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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="publisher-id">853012</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2022.853012</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Application of Traditional Japanese Drug Jidabokuippo in a Modern Society</article-title>
<alt-title alt-title-type="left-running-head">Nakae et al.</alt-title>
<alt-title alt-title-type="right-running-head">Application of Jidabokuippo</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name>
<surname>Nakae</surname>
<given-names>Hajime</given-names>
</name>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<uri xlink:href="https://loop.frontiersin.org/people/541251/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Irie</surname>
<given-names>Yasuhito</given-names>
</name>
<uri xlink:href="https://loop.frontiersin.org/people/1295274/overview"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kitamura</surname>
<given-names>Toshiharu</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Okuyama</surname>
<given-names>Manabu</given-names>
</name>
</contrib>
</contrib-group>
<aff>
<institution>Department of Emergency and Critical Care Medicine</institution>, <institution>Akita University Graduate School of Medicine</institution>, <addr-line>Akita</addr-line>, <country>Japan</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/753899/overview">Kenny Kuchta</ext-link>, University Medical Center G&#xf6;ttingen, Germany</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/264459/overview">Masahiro Ohsawa</ext-link>, Nagoya City University, Japan</p>
<p>
<ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/158688/overview">Satoshi Iwase</ext-link>, Aichi Medical University, Japan</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Hajime Nakae, <email>nakaeh@doc.med.akita-u.ac.jp</email>
</corresp>
<fn fn-type="other">
<p>This article was submitted to Ethnopharmacology, a section of the journal Frontiers in Pharmacology</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>23</day>
<month>05</month>
<year>2022</year>
</pub-date>
<pub-date pub-type="collection">
<year>2022</year>
</pub-date>
<volume>13</volume>
<elocation-id>853012</elocation-id>
<history>
<date date-type="received">
<day>12</day>
<month>01</month>
<year>2022</year>
</date>
<date date-type="accepted">
<day>11</day>
<month>04</month>
<year>2022</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2022 Nakae, Irie, Kitamura and Okuyama.</copyright-statement>
<copyright-year>2022</copyright-year>
<copyright-holder>Nakae, Irie, Kitamura and Okuyama</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>
<bold>Background:</bold> Jidabokuippo (JDI) (&#x6cbb;&#x6253;&#x64b2;&#x4e00;&#x65b9;) has been used in Japan to alleviate contusion-induced swelling and pain since medieval times.</p>
<p>
<bold>Method:</bold> This review investigated the effects of JDI on various symptoms in patients with trauma or static blood<sup>[TM1]</sup>. The PubMed and Igaku Chuo Zasshi databases were searched until 24 December 2021. We summarize the benefits of applying JDI to inflammatory conditions, including bruises.</p>
<p>
<bold>Results:</bold> JDI has been used to resolve blood <sup>[TM1]</sup> stasis, regulate qi in trauma patients, and treat inflammatory swelling and pain caused by rheumatoid arthritis and cellulitis. As the adverse event rate associated with JDI is low (1.3%), JDI is considered a safe drug.</p>
<p>
<bold>Conclusion:</bold> JDI can be used to resolve blood<sup>[TM1]</sup> stasis in trauma patients without adverse events associated with nonsteroidal anti-inflammatory drugs.</p>
</abstract>
<kwd-group>
<kwd>trauma</kwd>
<kwd>inflammatory swelling</kwd>
<kwd>made-in-Japan</kwd>
<kwd>static blood</kwd>
<kwd>adverse event</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p>Jidabokuippo (JDI) (&#x6cbb;&#x6253;&#x64b2;&#x4e00;&#x65b9;) is an herbal mixture used in Japan to alleviate contusion-induced swelling and pain. It is composed of <italic>Nuphar japonica</italic> DC., <italic>Quercus acutissima</italic> Carruth., <italic>Ligusticum officinale</italic> (Makino) Kitag., <italic>Neolitsea cassia</italic> (L.) Kosterm., <italic>Syzygium aromaticum</italic> (L.) Merr. and L.M.Perry, <italic>Rheum palmatum</italic> L., and <italic>Glycyrrhiza glabra</italic> L. (<xref ref-type="table" rid="T1">Table 1</xref>; <xref ref-type="fig" rid="F1">Figure 1</xref>) (Department of Pharmacognosy and DPPN, 2018; <xref ref-type="bibr" rid="B53">Sakakibara, 2008</xref>; <xref ref-type="bibr" rid="B40">Nakae and Irie, 2020</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>Pharmacological action of formulated crude drugs in jidabokuippo.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Crude drug</th>
<th align="center">Composition ratio (g)</th>
<th align="center">Efficacy in Kampo medicine</th>
<th align="center">Pharmacological action</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">
<italic>Nuphar japonica</italic> DC.</td>
<td align="char" char=".">3.0</td>
