<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">NS</journal-id><journal-title-group><journal-title>Natural Science</journal-title></journal-title-group><issn pub-type="epub">2150-4091</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ns.2021.1310037</article-id><article-id pub-id-type="publisher-id">NS-112348</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Chemistry&amp;Materials Science</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  Biophoton Imaging Evaluation of the Process of Rheumatoid Arthritis in Rats
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Chengming</surname><given-names>Xia</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jinzhong</surname><given-names>Li</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yi</surname><given-names>Yue</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Linhua</surname><given-names>Chen</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jiapei</surname><given-names>Dai</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Wuhan Institute for Neuroscience and Neuroengineering (WINN), South-Central University for Nationalities, Wuhan, China</addr-line></aff><aff id="aff2"><addr-line>Department of Neurobiology, College of Life Sciences, South-Central University for Nationalities, Wuhan, China</addr-line></aff><pub-date pub-type="epub"><day>30</day><month>09</month><year>2021</year></pub-date><volume>13</volume><issue>10</issue><fpage>451</fpage><lpage>456</lpage><history><date date-type="received"><day>24,</day>	<month>August</month>	<year>2021</year></date><date date-type="rev-recd"><day>5,</day>	<month>October</month>	<year>2021</year>	</date><date date-type="accepted"><day>8,</day>	<month>October</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution-NonCommercial International License (CC BY-NC).http://creativecommons.org/licenses/by-nc/4.0/</license-p></license></permissions><abstract><p>
 
 
  Rheumatoid arthritis (RA) is a common form of chronic inflammatory arthritis, and it mainly causes the destruction of small joints. The development of this disease is a relatively secret and repeated process, and therefore early diagnosis and evaluation of the disease is usually difficult. In this study, an arthritis model was successfully induced by injecting complete Freund’s adjuvant (CFA) into the toes of lower limbs of Wistar rats. Seven days after injection of CFA, obvious redness and swelling appeared at the toe joints of lower limbs accompanied by more sensitivity to thermal stimulation. Using the ultraweak bio-photon imaging system (UBIS) established by us, the toe joint area of the lower limbs of rats was imaged 7 days after injection of CFA. It was found that the volar part of lower limbs of arthritis rats showed significantly higher biophoton emissions compared with the control group. The results of this study may provide a basis for further research and devel-opment of early diagnosis and assessment of lesion progression of rheumatoid arthritis.
 
</p></abstract><kwd-group><kwd>Rheumatoid Arthritis</kwd><kwd> Freund’s Adjuvant</kwd><kwd> Biophoton</kwd><kwd> Biophoton Imaging</kwd><kwd> Rat</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. INTRODUCTION</title><p>Rheumatoid arthritis (RA) is the most common chronic inflammatory disease [<xref ref-type="bibr" rid="scirp.112348-ref1">1</xref>], and its main clinical manifestations are symmetry persistent joint swelling and pain. It is also considered a syndrome, including extraarticular manifestations, such as rheumatoid nodules, pulmonary involvement or vasculitis, and systemic complications. With the progress of disease course, patients with RA will have limited joint function due to joint pain and stiffness [2 - 6], however, early diagnosis and evaluation of the disease process are usually difficult, and comprehensive evaluation needs to be combined with multiple detection methods. Therefore, it is of great clinical value to establish a simple technique for early diagnosis and evaluation of disease progress.</p><p>Ultraweak photon emission (UPE), also known as biophoton, exists in almost all organisms with a spectral range of 200 - 800 nm, and an intensity of 10<sup>2</sup> - 10<sup>3</sup> photons/(cm<sup>2</sup>·s) [7 - 10]. Biophoton emissions are directly related to the free radical activity in the process of oxidative metabolism, as well as the physiological and pathological changes of the body, whereas the process of inflammation is often accompanied by the increase of free radical activity. Therefore, the detection of biophoton emission has a certain value in the pathological diagnosis in animals and plants [11 - 16]. In this study, by detecting and analyzing the intensity of biophoton emissions in the toe joint area of lower limbs in rats, we strived to establish a biophoton imaging technology that can be applied to the early diagnosis and disease process evaluation in patients with arthritis.