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 <!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "http://jats.nlm.nih.gov/publishing/1.0/JATS-journalpublishing1.dtd"> <article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="research-article" dtd-version="1.0" xml:lang="en">
  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">IPJ</journal-id>
      <journal-title-group>
        <journal-title>International Physiology Journal</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2578-8590</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">IPJ-19-2623</article-id>
      <article-id pub-id-type="doi">10.14302/issn.2578-8590.ipj-19-2623</article-id>
      <article-categories>
        <subj-group>
          <subject>research-article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Effect of Neosaxitoxin on Epidural Anesthesia in Cats: a Promising Alternative to Conventional Anesthetics</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Xaviera</surname>
            <given-names>Varela</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Miguel</surname>
            <given-names>del Campo</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Robin</surname>
            <given-names>Piron</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Joaquín</surname>
            <given-names>Sepulveda</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Tamara</surname>
            <given-names>Bustamante</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Jaime</surname>
            <given-names>Hinzpeter</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843372660">2</xref>
          <xref ref-type="aff" rid="idm1843274140">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Néstor</surname>
            <given-names>Lagos</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843374820">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843374820">
        <label>1</label>
        <addr-line>Membrane Biochemistry Laboratory, Department of Physiology and Biophysics, Faculty of Medicine – University of Chile. Independencia 1027, Zip Code 8380000, Santiago, Chile.</addr-line>
      </aff>
      <aff id="idm1843372660">
        <label>2</label>
        <addr-line>Department of Orthopaedic Surgery, Clinical Hospital, University of Chile, Santos Dumontt # 999, Independencia, Zip Code: 8380456, Santiago, Chile.</addr-line>
      </aff>
      <aff id="idm1843274140">
        <label>*</label>
        <addr-line>Corresponding author </addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Nasim</surname>
            <given-names>Habibzadeh</given-names>
          </name>
          <xref ref-type="aff" rid="idm1843126428">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1843126428">
        <label>1</label>
        <addr-line>PhD in Sport Science, Department of Sport Science, Teesside University, UK.</addr-line>
      </aff>
      <author-notes>
        <corresp>
    
    Jaime Hinzpeter, <addr-line>Department of Orthopaedic Surgery, Clinical Hospital, University of Chile, Santos Dumontt # 999, Independencia, Independencia 1027, Zip Code 8380000, Santiago, Chile</addr-line>, Email: <email>nlagos@med.uchile.cl</email></corresp>
        <fn fn-type="conflict" id="idm1843139500">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2019-02-07">
        <day>07</day>
        <month>02</month>
        <year>2019</year>
      </pub-date>
      <volume>2</volume>
      <issue>2</issue>
      <fpage>4</fpage>
      <lpage>10</lpage>
      <history>
        <date date-type="received">
          <day>23</day>
          <month>01</month>
          <year>2019</year>
        </date>
        <date date-type="accepted">
          <day>24</day>
          <month>01</month>
          <year>2019</year>
        </date>
        <date date-type="online">
          <day>07</day>
          <month>02</month>
          <year>2019</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2019</copyright-year>
        <copyright-holder>Xaviera Varela</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/ipj/article/993">This article is available from http://openaccesspub.org/ipj/article/993</self-uri>
      <abstract>
        <p>Neosaxitoxin (NeoSTX) is a specific high-affinity inhibitor of voltage-dependent sodium channels, which has shown excellent results as a local anesthetic in various pathologies and post-operative protocols, since it effect is long-lasting and have virtually no side effects.The aim of this study was to analyze the effect of NeoSTX as an                   epidural anesthetic in female cats, undergoing ovariohysterectomy, compared to Lidocaine in a randomized and          double-blind study. Two groups of 11 female cats were randomly in the NeoSTX group and the lidocaine group. They were administered, respectively, a single dose of NeoSTX (0.5 μg / kg) or lidocaine (4 mg / kg, 2%) by epidural via. Using the UNESP-Botucatu pain assessment scale, which considers multiple behavioral and physiological factors, the epidural anesthetic effect of NeoSTX and lidocaine was evaluated, up to 240 min after the                     ovariohysterectomy procedure. NeoSTX no altered the peripheral blood pressure during the cut of uterine cervix, and generated lower values on the pain scale as compared to the lidocaine treatment. None of the cats anesthetized with NeoSTX required an extra dose of pain-relieving drugs (2 mg / kg of tramadol) during the first 150 min after surgery, whereas nine cats from the lidocaine group did need an extra dose of analgesic. NeoSTX is a powerful pain blocker, with a long-lasting anesthetic effect when administered by an epidural procedure. Therefore, NeoSTX emerges as a promising alternative to conventional anesthetics for the treatment of postoperative pain.</p>