<td align="left">Resolving blood<sup>[TM1]</sup> stasis and stomachic property</td>
<td align="left">Analgesia, diuresis, and anti-edematous action</td>
</tr>
<tr>
<td align="left">
<italic>Quercus acutissima</italic> Carruth</td>
<td align="char" char=".">3.0</td>
<td align="left">Resolving blood<sup>[TM1]</sup> stasis and antidiarrheal action</td>
<td align="left">Boosting and convergence</td>
</tr>
<tr>
<td align="left">
<italic>Ligusticum officinale</italic> (Makino) Kitag</td>
<td align="char" char=".">3.0</td>
<td align="left">Resolving blood<sup>[TM1]</sup> stasis, regulating qi, removing wind<sup>[TM1]</sup> and dampness<sup>[TM1]</sup>, and pain-relieving</td>
<td align="left">Central inhibition, telangiectasia, antithrombotic action, spasmolytic, increasing action on digestive tract mucosa blood flow volume, the elevation of skin temperature, and immunostimulation</td>
</tr>
<tr>
<td align="left">
<italic>Neolitsea cassia</italic> (L.) Kosterm</td>
<td align="char" char=".">3.0</td>
<td align="left">Releasing exterior, descending qi, resolving blood<sup>[TM1]</sup> stasis, pain-relieving</td>
<td align="left">Perspiration and antipyretic, sedation and spasmolytic, telangiectasia, decreasing blood pressure, antithrombotic action, anti-inflammation, antibacterial action, antitumor action, and regulation of water metabolism</td>
</tr>
<tr>
<td align="left">
<italic>Syzygium aromaticum</italic> (L.) Merr. and L.M.Perry</td>
<td align="char" char=".">1.0</td>
<td align="left">Warming spleen<sup>[TM1]</sup>, stomach<sup>[TM1]</sup>, and kidney<sup>[TM1]</sup>, and descending qi counterflow</td>
<td align="left">Anti-inflammatory, antibacterial action, antiviral action, sedation, and spasmolytic</td>
</tr>
<tr>
<td align="left">
<italic>Rheum palmatum</italic> L</td>
<td align="char" char=".">1.0</td>
<td align="left">Purgative, heat<sup>[TM1]</sup>-clearing, and resolving blood<sup>[TM1]</sup> stasis</td>
<td align="left">Catharsis, antibacterial action, psychotropic, anti-inflammatory, immunostimulation, lipid metabolism, and antithrombotic action</td>
</tr>
<tr>
<td align="left">
<italic>Glycyrrhiza glabra</italic> L</td>
<td align="char" char=".">1.5</td>
<td align="left">Descending qi, sedative action, relaxing tensions, pain-relieving, warming, and tonifying action, relieving purgative action, preserving fluid<sup>[TM1]</sup>, and stomachic property</td>
<td align="left">Sedation and spasmolytic, antitussive action, anti-inflammatory, antitumor action, antibacterial action, and antiviral action</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>TM1: traditional medicine module 1</p>
</fn>
</table-wrap-foot>
</table-wrap>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>Three-dimensional high-performance liquid chromatography profile of jidabokuippo. <italic>Nuphar japonica</italic> DC. contains major ingredients: nupharidine, deoxynupharidine, nupharamine, and nupharin. <italic>Quercus acutissima</italic> Carruth. contains quercitrin, scopoline, fraxin, and tannic acid. <italic>Ligusticum officinale</italic> (Makino) Kitag. contains cnidilide, neocnidilide, ligustilide&#x2a;, senkyunolide&#x2a;, butylphthalide, butylidenephthalide, pregnenolone, vanillin, coniferyl ferulate, ferulic acid, and scopoletin. <italic>Neolitsea cassia</italic> (L.) Kosterm. contains cinnamaldehyde&#x2a;, cinnamyl acetate, phenylpropyl acetate, cinnamic acid&#x2a;, and salicylaldehyde. <italic>Syzygium aromaticum</italic> (L.) Merr. and L.M.Perry contains acetyleugenol, chavicol, caryophyllene, humulene, caryophylla, eugenocide, eugeniin, higenamine, rhamnetin, and kaempferol. <italic>Rheum palmatum</italic> L. contains sennoside A&#x2a;&#x2013;F, rhein&#x2a;, aloe emodin&#x2a;, emodin&#x2a;, chrysophanol&#x2a;, naphthalene, catechin&#x2a;, epicatechin, and cinnamic acid&#x2a;. <italic>Glycyrrhiza glabra</italic> L. contains glycyrrhizin&#x2a;, glabric acid, liquiritin&#x2a;, liquiritin apioside&#x2a;, liquiritigenin&#x2a;, isoliquiritin&#x2a;, licoricidin, licoricone, licoflavone, formononetin&#x2a;, glycerol, and glycycoumarin&#x2a;.&#x2a;Shown in Panel 1).</p>
</caption>
<graphic xlink:href="fphar-13-853012-g001.tif"/>
</fig>
<p>Herein, we document that JDI treatments have been applied to bruises and various inflammation conditions since medieval Japanese society. Potentially relevant articles were identified through a PubMed and Igaku Chuo Zasshi (ICHUSHI) literature search using the keywords (jidabokuppo OR jidabokuippou) for articles published until 24 December 2021. ICHUSHI contains bibliographic citations and abstracts from more than 2,500 biomedical journals and other serial publications published in Japan. Since Kampo medicine targets many intractable and rare diseases and the course of treatment differs in each case, it is difficult to conduct large-scale randomized controlled trials and secure high-quality evidence. Therefore, a case report and case series are also included.</p>
</sec>
<sec id="s2">
<title>Source</title>
