Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.

The sympathetic nervous system is critical in maintaining the normal physiological function of the heart. Its dysfunction in pathological states may exacerbate the substrate for arrhythmias. Obviously, knowledge of its three-dimensional (3D) structure is important, however, it has been revealed by c...

Full description

Bibliographic Details
Main Authors: Teruki Yokoyama, Jong-Kook Lee, Keiko Miwa, Tobias Opthof, Satoki Tomoyama, Hiroyuki Nakanishi, Akira Yoshida, Haruyo Yasui, Tadatsune Iida, Shigeru Miyagawa, Shigeo Okabe, Yoshiki Sawa, Yasushi Sakata, Issei Komuro
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5533449?pdf=render
id doaj-3017984c8c494c0284f57a28fa1a266e
record_format Article
spelling doaj-3017984c8c494c0284f57a28fa1a266e2020-11-24T20:40:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01127e018207210.1371/journal.pone.0182072Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.Teruki YokoyamaJong-Kook LeeKeiko MiwaTobias OpthofSatoki TomoyamaHiroyuki NakanishiAkira YoshidaHaruyo YasuiTadatsune IidaShigeru MiyagawaShigeo OkabeYoshiki SawaYasushi SakataIssei KomuroThe sympathetic nervous system is critical in maintaining the normal physiological function of the heart. Its dysfunction in pathological states may exacerbate the substrate for arrhythmias. Obviously, knowledge of its three-dimensional (3D) structure is important, however, it has been revealed by conventional methods only to a limited extent. In this study, a new method of tissue clearance in combination with immunostaining unravels the 3D structure of the sympathetic cardiac network as well as its changes after myocardial infarction.Hearts isolated from adult male mice were optically cleared using the CUBIC-perfusion protocol. After making the hearts transparent, sympathetic nerves and coronary vessels were immunofluorescently labeled, and then images were acquired. The spatial distribution of sympathetic nerves was visualized not only along the epicardial surface, but also transmurally. They were distributed over the epicardial surface and penetrated into the myocardium to twist around coronary vessels, but also independent from the coronary vasculature. At 2 weeks after myocardial infarction, we were able to quantify both denervation distal from the site of infarction and nerve sprouting (hyperinnervation) at the ischemic border zone of the hearts in a 3D manner. The nerve density at the ischemic border zone was more than doubled in hearts with myocardial infarction compared to intact mice hearts (3D analyses; n = 5, p<0.05).There is both sympathetic hyperinnervation and denervation after myocardial infarction. Both can be visualized and quantified by a new imaging technique in transparent hearts and thereby become a useful tool in elucidating the role of the sympathetic nervous system in arrhythmias associated with myocardial infarction.http://europepmc.org/articles/PMC5533449?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Teruki Yokoyama
Jong-Kook Lee
Keiko Miwa
Tobias Opthof
Satoki Tomoyama
Hiroyuki Nakanishi
Akira Yoshida
Haruyo Yasui
Tadatsune Iida
Shigeru Miyagawa
Shigeo Okabe
Yoshiki Sawa
Yasushi Sakata
Issei Komuro
spellingShingle Teruki Yokoyama
Jong-Kook Lee
Keiko Miwa
Tobias Opthof
Satoki Tomoyama
Hiroyuki Nakanishi
Akira Yoshida
Haruyo Yasui
Tadatsune Iida
Shigeru Miyagawa
Shigeo Okabe
Yoshiki Sawa
Yasushi Sakata
Issei Komuro
Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
PLoS ONE
author_facet Teruki Yokoyama
Jong-Kook Lee
Keiko Miwa
Tobias Opthof
Satoki Tomoyama
Hiroyuki Nakanishi
Akira Yoshida
Haruyo Yasui
Tadatsune Iida
Shigeru Miyagawa
Shigeo Okabe
Yoshiki Sawa
Yasushi Sakata
Issei Komuro
author_sort Teruki Yokoyama
title Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
title_short Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
title_full Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
title_fullStr Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
title_full_unstemmed Quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
title_sort quantification of sympathetic hyperinnervation and denervation after myocardial infarction by three-dimensional assessment of the cardiac sympathetic network in cleared transparent murine hearts.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description The sympathetic nervous system is critical in maintaining the normal physiological function of the heart. Its dysfunction in pathological states may exacerbate the substrate for arrhythmias. Obviously, knowledge of its three-dimensional (3D) structure is important, however, it has been revealed by conventional methods only to a limited extent. In this study, a new method of tissue clearance in combination with immunostaining unravels the 3D structure of the sympathetic cardiac network as well as its changes after myocardial infarction.Hearts isolated from adult male mice were optically cleared using the CUBIC-perfusion protocol. After making the hearts transparent, sympathetic nerves and coronary vessels were immunofluorescently labeled, and then images were acquired. The spatial distribution of sympathetic nerves was visualized not only along the epicardial surface, but also transmurally. They were distributed over the epicardial surface and penetrated into the myocardium to twist around coronary vessels, but also independent from the coronary vasculature. At 2 weeks after myocardial infarction, we were able to quantify both denervation distal from the site of infarction and nerve sprouting (hyperinnervation) at the ischemic border zone of the hearts in a 3D manner. The nerve density at the ischemic border zone was more than doubled in hearts with myocardial infarction compared to intact mice hearts (3D analyses; n = 5, p<0.05).There is both sympathetic hyperinnervation and denervation after myocardial infarction. Both can be visualized and quantified by a new imaging technique in transparent hearts and thereby become a useful tool in elucidating the role of the sympathetic nervous system in arrhythmias associated with myocardial infarction.
url http://europepmc.org/articles/PMC5533449?pdf=render
work_keys_str_mv AT terukiyokoyama quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT jongkooklee quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT keikomiwa quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT tobiasopthof quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT satokitomoyama quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT hiroyukinakanishi quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT akirayoshida quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT haruyoyasui quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT tadatsuneiida quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT shigerumiyagawa quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT shigeookabe quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT yoshikisawa quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT yasushisakata quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
AT isseikomuro quantificationofsympathetichyperinnervationanddenervationaftermyocardialinfarctionbythreedimensionalassessmentofthecardiacsympatheticnetworkinclearedtransparentmurinehearts
_version_ 1716827342553219072