      </abstract>
      <kwd-group>
        <kwd>Paralytic Shellfish Toxins</kwd>
        <kwd>Neosaxitoxin</kwd>
        <kwd>Epidural anaesthesia</kwd>
        <kwd>Pain Management</kwd>
      </kwd-group>
      <counts>
        <fig-count count="2"/>
        <table-count count="1"/>
        <page-count count="7"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1843131036" sec-type="intro">
      <title>Introduction</title>
      <p>Epidural anesthesia is a clinical procedure that aims to control pain during surgery and the   postoperative period, in which a local anesthetic is administered into the epidural space, outside the   meninges of the spinal cord, to desensitize the sensory nerve endings that innervate the abdominal wall and the sacral nerve. The most used technique in veterinary medicine of small animals is to administer a local    anesthetic between the vertebrae L7 S1, being lidocaine and bupivacaine the most commonly used drugs. Besides, systemic analgesics such as fentanyl, morphine, tramadol and dissociative anesthetics as ketamine, or combinations of these have been used with different results in terms of their anesthetic effect and duration times <xref ref-type="bibr" rid="ridm1843007980">18</xref>. However, for lidocaine and bupivacaine the duration of their anesthetic effects does not exceed 2 hours, and when they are combined with opioids, although the effect was prolonged, multiple side effects have been described, such as pruritus, central nervous system disorders, seizures and cardiovascular                  depression <xref ref-type="bibr" rid="ridm1843007980">18</xref><xref ref-type="bibr" rid="ridm1843062188">10</xref>. Therefore there is a need to find new epidural anesthetics for veterinary use that have a prolonged effect on pain control without side effects.</p>
      <p>Biotoxins of microalga origin have been used in biomedicine for various purposes, but it is of special interest to highlight the medical use of the toxins that cause paralytic shellfish poisoning (PSP), because of their long-lasting local anesthetic effect <xref ref-type="bibr" rid="ridm1843035788">13</xref>. The PSP toxins correspond to a large group of alkaloids produced by several species of marine dinoflagellates and               freshwater cyanobacteria <xref ref-type="bibr" rid="ridm1843057580">9</xref>. The basic chemical structure of the PSP toxins corresponds to a tricyclic tetrahydropurine, derived from imidazole                     guanidine-type, non-peptidic molecules, which allows several chemical substitutions, giving rise to more than thirty compounds that are analogs of Saxitoxin (STX), which is the base structure and reference of the PSP toxins. Neosaxitoxin (NeoSTX) differs from STX by the addition of a hydroxyl group. These molecules are thermostable and hydrophilic <xref ref-type="bibr" rid="ridm1843049180">14</xref>. PSP toxins are highly specific blockers of voltage-gated sodium channels. These channels are responsible for the propagation of action potentials in neurons, myocytes and other   excitable cells. They are constituted by a subunit α that interacts with the sodium ions on the outer side of the membrane and by one or two subunits that               modulate their activity. In mammals, there are 9 types of subunit α, called NAv 1.1 to NAv 1.9, varying in sequence (approximately 50%) and in the tissues in which they are expressed <xref ref-type="bibr" rid="ridm1843089764">4</xref>. The major Navs in the central nervous system (Nav 1.1, 1.2, 1.3 and 1.6) are inhibited by NeoSTX at nMolar concentrations <xref ref-type="bibr" rid="ridm1843297868">2</xref>.</p>
      <p>The use of PSP toxins, and specifically NeoSTX, in human and veterinary medicine is extensive and well documented, with more than 20 clinical studies for multiple pathologies and post-operative protocols published, where it has been able to establish its                              potent effect as muscle relaxant and local                                    anesthetic <xref ref-type="bibr" rid="ridm1842997812">20</xref><xref ref-type="bibr" rid="ridm1843035788">13</xref><xref ref-type="bibr" rid="ridm1843046660">15</xref><xref ref-type="bibr" rid="ridm1843013740">16</xref><xref ref-type="bibr" rid="ridm1843020220">19</xref>. Its utilization as an anesthetic is highlighted by the generation of                    long-lasting effects compared to conventional        anesthetics, without side effects <xref ref-type="bibr" rid="ridm1843035788">13</xref>. The aim of this work was to evaluate NeoSTX as an epidural anesthetic for the control of postoperative pain after feline                            ovariohysterectomy, in comparison with the anesthetic effect of lidocaine, in a randomized and                            investigator-blind study. For this purpose, the                  multidisciplinary pain assessment scale UNESP-Botucatu was used <xref ref-type="bibr" rid="ridm1843086524">5</xref>. It was decided to opt for the                      UNESP-Botucatu pain scale since it is supported by multiple studies and homologations <xref ref-type="bibr" rid="ridm1843085516">6</xref><xref ref-type="bibr" rid="ridm1843070236">7</xref>, and it has already been used for comparative studies between different anesthetic drugs administered by the epidural route <xref ref-type="bibr" rid="ridm1843042628">11</xref>. This evaluation considers multiple behavioral and physiological factors and is divided into three areas of measurement: Psychomotor disorders (posture, comfort, activity, attitude and various behaviors); Protection of the painful area and vocal expression of the pain (reaction to the palpation of the surgical wound, reaction to the palpation of the abdomen and vocalization); and Physiological variables (peripheral blood pressure and appetite). In addition, the need to apply rescue medication (tramadol) to the patients was evaluated in both groups, according to the values obtained in the pain scale.</p>