<p>Kampo prescriptions developed by Japanese expert clinicians in the Edo era were called &#x201c;honchokeikenho&#x201d; and are thought to include JDI. In the Sengoku era, the age of provincial wars (1467&#x2013;1615), some traumatologists called &#x201c;kinsoi&#x201d; used drugs that resembled JDI for sword wounds. Shuan Kagawa, who lived from 1683 to 1755, finalized JDI and collected information on treating bruises. It was originally named &#x201c;ippo (&#x4e00;&#x65b9;)&#x201d; for &#x201c;bruise&#x201d; in &#x201c;Ippondo-iji-setsuyaku.&#x201d; Sohaku Asada, a well-known Kampo medicine expert who practiced during the late 19th century (between the end of the Edo era and the early Meiji era), was the first to call it JDI in &#x201c;Futsugo-yakushitsu-hokan-kuketsu&#x201d; published in 1878. He reported that Shuan Kagawa developed JDI (<xref ref-type="bibr" rid="B3">Asada, 1981</xref>; <xref ref-type="bibr" rid="B26">Morikubo, 1999</xref>; <xref ref-type="bibr" rid="B40">Nakae and Irie, 2020</xref>).</p>
</sec>
<sec id="s3">
<title>Application of Jidabokuippo in the Classical Period</title>
<p>Shuan Kagawa reported that <italic>Quercus</italic> bark has the potential to resolve blood<sup>[TM1]</sup> stasis and improve fluid congestion found in bruises in &#x201c;Ippondoyakusen (<xref ref-type="bibr" rid="B15">Ippondoyakusen, 2021</xref>).&#x201d; Contusion and pain caused by trauma are considered static blood<sup>[TM1]</sup>, a sign of a microcirculatory disorder, and JDI alleviates blood<sup>[TM1]</sup> stasis patterns (<xref ref-type="bibr" rid="B26">Morikubo, 1999</xref>). Gentatsu Matsuoka, who lived from 1668 to 1746, reported that <italic>Nuphar japonica</italic> should be used for bruises. Prescriptions that included it were especially effective for bruises in &#x201c;Yoyakusuchi (<xref ref-type="bibr" rid="B83">Yoyakusuchi, 2021</xref>).&#x201d; Sohaku Asada explained that JDI improved myalgia and ostealgia caused by trauma; <italic>Nuphar japonica</italic> improved blood flow, and <italic>Quercus acutissima</italic> alleviated ostealgia. These two crude elements were the principal agents. <italic>Aconitum carmichaelii</italic> Debeaux with warm meridian is added in the chronic stage in &#x201c;Futsugo-yakushitsu-hokan-kuketsu&#x201d; (<xref ref-type="bibr" rid="B3">Asada, 1981</xref>). He also explained that dokoppito (&#x571f;&#x9aa8;&#x76ae;&#x6e6f;), composed of <italic>Quercus acutissima</italic>, <italic>Carthamus tinctorius</italic> L., <italic>Glycyrrhiza glabra</italic>, <italic>Bupleurum falcatum</italic> L., and <italic>Curcuma zedoaria</italic> (Christm.) Roscoe improved eczema capitis and ostealgia. In dokoppi, also known as Bokusoku, <italic>Quercus acutissima</italic> has strong potential of releasing exterior in &#x201c;Futsugo-yakushitsu-hokan-kuketsu.&#x201d;</p>
<p>
<italic>Rheum palmatum</italic> has sedative effects in addition to resolving blood<sup>[TM1]</sup> stasis (<xref ref-type="bibr" rid="B60">Sumida et al., 1988</xref>). <italic>Ligusticum officinale</italic>, <italic>Neolitsea cassia</italic>, and <italic>Syzygium aromaticum</italic> have the potential to regulate qi (<xref ref-type="table" rid="T1">Table 1</xref>). Wada Tokaku, who lived from 1742 to 1803, stated &#x201c;It is not good resolving blood<sup>[TM1]</sup> stasis using <italic>Carthamus tinctorius</italic> and <italic>Biancaea sappan</italic> (L.) Tod. for bruises. The regulating qi method should be chosen for this purpose. Provide sedation using shigyakusan (&#x56db;&#x9006;&#x6563;) or jinkokokito (&#x6c88;&#x9999;&#x964d;&#x6c17;&#x6e6f;)&#x201d; (<xref ref-type="bibr" rid="B57">Shosozatsuwa, 2021</xref>). Since both resolving blood<sup>[TM1]</sup> stasis and regulating qi should be performed for the treatment of bruises, JDI is thought to have the ideal composition of crude drugs.</p>
<p>Kampo formulations are made from several crude drugs, with each crude drug having several constituents. Therefore, Kampo prescriptions are considered interaction-based multicomponent medicines. The blending effect of crude drugs in JDI is shown in <xref ref-type="table" rid="T2">Table 2</xref>.</p>
<table-wrap id="T2" position="float">
<label>TABLE 2</label>
<caption>
<p>Blending effect of formulated crude drugs in jidabokuippo.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Blended crude drug</th>
<th align="center">Efficacy in Kampo medicine</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">
<italic>Nuphar japonica</italic> &#x2b; <italic>Ligusticum officinale</italic>
</td>
<td align="left">Reducing fluid congestion in a bruise and relieving pain</td>
</tr>
<tr>
<td align="left">
<italic>Quercus acutissima</italic> &#x2b; <italic>Ligusticum officinale</italic>
</td>
<td align="left">Resolving blood<sup>[TM1]</sup> stasis, healing bruise, wound, and hematoma</td>
</tr>
<tr>
<td align="left">
<italic>Quercus acutissima</italic> &#x2b; <italic>Nuphar japonica</italic>
</td>
<td align="left">Improving blood circulation and relieving pain in blood<sup>[TM1]</sup> stasis</td>
</tr>
<tr>
<td align="left">
<italic>Quercus acutissima</italic> &#x2b; <italic>Rheum palmatum</italic>
</td>
<td align="left">Clearing heat<sup>[TM1]</sup> and resolving blood<sup>[TM1]</sup> stasis</td>