</p></sec><sec id="s2"><title>2. MATERIAL AND METHODS</title><sec id="s2_1"><title>2.1. Rat Model of RA</title><p>Male Wistar rat (3 - 4 weeks, 62 &#177; 5 g) were purchased from Hubei Provincial Laboratory Animal Public Service Center (Wuhan, China) and housed under standard conditions (12-h light/dark cycle, room temperature 18˚C - 25˚C, 40% - 50% humidity) with access to food and water ad libitum. The protocols were approved by the committee on the Ethics of Animal Experiments of South-Central university for Nationalities. Ten rats were divided into two groups (5 in each group and numbered). Complete Freund’s adjuvant (CFA) was injected subcutaneously in the plantar part of the right hind paw of one group and the left hind paw of the other group, and the contralateral hind paw was set as the control. The dose of the first injection was 0.25 ml/100 g and the control was injected with the same dose of normal saline. The changes in diet and activity and the state of lower limb joints of rats in two groups were observed every day.</p></sec><sec id="s2_2"><title>2.2. Pain Sensitivity Test</title><p>Heat sensitivity of the rat hind paw was determined using a Plantar Test Apparatus (ZH-200, Zhenghuabiologic, China). Rat was placed in a plastic box with a glass floor. After a 3-min habituation period, the plantar surface of hind paw was exposed to a beam of radiant heat through the glass floor. The baseline latencies were averaged over 4 trials, separated by a 10-min interval. The test was carried out once a day. A total of 17 tests were conducted, including the first one before CFA injection.</p></sec><sec id="s2_3"><title>2.3. Biophoton Imaging</title><p>The rat’s hind paw was imaged with UBIS according to the previous report [<xref ref-type="bibr" rid="scirp.112348-ref17">17</xref>]. The rat was fixed on a device and then put into the dark box of UBIS. The biophoton imaging was carried out with an EM-CCD. The specific imaging parameters were as follows: 1) EM-CCD cooling temperature is −95˚C; 2) 1200&#215; gain; 3) the exposure time is 900 s for each frame image; 4) the time course of imaging is 1.5 h.</p></sec><sec id="s2_4"><title>2.4. Image Processing and Data Analysis</title><p>A series of images were processed using the previously reported methods [<xref ref-type="bibr" rid="scirp.112348-ref17">17</xref>], including the removal of bright spots caused by the cosmic radiation, and the extraction of gray values from the region of interesting (ROI), such as the plantar joint of the hind limb of rat and background area.</p><p>Relative gray values (RGVs) = the gray values of the region of interesting (ROI) − the gray values of background area.</p></sec><sec id="s2_5"><title>2.5. Statistics</title><p>Statistical analyses were performed using Microsoft Excel and two-tailed paired T-test was used to compare the differences between the treated group and control group. Probability values of p &lt; 0.05 were regarded as significant.</p></sec></sec><sec id="s3"><title>3. RESULTS</title><sec id="s3_1"><title>3.1. CFA-Induced Rat Model of RA</title><p>During the experiment, except that the experimental group had different degrees of claudication in the lower limbs after injection of CFA for a period of time, no obvious behavioral abnormalities and weight changes were found in two groups. Seven days after injection of CFA, the plantar joint of rat hind limb presented swelling (<xref ref-type="fig" rid="fig1">Figure 1</xref>(A)), whereas the hind paws in controls had no such phenomenon (<xref ref-type="fig" rid="fig1">Figure 1</xref>(B)).</p></sec><sec id="s3_2"><title>3.2. Changes in Nociceptive Threshold</title><p>As shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>, there was no difference between the plantar part of the right and left hind paw in two groups before CFA injection. Heat hyperalgesia was found in the CFA injection hind paw lasting from the second day after CFA injection to the 16th days. The most obvious pain sensitive reaction was at the 7th day after injection. A slow recovery process occurred until 12th day, and then there was a period of increased sensitivity.</p><p>The dynamic changes in the reaction time of the hind paw both in RA and control groups.</p></sec><sec id="s3_3"><title>3.3. Biophoton Emissions Were Higher in RA</title><p>A swollen hind paw picture (<xref ref-type="fig" rid="fig3">Figure 3</xref>(A)) in a CFA treated rat corresponds to an image of biophoton imaging (<xref ref-type="fig" rid="fig3">Figure 3</xref>(B)). The regular picture and the image of biophoton imaging in a control rat hind paw are shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>(C) and <xref ref-type="fig" rid="fig3">Figure 3</xref>(D), respectively. There was a significant decline of biophoton emission during the first 30 min, then a slightly decay was observed within the next 60 min. The biophoton emissions were significantly higher in the CFA treated paws than that in the controls at the different time points (<xref ref-type="fig" rid="fig3">Figure 3</xref>(E), <xref ref-type="table" rid="table1">Table 1</xref>, n = 7).