    </sec>
    <sec id="idm1843131108" sec-type="materials">
      <title>Materials and Methods</title>
      <p>The evaluation of the epidural anesthetic effect of NeoSTX and lidocaine in the postoperative period after an ovariohysterectomy, was performed as follows: 22 feline females, of domestic or common European breed, from 6 months to 2 years of age, were voluntarily taken by their owners to the Diego Silva Veterinary Clinic, (Conchalí, Santiago de Chile), where the              procedure was explained informed consent was given. The procedure was free of charge for the owner. The Bioethical Committee of the Diego Silva Veterinary Clinic; and the Bioethical Committee on Animal                Experimentation the Faculty of Medicine, University of Chile (FM 0551), approved the experimental procedures.</p>
      <p>The cats were randomly divided into two groups, NeoSTX and lidocaine, using the SPSS software. Both the veterinarian in charge of the ovariohysterectomy and the veterinarian who performed the pain assessment worked blindly, without knowing which anesthetic was being used.</p>
      <p>In both groups, the endotracheal intubation was introduced, which was connected to an anesthesia machine, supplying Isoflurane at an initial concentration of 3% using a vaporizer, which was varied according to the patients' requirement (1.5 - 3%). Oxygen was provided at a rate of 20 mL kg<sup>-1</sup> minute<sup>-1</sup>. Then, the cephalic vein was cannulated with a venous catheter, through which 0.9 % sodium chloride solution at a dose of 10 mL kg<sup>-1 </sup>hour<sup>-1</sup>, was administered as a maintenance fluid. No cat was previously treated with any drug. Anesthesia was induced with a bolus of Propofol at 3 mg / kg intravenously. Once the appropriate anesthetic level was reached, NeoSTX (0.5 μg/kg) or lidocaine               (4 mg / kg, 2 %, Virbac®) were placed in epidural via. NeoSTX was purified according to Riquelme et al., 2018.</p>
      <p>Then Peripheral blood pressure was                       measurement with a pediatric cuff and vascular Doppler sphygmomanometer (Sonoline B Doppler 8 mhz)                  pre-surgical, and an average of 3 continuous                 measurement was taken. Then, in the pavilion, the peripheral blood pressure was measured throughout the surgical procedure and recorded at the beginning of surgery, post cervix cut and at the end of the surgical procedure.</p>
      <p>Afterwards the patients were transferred to the recovery room and 30 min after the endotracheal extubation, the evaluation of postoperative analgesia was started, which was carried out every 30 min until completing a period of 240 min, based on the                  multidimensional scale of the UNESP-Botucatu <xref ref-type="bibr" rid="ridm1843070236">7</xref>. It should be noted that previous to the start of the surgical procedure, patients were evaluated to establish the baseline value on the pain scale.</p>
      <p>The variables were evaluated with response options numbered from 0 to 3, indicating the degree of pain. Thus 0 indicated absence of pain, 1 mild pain, 2 moderate pain and 3 severe pain. The sum of scores of all the variables can give a total of 30 points which defined the degree of pain of the patient: between 1 and 9 points indicated mild pain, between 10 and 19 points indicated moderate pain and between 20 and 30 points severe pain. Patients who scored higher than 10 for more than two consecutive evaluations were given the emergency analgesic tramadol at a dose of 2 mg / kg intramuscularly <xref ref-type="bibr" rid="ridm1843070236">7</xref>.</p>
      <p>The data collected were grouped into                 criteria based on the multidimensional scale of                                UNESP - Botucatu, generating averages for each group with a standard deviation equivalent to P ≤ 0.5 using student's T.</p>
    </sec>
    <sec id="idm1843128876" sec-type="results">
      <title>Results </title>
      <p>When the peripheral blood pressure of the patients of the NeoSTX group was compared, no  difference could be observed between the pressure before the surgery and at the moment of the cervix cut. This is indicative of a total state of anesthesia achieved by NeoSTX, which demonstrates its effectiveness and anesthetic power. However, in the group anesthetized with lidocaine, an increase in pressure was observed when the cervix was cut, as compared to its basal state, and also as compared to the peripheral blood pressure of the NeoSTX group (<xref ref-type="fig" rid="idm1842751924">Figure 1</xref>). At the end of the procedure, the peripheral blood pressure in both groups had returned to their basal levels.</p>
      <fig id="idm1842751924">
        <label>Figure 1.</label>
        <caption>
          <title> Effect of NeoSTX and lidocaine on peripheral blood pressure, comparison of the pressure before surgery (basal) and the pressure at the moment when the cervix was cut. The NeoSTX group does not show differences, while for the lidocaine group an increase in peripheral blood pressure is observed when both measurements are compared. Significance determined with T test: * p &lt;0.05, ** p &lt;0.01.</title>