</tr>
<tr>
<td align="left">
<italic>Syzygium aromaticum</italic> &#x2b; <italic>Neolitsea cassia</italic>
</td>
<td align="left">Warming and improving blood circulation and healing congestive disease</td>
</tr>
<tr>
<td align="left">
<italic>Neolitsea cassia</italic> &#x2b; <italic>Glycyrrhiza glabra</italic>
</td>
<td align="left">Descending qi counterflow and tranquilization</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>TM1: traditional medicine module 1</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s4">
<title>Application of Jidabokuippo in the Modern Period</title>
<p>The relevance of JDI in modern society is the same as that in its classical use. In short, swelling caused by trauma is diagnosed as blood<sup>[TM1]</sup> stasis, and JDI is applied to resolve it (<xref ref-type="table" rid="T3">Table 3</xref>) (<xref ref-type="bibr" rid="B75">Yamamoto, 1975</xref>; <xref ref-type="bibr" rid="B9">Hijikata et al., 2007</xref>; <xref ref-type="bibr" rid="B7">Futenma et al., 2014</xref>; <xref ref-type="bibr" rid="B16">Irie and Nakae, 2019</xref>; <xref ref-type="bibr" rid="B81">Yoshinaga et al., 2020</xref>).</p>
<table-wrap id="T3" position="float">
<label>TABLE 3</label>
<caption>
<p>Previous reports of more than 10 cases using jidabokuippo.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">No.</th>
<th align="center">References</th>
<th align="center">Study design</th>
<th align="center">Injuries and diseases</th>
<th align="center">Number of cases</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">1</td>
<td align="left">
<xref ref-type="bibr" rid="B12">Ikeda et al. (1986)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Trauma</td>
<td align="center">109</td>
</tr>
<tr>
<td align="left">2</td>
<td align="left">
<xref ref-type="bibr" rid="B19">Kita et al. (1995)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Rheumatoid arthritis</td>
<td align="center">12</td>
</tr>
<tr>
<td align="left">3</td>
<td align="left">
<xref ref-type="bibr" rid="B64">Takagi (1995)</xref>
</td>
<td align="left">Cohort study</td>
<td align="left">Chronic pain caused by trauma</td>
<td align="center">18</td>
</tr>
<tr>
<td align="left">4</td>
<td align="left">
<xref ref-type="bibr" rid="B59">Sudo and Oribe (2005)</xref>
</td>
<td align="left">Cohort study</td>
<td align="left">Chronic pain caused by trauma</td>
<td align="center">23</td>
</tr>
<tr>
<td align="left">5</td>
<td align="left">
<xref ref-type="bibr" rid="B58">Sudo (2005)</xref>
</td>
<td align="left">Cross-sectional study</td>
<td align="left">Spinal compression fracture</td>
<td align="center">24</td>
</tr>
<tr>
<td align="left">6</td>
<td align="left">
<xref ref-type="bibr" rid="B54">Sakurai et al. (2006)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Facial injuries</td>
<td align="center">13</td>
</tr>
<tr>
<td align="left">7</td>
<td align="left">
<xref ref-type="bibr" rid="B66">Takeda (2010)</xref>
</td>
<td align="left">Randomized controlled study</td>
<td align="left">Anterior tibiofibular ligament injury</td>
<td align="center">17</td>
</tr>
<tr>
<td align="left">8</td>
<td align="left">
<xref ref-type="bibr" rid="B29">Nakae et al. (2012)</xref>
</td>
<td align="left">Randomized controlled study</td>
<td align="left">Rib fractures</td>
<td align="center">76</td>
</tr>
<tr>
<td align="left">9</td>
<td align="left">
<xref ref-type="bibr" rid="B25">Minamitani (2014)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Fractures and severe contusions</td>
<td align="center">10</td>
</tr>
<tr>
<td align="left">10</td>
<td align="left">
<xref ref-type="bibr" rid="B43">Nakae et al. (2015b)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Fractures of extremities</td>
<td align="center">50</td>
</tr>
<tr>
<td align="left">11</td>
<td align="left">
<xref ref-type="bibr" rid="B79">Yoshida (2015)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Facial contusions</td>
<td align="center">47</td>
</tr>
<tr>
<td align="left">12</td>
<td align="left">
<xref ref-type="bibr" rid="B38">Nakae et al. (2016)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Trauma</td>
<td align="center">643</td>
</tr>
<tr>
<td align="left">13</td>
<td align="left">
<xref ref-type="bibr" rid="B8">Hasegawa et al. (2016)</xref>
</td>
<td align="left">Cohort study</td>
<td align="left">Trauma/postoperative swelling</td>
<td align="center">53</td>
</tr>
<tr>
<td align="left">14</td>
<td align="left">
<xref ref-type="bibr" rid="B62">Suzuki and Yoshida (2016)</xref>
</td>
<td align="left">Cross-sectional study</td>
<td align="left">Postoperative finger swelling</td>
<td align="center">112</td>
</tr>
<tr>
<td align="left">15</td>
<td align="left">
<xref ref-type="bibr" rid="B52">Saito et al. (2019)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Obstetrics and gynecology patients</td>
<td align="center">112</td>
</tr>
<tr>
<td align="left">16</td>
<td align="left">
<xref ref-type="bibr" rid="B1">Akiyama et al. (2020)</xref>
</td>
<td align="left">Case series</td>
<td align="left">Head injury</td>
<td align="center">18</td>
