{"title":"Accelerating effects of blebbistatin on relaxation process of cell membrane permeabilized trachea and taenia cecum from guinea pig.","authors":"Satoko Mihashi, Yukisato Ishida, Masaru Watanabe","doi":"10.1540/jsmr.56.19","DOIUrl":"https://doi.org/10.1540/jsmr.56.19","url":null,"abstract":"<p><p>Blebbistatin, a potent inhibitor of myosin II, is known to suppress smooth muscle contraction without affecting myosin light chain phosphorylation level. In order to clarify the regulatory mechanisms of blebbistatin on phasic and tonic smooth muscles in detail, we examined the effects of blebbistatin on relaxation process by Ca<sup>2+</sup> removal after Ca<sup>2+</sup>-induced contraction of β-escin skinned (cell membrane permeabilized) trachea and taenia cecum preparations from guinea pigs. Blebbistatin significantly suppressed the force during relaxation both in skinned trachea and taenia cecum. The data fitting analysis of the relaxation processes indicates that blebbistatin accelerates slow (latch-like) bridge dissociation.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"56 0","pages":"19-28"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/72/b1/jsmr-56-019.PMC7184228.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37885871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sang Eok Lee, Dae Hoon Kim, Seung Myeung Son, Song-Yi Choi, Ra Young You, Chan Hyung Kim, Woong Choi, Hun Sik Kim, Yung Ji Lim, Ji Young Han, Hyun Woo Kim, In Jun Yang, Wen-Xie Xu, Sang Jin Lee, Young Chul Kim, Hyo-Yung Yun
{"title":"Physiological function and molecular composition of ATP-sensitive K<sup>+</sup> channels in human gastric smooth muscle.","authors":"Sang Eok Lee, Dae Hoon Kim, Seung Myeung Son, Song-Yi Choi, Ra Young You, Chan Hyung Kim, Woong Choi, Hun Sik Kim, Yung Ji Lim, Ji Young Han, Hyun Woo Kim, In Jun Yang, Wen-Xie Xu, Sang Jin Lee, Young Chul Kim, Hyo-Yung Yun","doi":"10.1540/jsmr.56.29","DOIUrl":"https://doi.org/10.1540/jsmr.56.29","url":null,"abstract":"<p><p>Gastric motility is controlled by slow waves. In general, the activation of the ATP-sensitive K<sup>+</sup> (K<sub>ATP</sub>) channels in the smooth muscle opposes the membrane excitability and produces relaxation. Since metabolic inhibition and/or diabetes mellitus are accompanied by dysfunctions of gastric smooth muscle, we examined the possible roles of K<sub>ATP</sub> channels in human gastric motility. We used human gastric corpus and antrum smooth muscle preparations and recorded the mechanical activities with a conventional contractile measuring system. We also identified the subunits of the K<sub>ATP</sub> channels using Western blot. Pinacidil (10 μM), a K<sub>ATP</sub> channel opener, suppressed contractions to 30% (basal tone to -0.2 g) of the control. The inhibitory effect of pinacidil on contraction was reversed to 59% of the control by glibenclamide (20 μM), a K<sub>ATP</sub> channel blocker. The relaxation by pinacidil was not affected by a pretreatment with L-arginine methyl ester, tetraethylammonium, or 4-aminopyridine. Pinacidil also inhibited the acetylcholine (ACh)-induced tonic and phasic contractions in a glibenclamide-sensitive manner (42% and 6% of the control, respectively). Other K<sub>ATP</sub> channel openers such as diazoxide, cromakalim and nicorandil also inhibited the spontaneous and ACh-induced contractions. Calcitonin gene-related peptide (CGRP), a gastric neuropeptide, induced muscle relaxation by the activation of K<sub>ATP</sub> channels in human gastric smooth muscle. Finally, we have found with Western blot studies, that human gastric smooth muscle expressed K<sub>ATP</sub> channels which were composed of Kir 6.2 and SUR2B subunits.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"56 0","pages":"29-45"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.56.29","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38081389","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Diagnosis and treatments for oropharyngeal dysphagia: effects of capsaicin evaluated by newly developed ultrasonographic method.","authors":"Rui Nakato, Noriaki Manabe, Kozo Hanayama, Hiroaki Kusunoki, Jiro Hata, Ken Haruma","doi":"10.1540/jsmr.56.46","DOIUrl":"https://doi.org/10.1540/jsmr.56.46","url":null,"abstract":"<p><p>Oropharyngeal dysphagia (OD) is a common symptom in the older people, and may cause fatal complications such as aspiration pneumonia. However, there is no established treatment for OD. The relationship between the transient receptor potential vanilloid 1 (TRPV1) and substance P released by activated TRPV1 was recently demonstrated. Further, there are several reports showing that capsaicin, a specific agonist of TRPV1, can improve OD. Currently, the evaluation of swallowing is mainly performed by videofluoroscopic examination. However, there are no reports on the clinical application of ultrasonography using tissue Doppler imaging. In this review, we describe the pathophysiology and treatments for OD, introduce our novel US method to evaluate cervical esophageal motility, and then outline our clinical study examining the effects of capsaicin, a specific TRPV1 agonist, in older patients with OD.