scholarly journals The temporal relationship between non-respiratory burst activity of expiratory laryngeal motoneurons and phrenic apnoea during stimulation of the superior laryngeal nerve in rat

2011 ◽  
Vol 589 (7) ◽  
pp. 1819-1830 ◽  
Author(s):  
Qi-Jian Sun ◽  
Tara G. Bautista ◽  
Robert G. Berkowitz ◽  
Wen-Jing Zhao ◽  
Paul M. Pilowsky
Keyword(s):  
Respiratory Burst ◽  
Temporal Relationship ◽  
Superior Laryngeal Nerve ◽  
Laryngeal Nerve ◽  
Burst Activity ◽  
Respiratory Burst Activity ◽  
Laryngeal Motoneurons ◽  
Stimulation Of

Cross-Innervation of the Thyroarytenoid Muscle by a Branch from the External Division of the Superior Laryngeal Nerve

1997 ◽  
Vol 106 (7) ◽  
pp. 594-598 ◽  
Author(s):  
Sina Nasri ◽  
Joel A. Sercarz ◽  
Pouneh Beizai ◽  
Young-Mo Kim ◽  
Ming Ye ◽  
...  
Keyword(s):  
Vocal Fold ◽  
Superior Laryngeal Nerve ◽  
Laryngeal Nerve ◽  
Spasmodic Dysphonia ◽  
Clinical Implications ◽  
Motor Innervation ◽  
Vocal Fold Vibration ◽  
Adductor Spasmodic Dysphonia ◽  
Thyroarytenoid Muscle ◽  
Stimulation Of

The neuroanatomy of the larynx was explored in seven dogs to assess whether there is motor innervation to the thyroarytenoid (TA) muscle from the external division of the superior laryngeal nerve (ExSLN). In 3 animals, such innervation was identified. Electrical stimulation of microelectrodes applied to the ExSLN resulted in contraction of the TA muscle, indicating that this nerve is motor in function. This was confirmed by electromyographic recordings from the TA muscle. Videolaryngostroboscopy revealed improvement in vocal fold vibration following stimulation of the ExSLN compared to without it. Previously, the TA muscle was thought to be innervated solely by the recurrent laryngeal nerve. This additional pathway from the ExSLN to the TA muscle may have important clinical implications in the treatment of neurologic laryngeal disorders such as adductor spasmodic dysphonia.

scholarly journals Neutrophil phagocytosis and respiratory burst activity of dairy cows during the transition period and early lactation

2018 ◽  
Vol 12 (10) ◽  
pp. 894-903
Author(s):  
Marina Žekić-Stošić ◽  
Zdenko Kanački ◽  
Dragica Stojanović ◽  
Dejan Bugarski ◽  
Miodrag Lazarević ◽  
...  
Keyword(s):  
Dairy Cows ◽  
Respiratory Burst ◽  
Transition Period ◽  
Hematological Parameters ◽  
Optimal Level ◽  
Burst Activity ◽  
Early Lactation ◽  
Health Production ◽  
Respiratory Burst Activity ◽  
Entire Study

Introduction: Hormonal and metabolic changes, as well as energy imbalance, can affect health, production and reproductive performance of dairy cows. In the present study, we evaluated phagocytosis and respiratory burst neutrophil activity during the transition period and early lactation and compared it with biochemical and hematological parameters in dairy cows. Methodology: Simmental cows (n = 21) were enrolled in the study. Whole blood samples were collected weekly from 3 weeks pre- calving until 6 weeks post calving. Basic metabolic and blood parameters were assessed by routine laboratory analyses, while neutrophil functions were analyzed by commercial test kits. Results: Optimal neutrophil response was observed pre and post calving. The highest value was recorded in the 6th week after calving (89.54 ± 7.61%) and being significantly higher (p < 0.01) as compared to values recorded at two and one week before and one week after calving. The percentage of activated neutrophils was high during the entire study period: from 70.80 ± 5.22% at the beginning of the study to 89.54 ± 7.61% at the end of the study. During the study period, production of Reactive Oxidative Species by neutrophils was positively correlated with β-hydroxybutyrat and non-esterified fatty acids values (0.454** and 0.423**, respectively) and calcium levels (0.164* and 0.212**, respectively). Conclusions: The most prominent changes in all parameters had no influence on phagocytic and respiratory burst activity of neutrophils. Neutrophil function is preserved at the optimal level during the transition period and early lactation in Simmental cows.