</tr>
<tr>
<td align="left">17</td>
<td align="left">
<xref ref-type="bibr" rid="B20">Kitamura et al. (2022)</xref>
</td>
<td align="left">Cross-sectional study</td>
<td align="left">Trauma/postoperation</td>
<td align="center">1,104</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Yamamoto reported that JDI was effective for bruises in acute and chronic settings. JDI was much more effective than keishibukuryogan (&#x6842;&#x679d;&#x832f;&#x82d3;&#x4e38;), and aconite tuber should be added to JDI in the chronic stage. He also recommended treatment-induced diarrhea using JDI and <italic>Rheum palmatum</italic> in acute severely injured patients, regardless of stool consistency (<xref ref-type="bibr" rid="B75">Yamamoto, 1975</xref>).</p>
<p>Plants contain various antioxidants that protect organisms from injury caused by ultraviolet radiation. Kampo formulations have antioxidant and multiple bioactive properties (<xref ref-type="table" rid="T1">Table 1</xref>) (<xref ref-type="bibr" rid="B34">Nakae, 2011</xref>; <xref ref-type="bibr" rid="B11">Hirayama et al., 2018</xref>). Yamane evaluated the radical scavenging potentials of seven herbs [<italic>Rheum palmatum</italic>, <italic>Uncaria gambir</italic> (W.Hunter) Roxb., <italic>Syzygium aromaticum</italic>, <italic>Paeonia lactiflora</italic> Pallas, <italic>Glycyrrhiza glabra</italic>, <italic>Polyporus umbellatus</italic> Fries, and <italic>Prunus persica</italic> (L.) Batsch] and reported that the scavenging potential of diphenylpicrylhydrazyl (DPPH) was the highest in <italic>Rheum palmatum</italic>, followed by <italic>Syzygium aromaticum</italic> (<xref ref-type="bibr" rid="B76">Yamane et al., 2000</xref>). Tani suggested that polyphenol is closely involved in antioxidant effects based on a positive correlation between the polyphenol content and DPPH radical scavenging potential of herbs (<xref ref-type="bibr" rid="B67">Tani et al., 2004</xref>). They investigated 25 herbs. The polyphenol content was highest in <italic>Rheum palmatum</italic>, followed by <italic>Quercus acutissima</italic>, <italic>Nuphar japonica</italic>, <italic>Glycyrrhiza glabra</italic>, <italic>Syzygium aromaticum</italic>, and <italic>Neolitsea cassia</italic>. The DPPH radical scavenging potential was high in <italic>Rheum palmatum</italic>, followed by <italic>Quercus acutissima</italic>, <italic>Nuphar japonica</italic>, <italic>Syzygium aromaticum</italic>, and <italic>Neolitsea cassia</italic>. In addition, <italic>Ligusticum officinale</italic> have anti-inflammatory and antioxidant effects. A study designed to evaluate the effect of herbal extracts in suppressing reactive oxygen formation in human neutrophils showed a suppressive action by <italic>Ligusticum officinale</italic> (<xref ref-type="bibr" rid="B23">Luo et al., 1993</xref>). In addition, this herb protects organisms from radiation-induced damage (<xref ref-type="bibr" rid="B49">Ohta et al., 1987</xref>; <xref ref-type="bibr" rid="B56">Shinoda, 1995</xref>) and protects against edema (<xref ref-type="bibr" rid="B63">Tahara et al., 1998</xref>). <italic>Neolitsea cassia</italic> suppresses the formation of reactive oxygen in aqueous extracts (<xref ref-type="bibr" rid="B69">Toda et al., 1991</xref>), inhibits O<sub>2</sub> formation in macrophages (<xref ref-type="bibr" rid="B14">Imamichi et al., 1990</xref>), and protects against radiation disorders (<xref ref-type="bibr" rid="B49">Ohta et al., 1987</xref>). <italic>Rheum palmatum</italic>, containing anthraquinones, suppresses lipid peroxide formation in human neutrophils (<xref ref-type="bibr" rid="B24">Mian et al., 1987</xref>), and condensed tannins have radical scavenging activity (<xref ref-type="bibr" rid="B71">Uchida et al., 1988</xref>). <italic>Glycyrrhiza glabra</italic> has anti-inflammatory and edema-suppressing activities (<xref ref-type="bibr" rid="B22">Kumagai, 1982</xref>; <xref ref-type="bibr" rid="B2">Amagaya et al., 1984</xref>). In addition, <italic>Glycyrrhiza glabra</italic> protects organisms from radiation (<xref ref-type="bibr" rid="B49">Ohta et al., 1987</xref>). Thus, JDI includes herbs with antioxidant effects; these herbs may act synergistically to exert antioxidant effects.</p>
<p>We have previously demonstrated the antioxidant activity of JDI in a clinical setting (<xref ref-type="bibr" rid="B31">Nakae, 2010a</xref>). Swelling related to trauma occurs due to the enhanced permeability caused by the overproduction of chemical mediators such as free radicals. JDI may improve the pathological condition through these antioxidant properties.</p>
<p>In the clinical setting, Kampo prescriptions should be first administered in doses two to three times greater than the common starting doses in patients with severe symptoms (<xref ref-type="bibr" rid="B40">Nakae and Irie, 2020</xref>; <xref ref-type="bibr" rid="B42">Nakae et al., 2021</xref>).</p>