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"56 0","pages":"46-57"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7324726/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38081391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"The inhibitory effect of somatostatin on gastric motility in Suncus murinus.","authors":"Haruka Sekiya, Naho Yokota, Shota Takemi, Keiji Nakayama, Hiroki Okada, Takafumi Sakai, Ichiro Sakata","doi":"10.1540/jsmr.56.69","DOIUrl":"https://doi.org/10.1540/jsmr.56.69","url":null,"abstract":"<p><p>Gastric contractions show two specific patterns in many species, migrating motor contractions (MMC) and postprandial contractions (PPCs), that occur in the fasted and fed states, respectively. In this study, we examined the role of somatostatin (SST) in gastric motility both in vivo and in vitro using the Asian house shrew (Suncus murinus). We performed in vivo recordings of gastric motility and in vitro organ bath experiments using S. murinus, which was recently established as a small laboratory animal for use in tests of gastrointestinal motility. SST (1.65 µg kg<sup>-1</sup> min<sup>-1</sup>) was intravenously administered during phase II of MMC and PPCs. Next, the effect of SST on motilin-induced gastric contractions at phase I of MMC was measured. Cyclosomatostatin (CSST), an SST receptor antagonist, was administered at the peak of phase III of MMC. In addition, the effect of SST (10<sup>-11</sup>-10<sup>-9</sup> M) on motilin-induced gastric contractions was evaluated using an organ bath experiment in vitro. In conscious, free-moving S. murinus, the administration of SST decreased the occurrence of the spontaneous phase II of MMC and PPCs. Pretreatment with SST and octreotide suppressed the induction of motilin-induced gastric contractions both in vivo and in vitro. Administration of CSST before the peak of spontaneous phase III contractions had no effect on gastric contractions. Endogenous SST is not involved in the regulation of gastric MMC and PPCs, but exogenous SST suppresses spontaneous gastric contractions. Thus, SST would be good for treating abnormal gastrointestinal motility disorders.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"56 0","pages":"69-81"},"PeriodicalIF":0.0,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/ae/4f/jsmr-56-069.PMC7817339.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38761996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Muscle cells, nerves, fibroblasts and vessels in the detrusor of the rat urinary bladder","authors":"G. Gabella","doi":"10.1540/jsmr.55.34","DOIUrl":"https://doi.org/10.1540/jsmr.55.34","url":null,"abstract":"All the cells of rat detrusor muscle fall into one of five ultrastructural types: muscle cells, fibroblasts, axons and glia, and vascular cells (endothelial cells and pericytes). The tissue is ~79% cellular and 21% non-cellular. Muscle cells occupy 72%, nerves ~4% (1/3 axons, 2/3 glia), and fibroblast >3% of space. Muscle cells (up to 6 µm across and ~600 µm long, packed to almost 100,000 per mm2) have surface-to-volume ratio of 2.4 µm2/µm3 ~93% of cell volume is contractile apparatus, 3.1% mitochondria and 2.5% nucleus. Cell profiles are irregular but sectional area decreases regularly towards either end of the cell. Muscle cells are gathered into bundles (the mechanical units of detrusor), variable in length and size, but of constant width. The musculature is highly compact (without fascia or capsule) with smooth outer surfaces and extensive association and adhesion between its cells. Among many types of intercellular contact and junction, digitations are very common, each muscle cell issuing minute finger-like processes that abut on adjacent cells. Sealed apposition are wide areas of specialized contact, possibly forming a chamber between two muscle cells, distinct from the extracellular space at large (stromal space). The innervation is very dense, virtually all intramuscular axons being varicose (including afferent ones). There are identifiable neuro-muscular junctions on each muscle cell, often several junctions on a single cell. There are also unattached terminals. Fibroblasts (involved in the production of collagen), ~1% of the total number of cells, do not make specialized contacts.","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 1","pages":"34 - 67"},"PeriodicalIF":0.0,"publicationDate":"2019-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.55.34","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45449328","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hanna Ługowska-Umer, A. Umer, K. Kuziemski, Łukasz Sein-Anand, R. Korolkiewicz
