Comparative evaluation of different therapeutic protocols for contagious caprine pleuropneumonia in Himalayan Pashmina goats

Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same l...

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Veröffentlicht in:Tropical animal health and production 2019-11, Vol.51 (8), p.2127-2137
Hauptverfasser: Yatoo, Mohd. Iqbal, Parray, Oveas Raffiq, Mir, Muheet, Bhat, Riyaz Ahmed, Malik, Hamid Ullah, Fazili, Mujeeb ur Rehman, Qureshi, Sabia, Mir, Masood Salim, Yousuf, Raja Wasim, Tufani, Noor Alam, Dhama, Kuldeep, Bashir, Shah Tauseef
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container_title Tropical animal health and production
container_volume 51
creator Yatoo, Mohd. Iqbal
Parray, Oveas Raffiq
Mir, Muheet
Bhat, Riyaz Ahmed
Malik, Hamid Ullah
Fazili, Mujeeb ur Rehman
Qureshi, Sabia
Mir, Masood Salim
Yousuf, Raja Wasim
Tufani, Noor Alam
Dhama, Kuldeep
Bashir, Shah Tauseef
description Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same leads to the development of antibiotic resistance and decreased efficacy of drug. Besides, inflammatory and allergic pathogenesis of CCPP envisages combination therapy. In this study, we evaluated the effectiveness of the combination therapy using different antibiotics (oxytetracycyline @ 10: group I, enrofloxacin @ 5 group II, and tylosin: group III, @ 10 mg/kg body weight), along with anti-inflammatory (meloxicam @ 0.5 mg/kg) and anti-allergic (pheneramine maleate @ 1.0 mg/kg) drugs. These drugs were given intramuscularly at the interval of 48 h for four times in three test groups ( n  = 10) of Pashmina goats, viz. groups I, II, and III, respectively, affected with CCPP. Group IV ( n  = 10) was kept as healthy control when group V ( n  = 10) treated with oxytetracycline @ 10 mg/kg alone was used as positive control. Clinical signs, clinical parameters, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-α)), and oxidative stress indices (total oxidant status (TOS), total antioxidant status (TAS)) were evaluated at hours 0, 48, 96, and 144 of experimental trial. Tylosin-based combination therapy resulted in a rapid and favorable recovery resulting in restoration of normal body temperature (102.46 ± 0.31 °F), respiration rate (16.30 ± 0.79 per minute), and heart rate (89.50 ± 2.63 per minute) compared to the oxytetracycline (102.95 ± 0.13, 21.30 ± 1.12, 86.00 ± 2.33, respectively) and enrofloxacin (102.97 ± 0.19, 21.00 ± 1.25, 90.00 ± 2.58, respectively) treated groups. By hour 144, all the groups showed restoration of clinical parameters of normal health and diminishing signs of CCPP, viz. fever, dyspnea, coughing, nasal discharge, weakness, and pleurodynia. Significant ( P  ≤ 0.05) decrease in levels of TNF-α and non-significant ( P  > 0.05) decrease in levels of TOS and an increase in levels of TAS were noted from hour 0 to 144 in all the test groups. Within the groups, no significant ( P  > 0.05) change was noted in TNF-α, TOS, and TAS levels; however, TNF-α levels were comparatively lower in group III. Hematological parameters did not differ significantly ( P  > 0.05). From these findings, it can be inferred that tylosin-based combination therapy is
doi_str_mv 10.1007/s11250-019-01913-2
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Iqbal ; Parray, Oveas Raffiq ; Mir, Muheet ; Bhat, Riyaz Ahmed ; Malik, Hamid Ullah ; Fazili, Mujeeb ur Rehman ; Qureshi, Sabia ; Mir, Masood Salim ; Yousuf, Raja Wasim ; Tufani, Noor Alam ; Dhama, Kuldeep ; Bashir, Shah Tauseef</creator><creatorcontrib>Yatoo, Mohd. Iqbal ; Parray, Oveas Raffiq ; Mir, Muheet ; Bhat, Riyaz Ahmed ; Malik, Hamid Ullah ; Fazili, Mujeeb ur Rehman ; Qureshi, Sabia ; Mir, Masood Salim ; Yousuf, Raja Wasim ; Tufani, Noor Alam ; Dhama, Kuldeep ; Bashir, Shah Tauseef</creatorcontrib><description>Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same