<p>The hypothetical mechanisms of JDI are shown in <xref ref-type="fig" rid="F2">Figure 2</xref>. A patient&#x2019;s signs and symptoms are diagnosed based on theories of Kampo medicine such as yin and yang, deficiency and excess, cold<sup>[TM1]</sup> and heat<sup>[TM1]</sup>, exterior<sup>[TM1]</sup> and interior<sup>[TM1]</sup>, six-stage patterns, qi, blood<sup>[TM1]</sup>, fluid<sup>[TM1]</sup>, and zang-fu organs. The patient is to be treated based on those patterns. When a patient&#x2019;s pattern is in static blood<sup>[TM1]</sup> and qi depression, JDI is applied to the pattern, regardless the patient&#x2019;s condition being acute or chronic inflammation.</p>
<fig id="F2" position="float">
<label>FIGURE 2</label>
<caption>
<p>Hypothetical mechanisms of jidabokuippo for acute and chronic inflammation.</p>
</caption>
<graphic xlink:href="fphar-13-853012-g002.tif"/>
</fig>
</sec>
<sec id="s5">
<title>Effectiveness of Jidabokuippo</title>
<p>As for the effectiveness of JDI as compared with Western drugs, there are only two randomized controlled studies (<xref ref-type="table" rid="T3">Table 3</xref>). Takeda compared the efficacy of JDI and nonsteroidal anti-inflammatory drugs (NSAIDs), loxoprofen, in patients with anterior tibiofibular ligament injuries by analyzing the treatment duration using a visual analog scale and girth <underline>(</underline>
<xref ref-type="bibr" rid="B66">Takeda, 2010</xref>). The results showed that compared to loxoprofen, JDI could shorten the swelling duration 2&#xa0;weeks after the administration. We compared the efficacy of JDI and NSAIDs in patients with rib fractures by analyzing the treatment duration. Our results suggest that compared to NSAIDs, JDI could shorten the treatment duration and may be a promising analgesic agent for both medical and economic reasons (<xref ref-type="bibr" rid="B29">Nakae et al., 2012</xref>.).</p>
<p>We have used JDI for various trauma such as rib fractures, fractures of extremities, abdominal wall hematoma, and traumatic asphyxia (<xref ref-type="bibr" rid="B29">Nakae et al., 2012</xref>; <xref ref-type="bibr" rid="B39">Nakae et al., 2015a</xref>; <xref ref-type="bibr" rid="B38">Nakae et al., 2016</xref>; <xref ref-type="bibr" rid="B20">Kitamura et al., 2022</xref>; <xref ref-type="bibr" rid="B43">Nakae et al., 2015b</xref>; <xref ref-type="bibr" rid="B41">Nakae et al., 2020</xref>.).</p>
<p>Suzuki reported that the JDI group had a significantly more robust remission effect than the non-JDI group in postoperative finger swelling (<xref ref-type="bibr" rid="B62">Suzuki and Yoshida, 2016</xref>). Nagashima reported that a 35-year-old man with massive subcutaneous swelling after decompressive craniectomy for head trauma showed a rapid reduction of swelling after JDI administration (<xref ref-type="bibr" rid="B27">Nagashima et al., 2018</xref>). Furthermore, JDI was applied for chronic subdural hematoma, puncture hematoma after angiography, and subgaleal hematoma with skull fractures (<xref ref-type="bibr" rid="B70">Tsugane et al., 2011</xref>; <xref ref-type="bibr" rid="B80">Yoshida et al., 2018</xref>; <xref ref-type="bibr" rid="B45">Nakao and Kaneko, 2019</xref>; <xref ref-type="bibr" rid="B74">Yamada et al., 2019</xref>). The use of JDI has also been applied to treat rheumatoid arthritis and cellulitis (<xref ref-type="bibr" rid="B19">Kita et al., 1995</xref>; <xref ref-type="bibr" rid="B47">Nogami et al., 2003</xref>; <xref ref-type="bibr" rid="B82">Yoshinaga et al., 2021</xref>). Since JDI has antioxidant activity and also inhibits prostaglandin production, its indications may be broader. In Kampo medicine, peripheral neuropathy is often diagnosed as related to blood<sup>[TM1]</sup> deficiency, static blood<sup>[TM1]</sup>, fluid<sup>[TM1]</sup> retention, and kidney<sup>[TM1]</sup> deficiency (<xref ref-type="bibr" rid="B55">Shimada, 2005</xref>). Therefore, JDI can resolve blood<sup>[TM1]</sup> stasis in these indications (<xref ref-type="bibr" rid="B72">Uemura et al., 2013</xref>; <xref ref-type="bibr" rid="B46">Narai et al., 2014</xref>; <xref ref-type="bibr" rid="B50">Okamoto, 2015</xref>; <xref ref-type="bibr" rid="B73">Yabe et al., 2018</xref>). Furthermore, JDI has been used for unexplained perineal pain and wasp stings (<xref ref-type="bibr" rid="B36">Nakae, 2013a</xref>; <xref ref-type="bibr" rid="B48">Ogata et al., 2019</xref>).</p>
<p>Concomitant use of NSAIDs or other Kampo medicines may be necessary for multiple injuries should severe inflammatory reactions occur and severe pain persist (<xref ref-type="table" rid="T4">Table 4</xref>) (<xref ref-type="bibr" rid="B78">Yonemitsu, 2017</xref>; <xref ref-type="bibr" rid="B17">Iwata, 2020</xref>). <italic>Aconitum carmichaelii</italic> should be added to JDI when swelling and pain persist. In Kampo medicine, <italic>Aconitum carmichaelii</italic> can move old blood<sup>[TM1]</sup> stasis (<xref ref-type="bibr" rid="B75">Yamamoto, 1975</xref>; <xref ref-type="bibr" rid="B65">Takamura et al., 2018</xref>). We previously reported that the <italic>Aconitum carmichaelii</italic> had analgesic and hyperthermic activity and increased blood flow (<xref ref-type="bibr" rid="B33">Nakae, 2008</xref>; <xref ref-type="bibr" rid="B28">Nakae et al., 2008</xref>; <xref ref-type="bibr" rid="B32">Nakae, 2010b</xref>; <xref ref-type="bibr" rid="B35">Nakae, 2010c</xref>; <xref ref-type="bibr" rid="B44">Nakae, 2010d</xref>; <xref ref-type="bibr" rid="B30">Nakae, 2013b</xref>; <xref ref-type="bibr" rid="B37">Nakae et al., 2014</xref>). Drug treatment with carbamazepine and pregabalin, nerve block injection, acupuncture, and moxibustion treatment combined with JDI were administered to treat neuropathic pain (<xref ref-type="bibr" rid="B18">Kase et al., 2009</xref>; <xref ref-type="bibr" rid="B13">Imaizumi et al., 2016</xref>; <xref ref-type="bibr" rid="B61">Suzuki et al., 2017</xref>; <xref ref-type="bibr" rid="B51">Okuno and Gi, 2019</xref>; <xref ref-type="bibr" rid="B77">Yano et al., 2020</xref>).</p>
