 20%, and nifedipine (900 μg/kg) inhibited norepinephrine and epinephrine releases at 4 Hz by 30%. In conclusion, both N- and P/Q-type Ca2+ channels control ACh release on preganglionic splanchnic nerve endings while L-type Ca2+ channels do not. L-type Ca2+ channels are involved in norepinephrine and epinephrine releases on chromaffin cells.


Author(s):  
Gemma A.J. Kuijpers ◽  
Harvey B. Pollard

Exocytotic fusion of granules in the adrenal medulla chromaffin cell is triggered by a rise in the concentration of cytosolic Ca2+ upon cell activation. The protein synexin, annexin VII, was originally found in the adrenal medulla and has been shown to cause aggregation and to support fusion of chromaffin granules in a Ca2+-dependent manner. We have previously suggested that synexin may there fore play a role in the exocytotic fusion process. In order to obtain more structural information on synexin, we performed immuno-electron microscopy on frozen ultrathin sections of both isolated chromaffin granules and chromaffin cells.Chromaffin granules were isolated from bovine adrenal medulla, and synexin was isolated from bovine lung. Granules were incubated in the presence or absence of synexin (24 μg per mg granule protein) and Ca2+ (1 mM), which induces maximal granule aggregation, in 0.3M sucrose-40m MMES buffer(pH 6.0). Granules were pelleted, washed twice in buffer without synexin and fixed with 2% glutaraldehyde- 2% para formaldehyde in 0.1 M phosphate buffer (GA/PFA) for 30 min. Chromaffin cells were isolated and cultured for 3-5 days, and washed and incubated in Krebs solution with or without 20 uM nicotine. Cells were fixed 90 sec after on set of stimulation with GA/PFA for 30 min. Fixed granule or cell pellets were washed, infiltrated with 2.3 M sucrose in PBS, mounted and frozen in liquid N2.


BIOspektrum ◽  
2021 ◽  
Vol 27 (4) ◽  
pp. 390-393
Author(s):  
F.-Nora Vögtle

AbstractThe majority of mitochondrial proteins are encoded in the nuclear genome, so that the nearly entire proteome is assembled by post-translational preprotein import from the cytosol. Proteomic imbalances are sensed and induce cellular stress response pathways to restore proteostasis. Here, the mitochondrial presequence protease MPP serves as example to illustrate the critical role of mitochondrial protein biogenesis and proteostasis on cellular integrity.


2021 ◽  
Vol 239 ◽  
pp. 105940
Author(s):  
Laura Simões Andrade ◽  
Domingos Garrone-Neto ◽  
Manuela Alves Nobre Sales ◽  
Luciana Rodrigues de Souza-Bastos ◽  
Ursulla Pereira Souza ◽  
...  

2019 ◽  
Vol 20 (19) ◽  
pp. 4901 ◽  
Author(s):  
Leonardo M. R. Ferreira ◽  
Teresa Cunha-Oliveira ◽  
Margarida C. Sobral ◽  
Patrícia L. Abreu ◽  
Maria Carmen Alpoim ◽  
...  

Worldwide, several million workers are employed in the various chromium (Cr) industries. These workers may suffer from a variety of adverse health effects produced by dusts, mists and fumes containing Cr in the hexavalent oxidation state, Cr(VI). Of major importance, occupational exposure to Cr(VI) compounds has been firmly associated with the development of lung cancer. Counterintuitively, Cr(VI) is mostly unreactive towards most biomolecules, including nucleic acids. However, its intracellular reduction produces several species that react extensively with biomolecules. The diversity and chemical versatility of these species add great complexity to the study of the molecular mechanisms underlying Cr(VI) toxicity and carcinogenicity. As a consequence, these mechanisms are still poorly understood, in spite of intensive research efforts. Here, we discuss the impact of Cr(VI) on the stress response—an intricate cellular system against proteotoxic stress which is increasingly viewed as playing a critical role in carcinogenesis. This discussion is preceded by information regarding applications, chemical properties and adverse health effects of Cr(VI). A summary of our current understanding of cancer initiation, promotion and progression is also provided, followed by a brief description of the stress response and its links to cancer and by an overview of potential molecular mechanisms of Cr(VI) carcinogenicity.


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