Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
by
Mitchell, Gordon S.
, Roberts, Brandon M.
, Judge, Andrew R.
, Fields, Daryl P.
, Fuller, David D.
, Simon, Alec K.
in
Animals
/ Body temperature
/ Breathing
/ Cachexia - physiopathology
/ Cancer
/ Cancer therapies
/ Carbon dioxide
/ Cell Line, Tumor
/ Chemoreflex and hypoxia
/ Hypercapnia
/ Hypoxia
/ Hypoxia - physiopathology
/ Laboratories
/ Male
/ Mice
/ Mortality
/ Neoplasms - physiopathology
/ Neuropathology
/ Original
/ Phrenic Nerve - physiology
/ Plethysmography
/ Respiration
/ Software
/ Variance analysis
/ Ventilation
2019
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
by
Mitchell, Gordon S.
, Roberts, Brandon M.
, Judge, Andrew R.
, Fields, Daryl P.
, Fuller, David D.
, Simon, Alec K.
in
Animals
/ Body temperature
/ Breathing
/ Cachexia - physiopathology
/ Cancer
/ Cancer therapies
/ Carbon dioxide
/ Cell Line, Tumor
/ Chemoreflex and hypoxia
/ Hypercapnia
/ Hypoxia
/ Hypoxia - physiopathology
/ Laboratories
/ Male
/ Mice
/ Mortality
/ Neoplasms - physiopathology
/ Neuropathology
/ Original
/ Phrenic Nerve - physiology
/ Plethysmography
/ Respiration
/ Software
/ Variance analysis
/ Ventilation
2019
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
by
Mitchell, Gordon S.
, Roberts, Brandon M.
, Judge, Andrew R.
, Fields, Daryl P.
, Fuller, David D.
, Simon, Alec K.
in
Animals
/ Body temperature
/ Breathing
/ Cachexia - physiopathology
/ Cancer
/ Cancer therapies
/ Carbon dioxide
/ Cell Line, Tumor
/ Chemoreflex and hypoxia
/ Hypercapnia
/ Hypoxia
/ Hypoxia - physiopathology
/ Laboratories
/ Male
/ Mice
/ Mortality
/ Neoplasms - physiopathology
/ Neuropathology
/ Original
/ Phrenic Nerve - physiology
/ Plethysmography
/ Respiration
/ Software
/ Variance analysis
/ Ventilation
2019
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
Journal Article
Cancer cachexia impairs neural respiratory drive in hypoxia but not hypercapnia
2019
Request Book From Autostore
and Choose the Collection Method
Overview
Background Cancer cachexia is an insidious process characterized by muscle atrophy with associated motor deficits, including diaphragm weakness and respiratory insufficiency. Although neuropathology contributes to muscle wasting and motor deficits in many clinical disorders, neural involvement in cachexia‐linked respiratory insufficiency has not been explored. Methods We first used whole‐body plethysmography to assess ventilatory responses to hypoxic and hypercapnic chemoreflex activation in mice inoculated with the C26 colon adenocarcinoma cell line. Mice were exposed to a sequence of inspired gas mixtures consisting of (i) air, (ii) hypoxia (11% O2) with normocapnia, (iii) hypercapnia (7% CO2) with normoxia, and (iv) combined hypercapnia with hypoxia (i.e. maximal chemoreflex response). We also tested the respiratory neural network directly by recording inspiratory burst output from ligated phrenic nerves, thereby bypassing influences from changes in diaphragm muscle strength, respiratory mechanics, or compensation through recruitment of accessory motor pools. Results Cachectic mice demonstrated a significant attenuation of the hypoxic tidal volume (0.26mL±0.01mL vs 0.30mL±0.01mL; p<0.05), breathing frequency (317±10bpm vs 344±6bpm; p<0.05) and phrenic nerve (29.5±2.6% vs 78.8±11.8%; p<0.05) responses. On the other hand, the much larger hypercapnic tidal volume (0.46±0.01mL vs 0.46±0.01mL; p>0.05), breathing frequency (392±5bpm vs 408±5bpm; p>0.05) and phrenic nerve (93.1±8.8% vs 111.1±13.2%; p>0.05) responses were not affected. Further, the concurrent hypercapnia/hypoxia tidal volume (0.45±0.01mL vs 0.45±0.01mL; p>0.05), breathing frequency (395±7bpm vs 400±3bpm; p>0.05), and phrenic nerve (106.8±7.1% vs 147.5±38.8%; p>0.05) responses were not different between C26 cachectic and control mice. Conclusions Breathing deficits associated with cancer cachexia are specific to the hypoxic ventilatory response and, thus, reflect disruptions in the hypoxic chemoafferent neural network. Diagnostic techniques that detect decompensation and therapeutic approaches that support the failing hypoxic respiratory response may benefit patients at risk for cancer cachectic‐associated respiratory failure.
This website uses cookies to ensure you get the best experience on our website.