<table-wrap id="T4" position="float">
<label>TABLE 4</label>
<caption>
<p>Concomitant use of Kampo medicine with jidabokuippo.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Kampo medicine</th>
<th align="center">The main potential in Kampo</th>
<th align="center">Knock-on effect of using</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">Keishibukuryogan</td>
<td rowspan="2" align="left">Resolving blood<sup>[TM1]</sup> stasis</td>
<td rowspan="2" align="left">No constipation</td>
</tr>
<tr>
<td align="left">&#x6842;&#x679d;&#x832f;&#x82d3;&#x4e38;</td>
</tr>
<tr>
<td align="left">&#x2003;Tsudosan</td>
<td rowspan="2" align="left">Resolving blood<sup>[TM1]</sup> stasis</td>
<td rowspan="2" align="left">Constipation</td>
</tr>
<tr>
<td align="left">&#x901a;&#x5c0e;&#x6563;</td>
</tr>
<tr>
<td align="left">&#x2003;Sokeikakketsuto</td>
<td rowspan="2" align="left">Regulating fluid<sup>[TM1]</sup>
</td>
<td rowspan="2" align="left">Chronic situation, numbness</td>
</tr>
<tr>
<td align="left">&#x758e;&#x7d4c;&#x6d3b;&#x8840;&#x6e6f;</td>
</tr>
<tr>
<td align="left">&#x2003;Goreisan</td>
<td rowspan="2" align="left">Regulating fluid<sup>[TM1]</sup>
</td>
<td rowspan="2" align="left">Head injury, whiplash injury (headache, nausea)<xref ref-type="table-fn" rid="Tfn1">
<sup>a</sup>
</xref>
</td>
</tr>
<tr>
<td align="left">&#x4e94;&#x82d3;&#x6563;</td>
</tr>
<tr>
<td align="left">&#x2003;Eppikajutsuto</td>
<td rowspan="2" align="left">Regulating fluid<sup>[TM1]</sup>
</td>
<td rowspan="2" align="left">Severe cellulitis</td>
</tr>
<tr>
<td align="left">&#x8d8a;&#x5a62;&#x52a0;&#x672e;&#x6e6f;</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>TM1: traditional medicine module 1</p>
</fn>
<fn id="Tfn1">
<label>a</label>
<p>Goreisan (&#x4e94;&#x82d3;&#x6563;) should be administered before jidabokuippo (&#x6cbb;&#x6253;&#x64b2;&#x4e00;&#x65b9;) use.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s6">
<title>A Possible Choice for Jidabokuippo</title>
<p>Takagi reported that JDI was effective in patients with abdominal tenderness at the right side of the paraumbilical site before treatment (<xref ref-type="fig" rid="F3">Figure 3</xref>) (<xref ref-type="bibr" rid="B64">Takagi, 1995</xref>). This tender point is considered to indicate blood<sup>[TM1]</sup> stasis (<xref ref-type="bibr" rid="B26">Morikubo, 1999</xref>; <xref ref-type="bibr" rid="B59">Sudo and Oribe, 2005</xref>; <xref ref-type="bibr" rid="B61">Suzuki et al., 2017</xref>). It is difficult to confirm whether Takagi&#x2019;s suggestion could be used in the absence of this tender point.</p>
<fig id="F3" position="float">
<label>FIGURE 3</label>
<caption>
<p>Tender point of jidabokuippo. When abdominal tenderness at the right side of the paraumbilical site was observed, JDI might have been effective.</p>
</caption>
<graphic xlink:href="fphar-13-853012-g003.tif"/>
</fig>
</sec>
<sec id="s7">
<title>Safety of Jidabokuippo</title>
<p>The incidence of adverse events associated with Kampo formulations remains unclear. Kitamura et al. studied the adverse events in 1,104 patients who had JDI prescribed (<xref ref-type="bibr" rid="B20">Kitamura et al., 2022</xref>). The reported adverse event rate was 1.3%, falling within a low rate of previous reports (0&#x2013;6.4%) (<xref ref-type="bibr" rid="B12">Ikeda et al., 1986</xref>; <xref ref-type="bibr" rid="B19">Kita et al., 1995</xref>; <xref ref-type="bibr" rid="B64">Takagi, 1995</xref>; <xref ref-type="bibr" rid="B59">Sudo and Oribe, 2005</xref>; <xref ref-type="bibr" rid="B58">Sudo, 2005</xref>; <xref ref-type="bibr" rid="B54">Sakurai et al., 2006</xref>; <xref ref-type="bibr" rid="B66">Takeda, 2010</xref>; <xref ref-type="bibr" rid="B29">Nakae et al., 2012</xref>; <xref ref-type="bibr" rid="B25">Minamitani, 2014</xref>; <xref ref-type="bibr" rid="B39">Nakae et al., 2015a</xref>; <xref ref-type="bibr" rid="B79">Yoshida, 2015</xref>; <xref ref-type="bibr" rid="B38">Nakae et al., 2016</xref>; <xref ref-type="bibr" rid="B8">Hasegawa et al., 2016</xref>; <xref ref-type="bibr" rid="B62">Suzuki and Yoshida, 2016</xref>; <xref ref-type="bibr" rid="B52">Saito et al., 2019</xref>; <xref ref-type="bibr" rid="B1">Akiyama et al., 2020</xref>). The most common adverse event was digestive symptoms (0.9%), with diarrhea caused by <italic>Rheum palmatum</italic> being the most common. The adverse event rate of glycyrrhiza-induced pseudoaldosteronism was 0.33% (<xref ref-type="table" rid="T5">Table 5</xref>). The adverse event rate associated with JDI use is low, and the onset is relatively rapid. Kon reported that the laxative action that accompanies decreased aquaporin-3 expression due to sennoside A in <italic>Rheum palmatum</italic> was mitigated by the anti-inflammatory effects of glycyrrhizin (<xref ref-type="bibr" rid="B21">Kon et al., 2018</xref>). Glycyrrhizin is considered to attenuate the adverse events caused by sennoside A. However, we need to pay attention to the pharmacological action of <italic>Rheum palmatum</italic> and <italic>Glycyrrhiza glabra</italic> before concluding that JDI is a safe drug.</p>