        </caption>
        <graphic xlink:href="images/image1.jpeg" mime-subtype="jpeg"/>
      </fig>
      <p>The pain assessment scale of UNESP-Botucatu was measured for all patients prior to the surgery to establish the reference level and every 30 min after the procedure, for a total duration of up to 240 min. The higher the score is on this evaluation, the greater the discomfort of the patient is. The final results are shown in <xref ref-type="fig" rid="idm1842725636">Figure 2</xref>A. Both groups have the same preoperative score (around 2 points, score described in <xref ref-type="bibr" rid="ridm1843070236">7</xref>, for control animals), but then, 30 min after the surgery, the score of the lidocaine group shows a sudden and       significant increase for up to 150 min, as compared to the NeoSTX group, while the score of the NeoSTX group remains low. These low values reflect a deep anesthetic state that is also observed in the values of the                 subgroups 1 and 2 of the measurement of the                UNESP-Botucatu method, these are: Psychomotor disorders (<xref ref-type="fig" rid="idm1842725636">Figure 2</xref>B) and Protection of the painful area and the vocal expression of pain (<xref ref-type="fig" rid="idm1842725636">Figure 2</xref>C). For subgroup 3 (<xref ref-type="fig" rid="idm1842725636">Figure 2</xref>D), which analyzes the               physiological variables, again lower scores were observed for the NeoSTX group as compared to the lidocaine group, albeit not significant.</p>
      <fig id="idm1842725636">
        <label>Figure 2.</label>
        <caption>
          <title> Pain assessment using the UNESP-Botucatu multidimensional scale: A. Total score; B. Subscale 1, Psychomotor disorders; C. Protection of the painful area and the vocal expression of pain and D. Physiological variables. Significance determined with T test: *** p &lt;0.001.</title>
        </caption>
        <graphic xlink:href="images/image2.jpg" mime-subtype="jpg"/>
      </fig>
      <p>Already at 30 min after surgery the average pain score of the lidocaine group exceeded 10 (<xref ref-type="fig" rid="idm1842751924">Figure 1</xref>A). As a result, 9 out of 11 patients in the lidocaine group had to be given a rescue dose of tramadol at 60 min, the requisite for which were 2 consecutive pain scores of 10 or more for a given patient, while the remaining 2 patients eventually received a dose at 180 min (<xref ref-type="table" rid="idm1842721460">Table 1</xref>). In contrast to the lidocaine group, the average pain score of the NeoSTX group only exceeded 10 after 210 min. Consequently, the first patient had to be rescued at 150 min, and a second one at 180 min, the point in time at which all 11 patients of the lidocaine group had been rescued. Moreover 3 more patients received a dose at 210 min, while the remaining 6 patients (more than half of the cohort) were rescued only after 240 min at the end of the experiment. </p>
      <table-wrap id="idm1842721460">
        <label>Table 1.</label>
        <caption>
          <title> Number of patients and time at which tramadol was applied as emergency medication to  reduce excessive pain, comparison of lidocaine and NeoSTX treatments for epidural anesthesia</title>
        </caption>
        <table rules="all" frame="box">
          <tbody>
            <tr>
              <td> </td>
              <td> </td>
              <td> </td>
              <td> </td>
              <td> </td>
              <td>Time(min)</td>
              <td> </td>
              <td> </td>
              <td> </td>
              <td> </td>
            </tr>
            <tr>
              <td> </td>
              <td>30</td>
              <td>60</td>
              <td>90</td>
              <td>120</td>
              <td>150</td>
              <td>180</td>
              <td>210</td>
              <td>240</td>
              <td>Total</td>
            </tr>
            <tr>
              <td>Lidocaine</td>
              <td>0</td>
              <td>9</td>
              <td>0</td>
              <td>0</td>
              <td>0</td>
              <td>2</td>
              <td>0</td>
              <td>0</td>
              <td>11</td>
            </tr>
            <tr>
              <td>Neosaxitoxin</td>
              <td>0</td>
              <td>0</td>
              <td>0</td>
              <td>0</td>
              <td>1</td>
              <td>1</td>
              <td>3</td>
              <td>6</td>
              <td>11</td>
            </tr>
          </tbody>
        </table>
      </table-wrap>
      <p>Since there were 9 patients in the lidocaine group who received tramadol after 60 min, the values on the pain scale had a tendency to decrease (<xref ref-type="fig" rid="idm1842751924">Figure 1</xref>A). The effect of tramadol on the NeoSTX group is not reflected in the overall pain scores that show a tendency to increase towards the end of the experiment, because the majority of the patients in this group received the drug only after 210 or 240 min close to the end of the experiment. It should be noted that even though most of the patients of the lidocaine group were treated with the rescue drug early on (60 min), the group did not show lower values on the pain scale than the NeoSTX group for up to 210 min after surgery.</p>
