Functional significance and neural basis of larval lamprey startle behaviour

1987 ◽  
Vol 133 (1) ◽  
pp. 121-135 ◽  
Author(s):  
S. N. Currie ◽  
R. C. Carlsen

1. The vibration-evoked startle response mediates rapid withdrawal in burrowed larval lampreys (ammocoetes). Ammocoetes withdraw in response to vibration by contracting pre-existing lateral bends in the trunk and tail, thus pulling their heads deeper into the burrow. 2. The motor effects of an ammocoete startle response are dependent on pre-existing posture. Areas of lateral body curvature contract more and exhibit larger electromyogram (EMG) amplitudes on their inner sides than on their outer sides. 3. Both of the anterior Mth and posterior Mth' (Mauthner) cells and both of the B1 and B2 (bulbar) Muller cells fired action potentials in response to vibration of the otic capsules. Both B3 and B4 Muller cells were inhibited by vibration, while M (mesencephalic) and I1 (isthmic) Muller cells were inhibited by ipsilateral vibration and excited by contralateral vibration. 4. Simultaneous action potentials in both of the anterior Mth cells were appropriate and sufficient for initiating the startle response EMG in a semi-intact preparation. 5. This study demonstrates a Mauthner-initiated startle response which activates musculature on both sides of the body to produce a rapid withdrawal movement and is thus adapted to the eel-like form and burrowed lifestyle of larval lampreys.

2008 ◽  
Vol 411 (1) ◽  
pp. 79-88 ◽  
Author(s):  
Jaya P. Gnana-Prakasam ◽  
Pamela M. Martin ◽  
Barbara A. Mysona ◽  
Penny Roon ◽  
Sylvia B. Smith ◽  
...  

Hepcidin is a hormone central to the regulation of iron homeostasis in the body. It is believed to be produced exclusively by the liver. Ferroportin, an iron exporter, is the receptor for hepcidin. This transporter/receptor is expressed in Müller cells, photoreceptor cells and the RPE (retinal pigment epithelium) within the retina. Since the retina is protected by the retinal–blood barriers, we asked whether ferroportin in the retina is regulated by hepcidin in the circulation or whether the retina produces hepcidin for regulation of its own iron homeostasis. Here we show that hepcidin is expressed robustly in Müller cells, photoreceptor cells and RPE cells, closely resembling the expression pattern of ferroportin. We also show that bacterial LPS (lipopolysaccharide) is a regulator of hepcidin expression in Müller cells and the RPE, both in vitro and in vivo, and that the regulation occurs at the transcriptional level. The action of LPS on hepcidin expression is mediated by the TLR4 (Toll-like receptor-4). The upregulation of hepcidin by LPS occurs independent of Hfe (human leukocyte antigen-like protein involved in Fe homeostasis). The increase in hepcidin levels in retinal cells in response to LPS treatment is associated with a decrease in ferroportin levels. The LPS-induced upregulation of hepcidin and consequent down-regulation of ferroportin is associated with increased oxidative stress and apoptosis within the retina in vivo. We conclude that retinal iron homeostasis may be regulated in an autonomous manner by hepcidin generated within the retina and that chronic bacterial infection/inflammation of the retina may disrupt iron homeostasis and retinal function.


2018 ◽  
Vol 17 (4) ◽  
pp. 255-260 ◽  
Author(s):  
Feng Gao ◽  
Lin-Jie Xu ◽  
Yuan Zhao ◽  
Xing-Huai Sun ◽  
Zhongfeng Wang

Background & Objective: Müller cell is the major type of glial cell in the vertebrate retina. Müller cells express various types of K+ channels, such as inwardly rectifying K+ (Kir) channels, big conductance Ca2+-activated K+ (BKCa) channels, delayed rectifier K+ channels (KDR), and transient A-type K+ channels. These K+ channels play important roles in maintaining physiological functions of Müller cells. Under some retinal pathological conditions, the changed expression and functions of K+ channels may contribute to retinal pathogenesis. Conclusion: In this article, we reviewed the physiological properties of K+ channels in retinal Müller cells and the functional changes of these channels in retinal disorders.


2021 ◽  
Vol 137 ◽  
pp. 111274
Author(s):  
Yuanyuan Tu ◽  
E Song ◽  
Zhenzhen Wang ◽  
Na Ji ◽  
Linling Zhu ◽  
...  

Author(s):  
Adwaid Manu Krishna Chandran ◽  
Daniela Coltrini ◽  
Mirella Belleri ◽  
Sara Rezzola ◽  
Elena Gambicorti ◽  
...  

2007 ◽  
Vol 104 (20) ◽  
pp. 8287-8292 ◽  
Author(s):  
K. Franze ◽  
J. Grosche ◽  
S. N. Skatchkov ◽  
S. Schinkinger ◽  
C. Foja ◽  
...  

Glia ◽  
2010 ◽  
Vol 59 (2) ◽  
pp. 256-266 ◽  
Author(s):  
Anett Karl ◽  
Antje Wurm ◽  
Thomas Pannicke ◽  
Katja Krügel ◽  
Marta Obara-Michlewska ◽  
...  

2010 ◽  
Vol 91 (1) ◽  
pp. 34-41 ◽  
Author(s):  
Susan E. Yanni ◽  
Gary W. McCollum ◽  
John S. Penn

1997 ◽  
Vol 25 (2) ◽  
pp. 251S-251S ◽  
Author(s):  
William Russell ◽  
Robert D. Hollifield ◽  
Adam J. West ◽  
Miles R. Stanford ◽  
G. Astrid Limb

2002 ◽  
Vol 70 (2) ◽  
pp. 209-218 ◽  
Author(s):  
Ortrud Uckermann ◽  
Jens Grosche ◽  
Andreas Reichenbach ◽  
Andreas Bringmann

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