Nucleus tractus solitarius and excitatory amino acids in afferent-evoked inspiratory termination

1994 ◽  
Vol 76 (3) ◽  
pp. 1293-1301 ◽  
Author(s):  
D. R. Karius ◽  
L. Ling ◽  
D. F. Speck
Keyword(s):  
Nmda Receptors ◽  
Nucleus Tractus Solitarius ◽  
Excitatory Amino Acid ◽  
Superior Laryngeal Nerve ◽  
Nmda Antagonist ◽  
Intercostal Nerve ◽  
Laryngeal Nerve ◽  
Receptor Antagonists ◽  
Adult Cats ◽  
Stimulation Of

This study tested the hypothesis that excitatory amino acid (EAA) neurotransmission at non-N-methyl-D-aspartate (non-NMDA), but not NMDA, receptors within medial regions of the nucleus tractus solitarius (NTS) is required in the inspiratory termination elicited by vagal or intercostal nerve (ICN) stimulation. Adult cats were anesthetized, decerebrated, vagotomized, and ventilated. After control responses to stimulation of the superior laryngeal nerve (SLN), vagus, and ICN were obtained, EAA receptor antagonists were injected into the medial aspects of the NTS. Injections of 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) or 6,7-dinitro-quinoxaline-2,3-dione (DNQX), EAA receptor antagonists; (+/-)-2-amino-5-phosphonopentanoic acid (AP5), an NMDA antagonist; or 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(F)quinoxaline (NBQX), a non-NMDA antagonist, ipsilateral to the vagus abolished the termination response. The SLN-elicited response persisted after AP5 injection but was abolished by NBQX injections. The ICN-elicited response persisted after bilateral injections of CNQX/DNQX or procaine. We conclude that the inspiratory termination elicited by ICN stimulation is independent of the regions medial to the NTS. Inspiratory termination elicited by vagal or SLN stimulation requires non-NMDA-mediated EAA neurotransmission within medial aspects of the NTS, but the vagally elicited response also requires NMDA receptors.

Ketamine inhibits polymorphonuclear leucocyte CD11b expression and respiratory burst activity in endotoxemic rats

2007 ◽  
Vol 56 (4) ◽  
pp. 149-153 ◽  
Author(s):  
Z. Q. Zhou ◽  
Y. Q. Yu ◽  
S. W. Feng ◽  
M. Yu ◽  
H. J. Liu ◽  
...  
Keyword(s):  
Respiratory Burst ◽  
Polymorphonuclear Leucocyte ◽  
Burst Activity ◽  
Respiratory Burst Activity ◽  
Cd11b Expression

Influences of superior laryngeal afferent stimulation on expiratory activity in cats

1988 ◽  
Vol 65 (1) ◽  
pp. 385-392 ◽  
Author(s):  
F. Bongianni ◽  
M. Corda ◽  
G. Fontana ◽  
T. Pantaleo
Keyword(s):  
Superior Laryngeal Nerve ◽  
Laryngeal Nerve ◽  
Tetanic Stimulation ◽  
Bötzinger Complex ◽  
Dependent Activity ◽  
Inspiratory Activity ◽  
Polysynaptic Reflex ◽  
Expiratory Muscles ◽  
Excitatory Responses ◽  
Stimulation Of

The effects of superior laryngeal nerve (SLN) stimulation on the activity of the expiratory muscles and medullary expiration-related (ER) neurons were investigated in 24 pentobarbital-anesthetized cats. In some experiments the animals were also paralyzed and artificially ventilated. Sustained tetanic stimulation of SLN consistently caused an apneic response associated with the appearance of tonic CO2-dependent activity in the expiratory muscles and in ER neurons located in the caudal ventral respiratory group (VRG) and the Botzinger complex. Single shocks or brief tetani at the same stimulation intensities failed to evoke excitatory responses in the expiratory muscles and in the vast majority of ER neurons tested. At higher stimulation strengths, single shocks or short tetani elicited excitatory responses in the expiratory muscles (20- to 35-ms latency) and in the majority of ER neurons of the caudal VRG (7.5- to 15.5-ms latency). These responses were obtained only during the expiratory phase and proved to be CO2 independent. On the contrary, only inhibitory responses were evoked in the activity of Botzinger complex neurons. The observed tonic expiratory activity most likely represents a disinhibition phenomenon due to the suppression of inspiratory activity; activation of expiratory muscles at higher stimulation intensities appears to be a polysynaptic reflex mediated by ER neurons of the caudal VRG but not by Botzinger complex neurons.

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