      <p>In summary, the animals that received NeoSTX as epidural anesthesia did not show an increase in their peripheral blood pressure during the surgical procedure or in the post-surgery period in relation to their baseline values. Moreover, they scored significantly lower on the UNESP-Botucatu pain assessment scale as compared to the lidocaine group. Furthermore after 180 min, when the entire lidocaine group had received a rescue dose, only 2 NeoSTX patients needed rescue and half of the NeoSTX cohort was rescued only at the end of the experiment after 240 min. No side effects were observed in any patient anesthetized with NeoSTX.</p>
    </sec>
    <sec id="idm1843065100" sec-type="discussion">
      <title>Discussion </title>
      <p>Lidocaine is the most commonly used local anesthetic for epidural administration in cats and dogs during surgical procedures. However, lidocaine alone is not a good analgesic for controlling surgical and postoperative pain in ovariohysterectomy, because it is highly toxic in felines, when compared to canines, as well as generating significant cardiopulmonary depression when administered together with               Isoflurane <xref ref-type="bibr" rid="ridm1843008628">17</xref>. Although it is a lowrisk, lowcost drug that provides rapidonset anesthesia, its short duration increases postoperative pain scores and increases the requirement for analgesics such as opioids, which generate a series of side effects. In addition, opioids are not effective in the inhibition of A-δ fibers that are responsible for acute pain and are activated by persistent stimuli inflicted by surgical procedures <xref ref-type="bibr" rid="ridm1843007980">18</xref>.</p>
      <p>It has been demonstrated that NeoSTX has a prolonged post-surgery anesthetic effect and is effective at pain control in both human and veterinary                medicine <xref ref-type="bibr" rid="ridm1843035788">13</xref><xref ref-type="bibr" rid="ridm1843046660">15</xref><xref ref-type="bibr" rid="ridm1843020220">19</xref>. Lately, it has become a powerful alternative to the use of conventional anesthetics <xref ref-type="bibr" rid="ridm1843056716">8</xref>. Specifically in cats, the toxicokinetic and toxicodynamic parameters of GTX2/3, analogous to NeoSTX, have been established, showing the clearance of these toxins at 4.6 mL / min kg, mainly by glomerular filtration <xref ref-type="bibr" rid="ridm1843307732">3</xref>.  Taking into account that for the related compound Saxitoxin the LD50 in rats is 7 μg / kg, the dose used in this pilot study was 0.5 μg / kg, which was sufficient to showed favorable results compared to lidocaine (4 mg / kg). Although no side effects were seen in patients that received the NeoSXT dose, we believe that it would be of interests in future studies to determine the lower threshold dose of needed to obtain the same effect.</p>
      <p>In this study, the epidural anesthetic effect of NeoSTX was compared to lidocaine in an                       ovariohysterectomy surgical intervention, using the UNESP-Botucatu pain assessment scale, which is widely used in veterinary medicine. This measurement of postsurgery pain includes both the interpretative measurements of the veterinarian in charge and analytical data, particularly the peripheral blood pressure. The visceral pain produced in surgical procedures causes an increase in the sympathetic tone that generates vasoconstriction and an increase in cardiac output, which leads to an increase in peripheral blood pressure <xref ref-type="bibr" rid="ridm1843233108">1</xref> The latter is the most reliable physiological parameter as an indicator to measure pain in cats <xref ref-type="bibr" rid="ridm1843039892">12</xref>. As seen in <xref ref-type="fig" rid="idm1842751924">Figure 1</xref>, patients anesthetized with NeoSTX maintained a peripheral blood pressure level equal to that observed during and after              ovariohysterectomy, unlike patients anesthetized with lidocaine, where peripheral blood pressure increased during the surgical procedure, which is indicative of pain.</p>
      <p>The results of the postoperative analgesic evaluation with the multidisciplinary scale of UNESPBotucatu <xref ref-type="bibr" rid="ridm1843070236">7</xref> show that the NeoSTX group not exceed 10 points on average on the total pain scale, for up to 180 min, which is indicative of a good level of analgesia, and is the result of a better performance of the NeoSTX patients in the three groups of parameters measured (Psychomotor disorders, Protection of the painful area and vocal expression of pain, and Physiological variables) in comparison to lidocaine (<xref ref-type="fig" rid="idm1842725636">Figure 2</xref>). In addition, this score was significantly lower than that obtained by the lidocaine group, which had an average score higher than 13 (moderate pain) after 60 min, which forced veterinarians to administer emergency medications to 9 of the 11 patients. </p>
      <p>Even after administration of the rescue dose, the lidocaine group’s pain scores remained significantly higher than those of the NeoSTX group for the first 210 min, clearly showing that the NeoSTX treatment was more effective at pain control postsurgery.</p>
      <p>It is demonstrated in this work that NeoSTX, through the epidural way, is a powerful post-surgery pain blocker in ovariohysterectomy in cats, being more effective and long lasting than lidocaine, without having side effects. </p>
    </sec>
  </body>
  <back>
    <ref-list>
      <ref id="ridm1843233108">
        <label>1.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Hellyer</surname>
            <given-names>P</given-names>
          </name>
          <name>
            <surname>Rodan</surname>
            <given-names>I</given-names>
          </name>