<table-wrap id="T5" position="float">
<label>TABLE 5</label>
<caption>
<p>Adverse events related to jidabokuippo.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th colspan="2" align="left">Adverse event</th>
<th align="center">Frequency<xref ref-type="table-fn" rid="Tfn2">
<sup>a</sup>
</xref>
</th>
<th align="center">Causative crude drugs</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td rowspan="4" align="left">Digestive symptom</td>
<td align="left">Diarrhea, loose stool, and abdominal pain</td>
<td align="center">0.47% (10/2,138)</td>
<td align="left">
<italic>Rheum palmatum</italic>
</td>
</tr>
<tr>
<td align="left">Nausea and vomiting</td>
<td align="center">0.28% (6/2,138)</td>
<td align="left">Combination of crude drugs</td>
</tr>
<tr>
<td align="left">Stomach heaviness</td>
<td align="center">0.09% (2/2,138)</td>
<td align="left">Combination of crude drugs</td>
</tr>
<tr>
<td align="left">Loss of appetite</td>
<td align="center">0.05% (1/2,138)</td>
<td align="left">Combination of crude drugs</td>
</tr>
<tr>
<td align="left">Pseudoaldosteronism</td>
<td align="left">Weight increase, edema, hypokalemia, and feeling of weakness</td>
<td align="center">0.33% (7/2,138)</td>
<td align="left">
<italic>Glycyrrhiza glabra</italic>
</td>
</tr>
<tr>
<td align="left">Skin symptom</td>
<td align="left">Rash</td>
<td align="center">0.09% (2/2,138)</td>
<td align="left">
<italic>Neolitsea cassia</italic>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn id="Tfn2">
<label>a</label>
<p>Calculated according to the previous reports (<xref ref-type="bibr" rid="B59">Sudo and Oribe, 2005</xref>; <xref ref-type="bibr" rid="B54">Sakurai et al., 2006</xref>; <xref ref-type="bibr" rid="B66">Takeda, 2010</xref>; <xref ref-type="bibr" rid="B29">Nakae et al., 2012</xref>; <xref ref-type="bibr" rid="B43">Nakae et al., 2015a</xref>; <xref ref-type="bibr" rid="B79">Yoshida, 2015</xref>; <xref ref-type="bibr" rid="B8">Hasegawa et al., 2016</xref>; <xref ref-type="bibr" rid="B38">Nakae et al., 2016</xref>; <xref ref-type="bibr" rid="B52">Saito et al., 2019</xref>; <xref ref-type="bibr" rid="B20">Kitamura et al., 2022</xref>).</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec sec-type="conclusion" id="s8">
<title>Conclusion</title>
<p>NSAIDs are often used to treat pain associated with trauma. However, NSAIDs intake often induces gastrointestinal symptoms. In addition, the use of selective cyclooxygenase-2 inhibitors poses a risk of ischemic heart disease (<xref ref-type="bibr" rid="B10">Hippisley-Cox and Coupland, 2005</xref>), and physicians hesitate to use them in patients with a history of cardiovascular disease. In recent years, proton pump inhibitors (PPIs) have been used to prevent NSAID-induced ulcers. However, PPIs pertain to medical economics, fractures, community-acquired pneumonia, watery stools, etc. (<xref ref-type="bibr" rid="B4">Bombardier et al., 2000</xref>; <xref ref-type="bibr" rid="B5">Dalton et al., 2009</xref>). JDI can be used as an alternative drug under such conditions. Moreover, JDI may be applied to non-trauma patients with blood<sup>[TM1]</sup> stasis. A large randomized controlled trial is necessary to establish JDI treatment for various diseases with blood<sup>[TM1]</sup> stasis.</p>
</sec>
</body>
<back>
<sec id="s9">
<title>Author Contributions</title>
<p>All authors contributed to the writing of this review. HN conceived the idea for the article, drafted the methods and results, and developed it in collaboration with YI, TK, and MO. HN wrote the first draft of the manuscript. YI and TK contributed to the article and edited the manuscript. All authors contributed to the revisions.</p>
</sec>
<sec sec-type="COI-statement" id="s10">
<title>Conflict of Interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="disclaimer" id="s11">
<title>Publisher&#x2019;s Note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<ack>
<p>The basic terms of Kampo medicine are based on the Dictionary of Kampo Medicine (Basic terms) of the Japanese Society of Oriental Medicine (<xref ref-type="bibr" rid="B68">The Editing Committee for Dictionary of Kampo Medicine, 2019</xref>). We acknowledge Editage (<ext-link ext-link-type="uri" xlink:href="https://www.editage.jp">https://www.editage.jp</ext-link>) for proofreading the text in English.</p>
</ack>
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