leads to the development of antibiotic resistance and decreased efficacy of drug. Besides, inflammatory and allergic pathogenesis of CCPP envisages combination therapy. In this study, we evaluated the effectiveness of the combination therapy using different antibiotics (oxytetracycyline @ 10: group I, enrofloxacin @ 5 group II, and tylosin: group III, @ 10 mg/kg body weight), along with anti-inflammatory (meloxicam @ 0.5 mg/kg) and anti-allergic (pheneramine maleate @ 1.0 mg/kg) drugs. These drugs were given intramuscularly at the interval of 48 h for four times in three test groups ( n  = 10) of Pashmina goats, viz. groups I, II, and III, respectively, affected with CCPP. Group IV ( n  = 10) was kept as healthy control when group V ( n  = 10) treated with oxytetracycline @ 10 mg/kg alone was used as positive control. Clinical signs, clinical parameters, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-α)), and oxidative stress indices (total oxidant status (TOS), total antioxidant status (TAS)) were evaluated at hours 0, 48, 96, and 144 of experimental trial. Tylosin-based combination therapy resulted in a rapid and favorable recovery resulting in restoration of normal body temperature (102.46 ± 0.31 °F), respiration rate (16.30 ± 0.79 per minute), and heart rate (89.50 ± 2.63 per minute) compared to the oxytetracycline (102.95 ± 0.13, 21.30 ± 1.12, 86.00 ± 2.33, respectively) and enrofloxacin (102.97 ± 0.19, 21.00 ± 1.25, 90.00 ± 2.58, respectively) treated groups. By hour 144, all the groups showed restoration of clinical parameters of normal health and diminishing signs of CCPP, viz. fever, dyspnea, coughing, nasal discharge, weakness, and pleurodynia. Significant ( P  ≤ 0.05) decrease in levels of TNF-α and non-significant ( P  &gt; 0.05) decrease in levels of TOS and an increase in levels of TAS were noted from hour 0 to 144 in all the test groups. Within the groups, no significant ( P  &gt; 0.05) change was noted in TNF-α, TOS, and TAS levels; however, TNF-α levels were comparatively lower in group III. Hematological parameters did not differ significantly ( P  &gt; 0.05). From these findings, it can be inferred that tylosin-based combination therapy is relatively better for early, rapid, and safe recovery besides minimizing inflammatory and oxidative cascade in CCPP affected Pashmina goats compared to oxytetracycline- and enrofloxacin-based therapies.</description><identifier>ISSN: 0049-4747</identifier><identifier>EISSN: 1573-7438</identifier><identifier>DOI: 10.1007/s11250-019-01913-2</identifier><identifier>PMID: 31076996</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animals ; Anti-Allergic Agents - therapeutic use ; Anti-Bacterial Agents - therapeutic use ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Antibiotic resistance ; Antibiotics ; Antioxidants ; Biomedical and Life Sciences ; Body temperature ; Body weight ; Caprinae ; Contagious caprine pleuropneumonia ; Drug Therapy, Combination - veterinary ; Dyspnea ; Enrofloxacin ; Enrofloxacin - therapeutic use ; Female ; Fever ; Goat Diseases - drug therapy ; Goats ; Heart rate ; India ; Inflammation ; Life Sciences ; Meloxicam ; Meloxicam - therapeutic use ; Myalgia ; Oxidative stress ; Oxidizing agents ; Oxytetracycline ; Oxytetracycline - therapeutic use ; Parameters ; Pathogenesis ; Pheniramine - therapeutic use ; Pleuropneumonia ; Pleuropneumonia - veterinary ; Pleuropneumonia, Contagious - drug therapy ; Pneumonia, Mycoplasma ; Recovery ; Regular Articles ; Respiration ; Restoration ; Therapy ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α ; Tylosin ; Tylosin - therapeutic use ; Veterinary Medicine/Veterinary Science ; Zoology</subject><ispartof>Tropical animal health and production, 2019-11, Vol.51 (8), p.2127-2137</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Tropical