          <name>
            <surname>2-Brunt</surname>
            <given-names>J</given-names>
          </name>
          <name>
            <surname>Downing</surname>
            <given-names>R</given-names>
          </name>
          <name>
            <surname>J</surname>
            <given-names>E Hagedorn</given-names>
          </name>
          <article-title>(2007).American Animal Hospital Association, American Association of Feline Practitioners,AAHA/AAFP Pain Management Guidelines Task Force Members, AAHA/AAFP pain management guidelines for dogs &amp; cats.J. Am Anim</article-title>
          <source>Hosp Assoc</source>
          <volume>43</volume>
          <fpage>235</fpage>
          <lpage>248</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843297868">
        <label>2.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Alonso</surname>
            <given-names>E</given-names>
          </name>
          <name>
            <surname>Alfonso</surname>
            <given-names>A</given-names>
          </name>
          <name>
            <surname>M</surname>
            <given-names>R Vieytes</given-names>
          </name>
          <name>
            <surname>L</surname>
            <given-names>M Botana</given-names>
          </name>
          <article-title>Evaluation of toxicity equivalent factors of paralytic shellfish poisoning toxins in seven humansodium channels types by an automated high throughput electrophysiology system</article-title>
          <date>
            <year>2016</year>
          </date>
          <source>Arch. Toxicol</source>
          <volume>90</volume>
          <fpage>479</fpage>
          <lpage>488</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843307732">
        <label>3.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Andrinolo</surname>
            <given-names>D</given-names>
          </name>
          <name>
            <surname>Iglesias</surname>
            <given-names>V</given-names>
          </name>
          <name>
            <surname>García</surname>
            <given-names>C</given-names>
          </name>
          <name>
            <surname>Lagos</surname>
            <given-names>N</given-names>
          </name>
          <article-title>Toxicokinetics and toxicodynamics of gonyautoxins after an oral toxin dose in cats</article-title>
          <date>
            <year>2002</year>
          </date>
          <source>Toxicon</source>
          <volume>40</volume>
          <fpage>699</fpage>
          <lpage>709</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843089764">
        <label>4.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>W</surname>
            <given-names>A Catterall</given-names>
          </name>
          <article-title>From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels</article-title>
          <date>
            <year>2000</year>
          </date>
          <source>Neuron</source>
          <volume>26</volume>
          <fpage>13</fpage>
          <lpage>25</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843086524">
        <label>5.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Brondani</surname>
            <given-names>J</given-names>
          </name>
          <name>
            <surname>Luna</surname>
            <given-names>S</given-names>
          </name>
          <name>
            <surname>Padovani</surname>
            <given-names>C</given-names>
          </name>
          <article-title>Refinement and initial validation of a multidimensional composite scale for use in assessing acute postoperative pain in cats</article-title>
          <date>
            <year>2011</year>
          </date>
          <source>Am. J. Vet. Res</source>
          <volume>72</volume>
          <fpage>174</fpage>
          <lpage>183</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843085516">
        <label>6.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>J</surname>
            <given-names>T Brondani</given-names>
          </name>
          <name>
            <surname>K</surname>
            <given-names>R Mama</given-names>
          </name>
          <name>
            <surname>S</surname>
            <given-names>P Luna</given-names>
          </name>
          <name>
            <surname>B</surname>
            <given-names>D Wright</given-names>
          </name>
          <name>
            <surname>Niyom</surname>
            <given-names>S</given-names>
          </name>
          <article-title>Validation of the English version of the UNESP-Botucatu multidimensional composite pain scale for assessing postoperative pain in cats</article-title>
          <date>
            <year>2013</year>
          </date>
          <source>BMC. Vet. Res</source>
          <volume>9</volume>
          <fpage>143</fpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843070236">
        <label>7.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>J</surname>
            <given-names>T Brondani</given-names>
          </name>
          <name>
            <surname>Luna</surname>
            <given-names>S P L</given-names>
          </name>
          <name>
            <surname>Crosignani</surname>
            <given-names>N</given-names>
          </name>
          <name>
            <surname>J</surname>
            <given-names>I Redondo</given-names>
          </name>
          <name>
            <surname>Granados</surname>
            <given-names>M M ET al</given-names>
          </name>
          <article-title>Validez y confiabilidad de la versión en español de la escala multidimensional de la UNESP-Botucatu para evaluar el dolor postoperatorio en gatos”</article-title>