{"title":"The protective effect of endothelin receptor antagonists against surgically induced impairment of gastrointestinal motility in rats","authors":"Hanna Ługowska-Umer, A. Umer, K. Kuziemski, Łukasz Sein-Anand, R. Korolkiewicz","doi":"10.1540/jsmr.55.23","DOIUrl":"https://doi.org/10.1540/jsmr.55.23","url":null,"abstract":"Endothelin (ET) receptor antagonists: BQ-123 (ETA), BQ-788 (ETB), tezosentan (dual ET receptor antagonist) protect against the development of postoperative ileus (POI) evoked by ischemia-reperfusion (I/R). The current experiments explored whether ET antagonists prevent the occurrence of POI evoked by surgical gut manipulation. Intestinal transit was assessed by measuring the rate of dye migration subsequent to skin incision (SI), laparotomy (L), or laparotomy and surgical gut handling (L+M) in diethyl ether anaesthesized rats (E). Experimental animals were randomly sub-divided into two groups depending on the time of recovery following surgery: viz. either 2 or 24 h (early or late phase POI). E and SI did not affect the gastrointestinal (GI) transit. In contrast, L and L+M significantly reduced GI motility in comparison to untreated group (UN). Tezosentan (10 mg/kg), BQ-123 and BQ-788 (1 mg/kg) protected against development of L+M evoked inhibition of intestinal motility in the course of late phase, but not early phase POI. Furthermore, tezosentan alleviated the decrease in the contractile response of the longitudinal jejunal smooth muscle strips to carbachol in vitro induced by L+M. The serum ET(1–21) concentration was not increased in either the early or the late phase POI groups after surgery compared to control animals. This study indicates that delay in the intestinal transit in late phase of surgically induced POI involves an ET-dependent mechanism.","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 1","pages":"23 - 33"},"PeriodicalIF":0.0,"publicationDate":"2019-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.55.23","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47838889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Sustained exposure to prostaglandin D<sub>2</sub> augments the contraction induced by acetylcholine via a DP<sub>1</sub> receptor-mediated activation of p38 in bronchial smooth muscle of naive mice.","authors":"Wataru Suto, Hiroyasu Sakai, Yoshihiko Chiba","doi":"10.1540/jsmr.55.1","DOIUrl":"https://doi.org/10.1540/jsmr.55.1","url":null,"abstract":"<p><p>Prostaglandin D<sub>2</sub> (PGD<sub>2</sub>), one of the key lipid mediators of allergic airway inflammation, is increased in the airways of asthmatics. However, the role of PGD<sub>2</sub> in the pathogenesis of asthma is not fully understood. In the present study, effects of PGD<sub>2</sub> on smooth muscle contractility of the airways were determined to elucidate its role in the development of airway hyperresponsiveness (AHR). In a murine model of allergic asthma, antigen challenge to the sensitized animals caused a sustained increase in PGD<sub>2</sub> levels in bronchoalveolar lavage (BAL) fluids, indicating that smooth muscle cells of the airways are continually exposed to PGD<sub>2</sub> after the antigen exposure. In bronchial smooth muscles (BSMs) isolated from naive mice, a prolonged incubation with PGD<sub>2</sub> (10<sup>-5</sup> M, for 24 h) induced an augmentation of contraction induced by acetylcholine (ACh): the ACh concentration-response curve was significantly shifted upward by the 24-h incubation with PGD<sub>2</sub>. Application of PGD<sub>2</sub> caused phosphorylation of ERK1/2 and p38 in cultured BSM cells: both of the PGD<sub>2</sub>-induced events were abolished by laropiprant (a DP<sub>1</sub> receptor antagonist) but not by fevipiprant (a DP<sub>2</sub> receptor antagonist). In addition, the BSM hyperresponsiveness to ACh induced by the 24-h incubation with PGD<sub>2</sub> was significantly inhibited by co-incubation with SB203580 (a p38 inhibitor), whereas U0126 (a ERK1/2 inhibitor) had no effect on it. These findings suggest that prolonged exposure to PGD<sub>2</sub> causes the BSM hyperresponsiveness via the DP<sub>1</sub> receptor-mediated activation of p38. A sustained increase in PGD<sub>2</sub> in the airways might be a cause of the AHR in allergic asthmatics.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 0","pages":"1-13"},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.55.1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37095819","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Recent advances in intestinal smooth muscle research: from muscle strips and single cells, via ICC networks to whole organ physiology and assessment of human gut motor dysfunction.","authors":"Jan D Huizinga","doi":"10.1540/jsmr.55.68","DOIUrl":"10.1540/jsmr.55.68","url":null,"abstract":"<p><p>Gastrointestinal smooth muscle research has evolved from studies on muscle strips to spatiotemporal mapping of whole organ motor and electrical activities. Decades of research on single muscle cells and small sections of isolated musculature from animal models has given us the groundwork for interpretation of human in vivo studies. Human gut motility studies have dramatically improved by high-resolution manometry and high-resolution electrophysiology. The details that emerge from spatiotemporal mapping of high-resolution data are now of such quality that hypotheses can be generated as to the physiology (in healthy subjects) and pathophysiology (in patients) of gastrointestinal (dys) motility. Such interpretation demands understanding of the musculature as a super-network of excitable cells (neurons, smooth muscle cells, other accessory cells) and oscillatory cells (the pacemaker interstitial cells of Cajal), for which mathematical modeling becomes essential. The developing deeper understanding of gastrointestinal motility will bring us soon to a level of precision in diagnosis of dysfunction that is far beyond what is currently available.