</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Comparison of relative gray values between the CFA treated and control hind paws at the different time points</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Time (min)</th><th align="center" valign="middle" >Treated</th><th align="center" valign="middle" >Control</th><th align="center" valign="middle" >P value</th></tr></thead><tr><td align="center" valign="middle" >15</td><td align="center" valign="middle" >104.8 &#177; 37.90</td><td align="center" valign="middle" >84.54 &#177; 23.78</td><td align="center" valign="middle" >0.29</td></tr><tr><td align="center" valign="middle" >30</td><td align="center" valign="middle" >55.71 &#177; 14.39</td><td align="center" valign="middle" >34.62 &#177; 9.86</td><td align="center" valign="middle" >0.012**</td></tr><tr><td align="center" valign="middle" >45</td><td align="center" valign="middle" >42.33 &#177; 7.52</td><td align="center" valign="middle" >26.11 &#177; 6.64</td><td align="center" valign="middle" >0.0019***</td></tr><tr><td align="center" valign="middle" >60</td><td align="center" valign="middle" >36.56 &#177; 3.87</td><td align="center" valign="middle" >20.18 &#177; 4.32</td><td align="center" valign="middle" >0.000016***</td></tr><tr><td align="center" valign="middle" >75</td><td align="center" valign="middle" >29.85 &#177; 4.94</td><td align="center" valign="middle" >17.45 &#177; 5.07</td><td align="center" valign="middle" >0.0011**</td></tr><tr><td align="center" valign="middle" >90</td><td align="center" valign="middle" >29.67 &#177; 5.32</td><td align="center" valign="middle" >15.13 &#177; 6.79</td><td align="center" valign="middle" >0.0014**</td></tr></tbody></table></table-wrap><p>Asterisks indicate a significant difference, n = 7, **p &lt; 0.01; ***p &lt; 0.001.</p></sec></sec><sec id="s4"><title>4. DISCUSSION</title><p>Rheumatoid arthritis is the most commonly diagnosed systemic inflammatory arthritis, and it carries substantial burden for both the individual and society. For individual, they may suffer from some musculoskeletal deficits, cumulative comorbid risk and quality of life [<xref ref-type="bibr" rid="scirp.112348-ref18">18</xref>]. For society, not only it will cost medical resources, but also, as a consequence of functional disability, it may directly relate to the reduced work capacity and decreased societal participation [<xref ref-type="bibr" rid="scirp.112348-ref19">19</xref>]. However, up to now there are no reliable diagnostic criteria for rheumatoid arthritis [<xref ref-type="bibr" rid="scirp.112348-ref20">20</xref>], and it needs to combine many parameters including the clinical symptoms and the various experimental tests and imaging techniques such as radiological imaging and blood and serology assessment, etc. [21 , 22], therefore, the early diagnosis and evaluation of the disease process is usually difficult. In this study, we found that the biophoton emission in the hind paws of RA rats was significantly higher than that of the control group, indicating that this novel biophoton imaging technique may give a new way to solve this problem.</p><p>Many studies have shown that nonspecific inflammation plays an important role in the development of RA, accompanied by increased formation of free radicals [<xref ref-type="bibr" rid="scirp.112348-ref23">23</xref>]. The generation of free radicals is also an important source of biophotons [<xref ref-type="bibr" rid="scirp.112348-ref10">10</xref>]; therefore, by monitoring the degree of joint biophoton emission, it is not only possible to realize the early diagnosis of RA, but also to monitor the development of disease. In addition, this technique also provides a new method for further using RA animal model to study its pathogenesis and develop new drugs.</p></sec><sec id="s5"><title>ACKNOWLEDGEMENTS</title><p>This work was supported by the research funds of South-Central University for Nationalities (XTZ15014 and CZP 18008).</p></sec><sec id="s6"><title>CONFLICTS OF INTEREST</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>REFERENCES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.112348-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Cross, M., Smith, E., Hoy, D., Carmona, L., Wolfe, F., Vos, T., Williams, B., Gabriel, S., Lassere, M., Johns, N., Buchbinder, R., Woolf, A. and March, L. (2014) The Global Burden of Rheumatoid Arthritis: Estimates from the Global Burden of Disease 2010 Study. 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