          <date>
            <year>2014</year>
          </date>
          <source>Arch. Med. Vet</source>
          <volume>46</volume>
          <fpage>477</fpage>
          <lpage>486</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843056716">
        <label>8.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>J</surname>
            <given-names>F Butterworth</given-names>
          </name>
          <article-title>Will conventional local anesthetics soon be replaced by neurotoxins?</article-title>
          <date>
            <year>2011</year>
          </date>
          <source>Reg. Anesth. Pain Med</source>
          <volume>36</volume>
          <fpage>101</fpage>
          <lpage>102</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843057580">
        <label>9.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>K</surname>
            <given-names>D Cusick</given-names>
          </name>
          <name>
            <surname>G</surname>
            <given-names>S Sayler</given-names>
          </name>
          <article-title>An overview on the marine neurotoxin, saxitoxin: genetics, molecular targets, methods of detection and ecological functions.Mar</article-title>
          <date>
            <year>2013</year>
          </date>
          <source>Drugs</source>
          <volume>27</volume>
          <fpage>991</fpage>
          <lpage>1018</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843062188">
        <label>10.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>DeRossi</surname>
            <given-names>R</given-names>
          </name>
          <name>
            <surname>L</surname>
            <given-names>C Hermeto</given-names>
          </name>
          <name>
            <surname>Jardim</surname>
            <given-names>P H A</given-names>
          </name>
          <name>
            <surname>de</surname>
            <given-names>Andra</given-names>
          </name>
          <name>
            <surname>N</surname>
            <given-names>de Assis</given-names>
          </name>
          <name>
            <surname>T</surname>
            <given-names>K</given-names>
          </name>
          <article-title>Postoperative pain control in cats: clinical trials with pre-emptive lidocaine epidural co-administered with morphine or methadone</article-title>
          <date>
            <year>2016</year>
          </date>
          <source>J. Feline Med. Surg</source>
          <volume>18</volume>
          <fpage>882</fpage>
          <lpage>888</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843042628">
        <label>11.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Fernandez-Parra</surname>
            <given-names>R</given-names>
          </name>
          <name>
            <surname>Zilberstein</surname>
            <given-names>L</given-names>
          </name>
          <name>
            <surname>Fontaine</surname>
            <given-names>C</given-names>
          </name>
          <name>
            <surname>Adami</surname>
            <given-names>C</given-names>
          </name>
          <article-title>Comparison of intratesticular lidocaine, sacrococcygeal epidural lidocaine and intravenous methadone in cats undergoing castration: a prospective, randomized, investigator-blind clinical trial</article-title>
          <date>
            <year>2017</year>
          </date>
          <source>Vet. Anaesth. Analg</source>
          <volume>44</volume>
          <fpage>356</fpage>
          <lpage>363</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843039892">
        <label>12.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>K</surname>
            <given-names>M Tobias</given-names>
          </name>
          <name>
            <surname>R</surname>
            <given-names>C Harvey</given-names>
          </name>
          <name>
            <surname>J</surname>
            <given-names>M Byarlay</given-names>
          </name>
          <article-title>Comparison of four methods of analgesia in cats following ovariohysterectomy</article-title>
          <date>
            <year>2006</year>
          </date>
          <source>Vet. Anaesth. Analg</source>
          <volume>33</volume>
          <fpage>390</fpage>
          <lpage>398</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843035788">
        <label>13.</label>
        <mixed-citation xlink:type="simple" publication-type="book">
          <name>
            <surname>Lagos</surname>
            <given-names>N</given-names>
          </name>
          <article-title>Clinical applications of paralytic shellfish poisoning toxins, in:</article-title>
          <date>
            <year>2014</year>
          </date>
          <chapter-title>Rossini, G.P.(Ed),Toxins and Biologically Active Compounds from Microalgae, Volume 2: Biological Effects and Risk Management.CRCPress.Florida.pp</chapter-title>
          <fpage>309</fpage>
          <lpage>329</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843049180">
        <label>14.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>L</surname>
            <given-names>E</given-names>
          </name>
          <article-title>Saxitoxin, a toxic marine natural product that targets a multitude of receptors</article-title>
          <date>
            <year>2006</year>
          </date>
          <source>Nat. Prod. Rep</source>
          <volume>23</volume>
          <fpage>200</fpage>
          <lpage>222</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843046660">