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 0","pages":"68-80"},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/dd/20/jsmr-55-068.PMC6962316.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37559065","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Inhibitory effects of rubratoxin A, a potent inhibitor of protein phosphatase 2, on the Ca<sup>2+</sup>-dependent contraction of skinned carotid artery from guinea pig.","authors":"Yasuyuki Naraki, Masaru Watanabe, Kosuke Takeya","doi":"10.1540/jsmr.55.14","DOIUrl":"https://doi.org/10.1540/jsmr.55.14","url":null,"abstract":"<p><p>Rubratoxin A, a potent inhibitor of PP2A, is known to suppress smooth muscle contraction. The inhibitory role of PP2A in smooth muscle contraction is still unclear. In order to clarify the regulatory mechanisms of PP2A on vascular smooth muscle contractility, we examined the effects of rubratoxin A on the Ca<sup>2+</sup>-induced contraction of β-escin skinned carotid artery preparations from guinea pigs. Rubratoxin A at 1 µM and 10 µM significantly inhibited skinned carotid artery contraction at any Ca<sup>2+</sup> concentration. The data fitting to the Hill equation in [Ca<sup>2+</sup>]-contraction relationship indicated that rubratoxin A decreased F<sub>max-Ca2+</sub> and increased [Ca<sup>2+</sup>]<sub>50</sub>, indices of Ca<sup>2+</sup> sensitivity for the force and myosin-actin interaction, respectively. These results suggest that PP2A inhibition causes downregulation of the myosin light chain phosphorylation and direct interference with myosin-actin interaction.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 0","pages":"14-22"},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.55.14","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37170834","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Fumitake Usui-Kawanishi, Masafumi Takahashi, Hiroyasu Sakai, Wataru Suto, Yuki Kai, Yoshihiko Chiba, Keizo Hiraishi, Lin Hai Kurahara, Masatoshi Hori, Ryuji Inoue
{"title":"Implications of immune-inflammatory responses in smooth muscle dysfunction and disease.","authors":"Fumitake Usui-Kawanishi, Masafumi Takahashi, Hiroyasu Sakai, Wataru Suto, Yuki Kai, Yoshihiko Chiba, Keizo Hiraishi, Lin Hai Kurahara, Masatoshi Hori, Ryuji Inoue","doi":"10.1540/jsmr.55.81","DOIUrl":"https://doi.org/10.1540/jsmr.55.81","url":null,"abstract":"<p><p>In the past few decades, solid evidence has been accumulated for the pivotal significance of immunoinflammatory processes in the initiation, progression, and exacerbation of many diseases and disorders. This groundbreaking view came from original works by Ross who first described that excessive inflammatory-fibroproliferative response to various forms of insult to the endothelium and smooth muscle of the artery wall is essential for the pathogenesis of atherosclerosis (Ross, Nature 1993; 362(6423): 801-9). It is now widely recognized that both innate and adaptive immune reactions are avidly involved in the inflammation-related remodeling of many tissues and organs. When this state persists, irreversible fibrogenic changes would occur often culminating in fatal insufficiencies of many vital parenchymal organs such as liver, lung, heart, kidney and intestines. Thus, inflammatory diseases are becoming the common life-threatening risk for and urgent concern about the public health in developed countries (Wynn et al., Nature Medicine 2012; 18(7): 1028-40). Considering this timeliness, we organized a special symposium entitled \"Implications of immune/inflammatory responses in smooth muscle dysfunction and disease\" in the 58th annual meeting of the Japan Society of Smooth Muscle Research. This symposium report will provide detailed synopses of topics presented in this symposium; (1) the role of inflammasome in atherosclerosis and abdominal aortic aneurysms by Fumitake Usui-Kawanishi and Masafumi Takahashi; (2) Mechanisms underlying the pathogenesis of hyper-contractility of bronchial smooth muscle in allergic asthma by Hiroyasu Sakai, Wataru Suto, Yuki Kai and Yoshihiko Chiba; (3) Vascular remodeling in pulmonary arterial hypertension by Keizo Hiraishi, Lin Hai Kurahara and Ryuji Inoue.</p>","PeriodicalId":39619,"journal":{"name":"Journal of Smooth Muscle Research","volume":"55 0","pages":"81-107"},"PeriodicalIF":0.0,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1540/jsmr.55.81","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"37613602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}