Animal Health and Production is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-d49e4c40b1cc8a8428f2c7dc53b7055cb4b03dbfe80cb08c1ec508dd7fc13c873</citedby><cites>FETCH-LOGICAL-c375t-d49e4c40b1cc8a8428f2c7dc53b7055cb4b03dbfe80cb08c1ec508dd7fc13c873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11250-019-01913-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11250-019-01913-2$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31076996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yatoo, Mohd. Iqbal</creatorcontrib><creatorcontrib>Parray, Oveas Raffiq</creatorcontrib><creatorcontrib>Mir, Muheet</creatorcontrib><creatorcontrib>Bhat, Riyaz Ahmed</creatorcontrib><creatorcontrib>Malik, Hamid Ullah</creatorcontrib><creatorcontrib>Fazili, Mujeeb ur Rehman</creatorcontrib><creatorcontrib>Qureshi, Sabia</creatorcontrib><creatorcontrib>Mir, Masood Salim</creatorcontrib><creatorcontrib>Yousuf, Raja Wasim</creatorcontrib><creatorcontrib>Tufani, Noor Alam</creatorcontrib><creatorcontrib>Dhama, Kuldeep</creatorcontrib><creatorcontrib>Bashir, Shah Tauseef</creatorcontrib><title>Comparative evaluation of different therapeutic protocols for contagious caprine pleuropneumonia in Himalayan Pashmina goats</title><title>Tropical animal health and production</title><addtitle>Trop Anim Health Prod</addtitle><addtitle>Trop Anim Health Prod</addtitle><description>Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same leads to the development of antibiotic resistance and decreased efficacy of drug. Besides, inflammatory and allergic pathogenesis of CCPP envisages combination therapy. In this study, we evaluated the effectiveness of the combination therapy using different antibiotics (oxytetracycyline @ 10: group I, enrofloxacin @ 5 group II, and tylosin: group III, @ 10 mg/kg body weight), along with anti-inflammatory (meloxicam @ 0.5 mg/kg) and anti-allergic (pheneramine maleate @ 1.0 mg/kg) drugs. These drugs were given intramuscularly at the interval of 48 h for four times in three test groups ( n  = 10) of Pashmina goats, viz. groups I, II, and III, respectively, affected with CCPP. Group IV ( n  = 10) was kept as healthy control when group V ( n  = 10) treated with oxytetracycline @ 10 mg/kg alone was used as positive control. Clinical signs, clinical parameters, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-α)), and oxidative stress indices (total oxidant status (TOS), total antioxidant status (TAS)) were evaluated at hours 0, 48, 96, and 144 of experimental trial. Tylosin-based combination therapy resulted in a rapid and favorable recovery resulting in restoration of normal body temperature (102.46 ± 0.31 °F), respiration rate (16.30 ± 0.79 per minute), and heart rate (89.50 ± 2.63 per minute) compared to the oxytetracycline (102.95 ± 0.13, 21.30 ± 1.12, 86.00 ± 2.33, respectively) and enrofloxacin (102.97 ± 0.19, 21.00 ± 1.25, 90.00 ± 2.58, respectively) treated groups. By hour 144, all the groups showed restoration of clinical parameters of normal health and diminishing signs of CCPP, viz. fever, dyspnea, coughing, nasal discharge, weakness, and pleurodynia. Significant ( P  ≤ 0.05) decrease in levels of TNF-α and non-significant ( P  &gt; 0.05) decrease in levels of TOS and an increase in levels of TAS were noted from hour 0 to 144 in all the test groups. Within the groups, no significant ( P  &gt; 0.05) change was noted in TNF-α, TOS, and TAS levels; however, TNF-α levels were comparatively lower in group III. Hematological parameters did not differ significantly ( P  &gt; 0.05). From these findings, it can be inferred that tylosin-based combination therapy is relatively better for early, rapid, and safe recovery besides minimizing inflammatory and oxidative cascade in CCPP affected Pashmina goats compared to oxytetracycline- and enrofloxacin-based therapies.