        <label>15.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Lobo</surname>
            <given-names>K</given-names>
          </name>
          <name>
            <surname>Donado</surname>
            <given-names>C</given-names>
          </name>
          <name>
            <surname>Cornelissen</surname>
            <given-names>L</given-names>
          </name>
          <name>
            <surname>Kim</surname>
            <given-names>J</given-names>
          </name>
          <name>
            <surname>Ortiz</surname>
            <given-names>R</given-names>
          </name>
          <article-title>A Phase 1, Dose-escalation, Double-blind, Block-randomized, Controlled Trial of Safety and Efficacy of Neosaxitoxin Alone and in Combination with 0.2% Bupivacaine, with and without Epinephrine, for Cutaneous Anesthesia</article-title>
          <date>
            <year>2015</year>
          </date>
          <source>Anesthesiology</source>
          <volume>123</volume>
          <fpage>873</fpage>
          <lpage>885</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843013740">
        <label>16.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Manríquez</surname>
            <given-names>V</given-names>
          </name>
          <name>
            <surname>Caperan</surname>
            <given-names>Castro</given-names>
          </name>
          <name>
            <surname>Guzmán</surname>
            <given-names>D</given-names>
          </name>
          <name>
            <surname>Naser</surname>
            <given-names>R</given-names>
          </name>
          <name>
            <surname>Iglesia</surname>
            <given-names>M</given-names>
          </name>
          <name>
            <surname>V</surname>
            <given-names/>
          </name>
          <article-title>First evidence of neosaxitoxin as a long-acting pain blocker in bladder pain syndrome</article-title>
          <date>
            <year>2015</year>
          </date>
          <source>Int. Urogynecol. J</source>
          <volume>26</volume>
          <fpage>853</fpage>
          <lpage>858</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843008628">
        <label>17.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Pypendop</surname>
            <given-names>B</given-names>
          </name>
          <name>
            <surname>Ilkiw</surname>
            <given-names>J</given-names>
          </name>
          <article-title>Assessment of the hemodynamic effects of lidocaine administered IV in isoflurane-anesthetized cats</article-title>
          <date>
            <year>2005</year>
          </date>
          <source>Am. J. Vet. Res</source>
          <volume>4</volume>
          <fpage>661</fpage>
          <lpage>668</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843007980">
        <label>18.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Valverde</surname>
            <given-names>A</given-names>
          </name>
          <article-title>Epidural analgesia and anesthesia in dogs and cats.Vet</article-title>
          <date>
            <year>2008</year>
          </date>
          <source>Clin. North Am. Small Anim. Pract</source>
          <volume>38</volume>
          <fpage>1205</fpage>
          <lpage>1230</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1843020220">
        <label>19.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>Riquelme</surname>
            <given-names>G</given-names>
          </name>
          <name>
            <surname>J</surname>
            <given-names>M Sepúlveda</given-names>
          </name>
          <name>
            <surname>Ghumgham</surname>
            <given-names>Al</given-names>
          </name>
          <name>
            <surname>Del</surname>
            <given-names>Campo Z</given-names>
          </name>
          <name>
            <surname>Montero</surname>
            <given-names>M</given-names>
          </name>
          <name>
            <surname>C</surname>
            <given-names/>
          </name>
          <article-title>Neosaxitoxin, a Paralytic Shellfish Poison toxin, effectively manages bucked shins pain, as a local long-acting pain blocker in an equine model</article-title>
          <date>
            <year>2018</year>
          </date>
          <source>Toxicon</source>
          <volume>141</volume>
          <fpage>15</fpage>
          <lpage>17</lpage>
        </mixed-citation>
      </ref>
      <ref id="ridm1842997812">
        <label>20.</label>
        <mixed-citation xlink:type="simple" publication-type="journal">
          <name>
            <surname>A</surname>
            <given-names>J Rodriguez-Navarro</given-names>
          </name>
          <name>
            <surname>Lagos</surname>
            <given-names>N</given-names>
          </name>
          <name>
            <surname>Lagos</surname>
            <given-names>M</given-names>
          </name>
          <name>
            <surname>Braghetto</surname>
            <given-names>I</given-names>
          </name>
          <name>
            <surname>Csendes</surname>
            <given-names>A</given-names>
          </name>
          <article-title>Neosaxitoxin as a local anesthetic: preliminary observations from a first human trial</article-title>
          <date>
            <year>2007</year>
          </date>
          <source>Anesthesiology</source>
          <volume>106</volume>
          <fpage>339</fpage>
          <lpage>345</lpage>
        </mixed-citation>
      </ref>
    </ref-list>
  </back>
</article>