</description><subject>Animals</subject><subject>Anti-Allergic Agents - therapeutic use</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antioxidants</subject><subject>Biomedical and Life Sciences</subject><subject>Body temperature</subject><subject>Body weight</subject><subject>Caprinae</subject><subject>Contagious caprine pleuropneumonia</subject><subject>Drug Therapy, Combination - veterinary</subject><subject>Dyspnea</subject><subject>Enrofloxacin</subject><subject>Enrofloxacin - therapeutic use</subject><subject>Female</subject><subject>Fever</subject><subject>Goat Diseases - drug therapy</subject><subject>Goats</subject><subject>Heart rate</subject><subject>India</subject><subject>Inflammation</subject><subject>Life Sciences</subject><subject>Meloxicam</subject><subject>Meloxicam - therapeutic use</subject><subject>Myalgia</subject><subject>Oxidative stress</subject><subject>Oxidizing agents</subject><subject>Oxytetracycline</subject><subject>Oxytetracycline - therapeutic use</subject><subject>Parameters</subject><subject>Pathogenesis</subject><subject>Pheniramine - therapeutic use</subject><subject>Pleuropneumonia</subject><subject>Pleuropneumonia - veterinary</subject><subject>Pleuropneumonia, Contagious - drug therapy</subject><subject>Pneumonia, Mycoplasma</subject><subject>Recovery</subject><subject>Regular Articles</subject><subject>Respiration</subject><subject>Restoration</subject><subject>Therapy</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><subject>Tylosin</subject><subject>Tylosin - therapeutic use</subject><subject>Veterinary Medicine/Veterinary Science</subject><subject>Zoology</subject><issn>0049-4747</issn><issn>1573-7438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU9rFTEUxYMo9rX6BVxIwI2b0fydZJbyqLZQ0IWuQyZz85oyk4xJplDww5vnqwouXIRk8Tsn596D0CtK3lFC1PtCKZOkI3Q4Hso79gTtqFS8U4Lrp2hHiBg6oYQ6Q-el3BHSZLp_js44Jaofhn6HfuzTstpsa7gHDPd23tozRZw8noL3kCFWXG8h2xW2Ghxec6rJpblgnzJ2KVZ7CGkr2Nk1hwh4nWHLaY2wLSkGi0PEV2Gxs32wEX-x5XYJ0eJDsrW8QM-8nQu8fLwv0LePl1_3V93N50_X-w83neNK1m4SAwgnyEid01YLpj1zanKSj4pI6UYxEj6NHjRxI9GOgpNET5PyjnKnFb9Ab0--Lfz3DUo1SygO5tlGaNENY7ztjygpGvrmH_QubTm2dI1iTPdC9LJR7ES5nErJ4E2bfbH5wVBijt2YUzem9WJ-dWNYE71-tN7GBaY_kt9lNICfgHLc5AHy37__Y_sTUDSdEg</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Yatoo, Mohd. 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Iqbal</creatorcontrib><creatorcontrib>Parray, Oveas Raffiq</creatorcontrib><creatorcontrib>Mir, Muheet</creatorcontrib><creatorcontrib>Bhat, Riyaz Ahmed</creatorcontrib><creatorcontrib>Malik, Hamid Ullah</creatorcontrib><creatorcontrib>Fazili, Mujeeb ur Rehman</creatorcontrib><creatorcontrib>Qureshi, Sabia</creatorcontrib><creatorcontrib>Mir, Masood Salim</creatorcontrib><creatorcontrib>Yousuf, Raja Wasim</creatorcontrib><creatorcontrib>Tufani, Noor Alam</creatorcontrib><creatorcontrib>Dhama, Kuldeep</creatorcontrib><creatorcontrib>Bashir, Shah Tauseef</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural &amp; Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Tropical animal health and production</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yatoo, Mohd. Iqbal</au><au>Parray, Oveas Raffiq</au><au>Mir, Muheet</au><au>Bhat, Riyaz Ahmed</au><au>Malik, Hamid Ullah</au><au>Fazili, Mujeeb ur Rehman</au><au>Qureshi, Sabia</au><au>Mir, Masood Salim</au><au>Yousuf, Raja Wasim</au><au>Tufani, Noor Alam</au><au>Dhama, Kuldeep</au><au>Bashir, Shah Tauseef</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative evaluation of different therapeutic protocols for contagious caprine pleuropneumonia in Himalayan Pashmina goats</atitle><jtitle>Tropical animal health and production</jtitle><stitle>Trop Anim Health Prod</stitle><addtitle>Trop Anim Health Prod</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>51</volume><issue>8</issue><spage>2127</spage><epage>2137</epage><pages>2127-2137</pages><issn>0049-4747</issn><eissn>1573-7438</eissn><abstract>Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same leads to the development of antibiotic resistance and decreased efficacy of drug. Besides, inflammatory and allergic pathogenesis of CCPP envisages combination therapy. In this study, we evaluated the effectiveness of the combination therapy using different antibiotics (oxytetracycyline @ 10: group I, enrofloxacin @ 5 group II, and tylosin: group III, @ 10 mg/kg body weight), along with anti-inflammatory (meloxicam @ 0.5 mg/kg) and anti-allergic (pheneramine maleate @ 1.0 mg/kg) drugs. These drugs were given intramuscularly at the interval of 48 h for four times in three test groups ( n  = 10) of Pashmina goats, viz. groups I, II, and III, respectively, affected with CCPP. Group IV ( n  = 10) was kept as healthy control when group V ( n  = 10) treated with oxytetracycline @ 10 mg/kg alone was used as positive control. Clinical signs, clinical parameters, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-α)), and oxidative stress indices (total oxidant status (TOS), total antioxidant status (TAS)) were evaluated at hours 0, 48, 96, and 144 of experimental trial. Tylosin-based combination therapy resulted in a rapid and favorable recovery resulting in restoration of normal body temperature (102.46 ± 0.31 °F), respiration rate (16.30 ± 0.79 per minute), and heart rate (89.50 ± 2.63 per minute) compared to the oxytetracycline (102.95 ± 0.13, 21.30 ± 1.12, 86.00 ± 2.33, respectively) and enrofloxacin (102.97 ± 0.19, 21.00 ± 1.25, 90.00 ± 2.58, respectively) treated groups. By hour 144, all the groups showed restoration of clinical parameters of normal health and diminishing signs of CCPP, viz. fever, dyspnea, coughing, nasal discharge, weakness, and pleurodynia. Significant ( P  ≤ 0.05) decrease in levels of TNF-α and non-significant ( P  &gt; 0.05) decrease in levels of TOS and an increase in levels of TAS were noted from hour 0 to 144 in all the test groups. Within the groups, no significant ( P  &gt; 0.05) change was noted in TNF-α, TOS, and TAS levels; however, TNF-α levels were comparatively lower in group III. Hematological parameters did not differ significantly ( P  &gt; 0.05). From these findings, it can be inferred that tylosin-based combination therapy is relatively better for early, rapid, and safe recovery besides minimizing inflammatory and oxidative cascade in CCPP affected Pashmina goats compared to oxytetracycline- and enrofloxacin-based therapies.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>31076996</pmid><doi>10.1007/s11250-019-01913-2</doi><tpages>11</tpages></addata></record>
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identifier ISSN: 0049-4747
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issn 0049-4747
1573-7438
language eng
recordid cdi_proquest_miscellaneous_2231910754
source MEDLINE; SpringerNature Journals
subjects Animals
Anti-Allergic Agents - therapeutic use
Anti-Bacterial Agents - therapeutic use
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Antibiotic resistance
Antibiotics
Antioxidants
Biomedical and Life Sciences
Body temperature
Body weight
Caprinae
Contagious caprine pleuropneumonia
Drug Therapy, Combination - veterinary
Dyspnea
Enrofloxacin
Enrofloxacin - therapeutic use
Female
Fever
Goat Diseases - drug therapy
Goats
Heart rate
India
Inflammation
Life Sciences
Meloxicam
Meloxicam - therapeutic use
Myalgia
Oxidative stress
Oxidizing agents
Oxytetracycline
Oxytetracycline - therapeutic use
Parameters
Pathogenesis
Pheniramine - therapeutic use
Pleuropneumonia
Pleuropneumonia - veterinary
Pleuropneumonia, Contagious - drug therapy
Pneumonia, Mycoplasma
Recovery
Regular Articles
Respiration
Restoration
Therapy
Tumor necrosis factor-TNF
Tumor necrosis factor-α
Tylosin
Tylosin - therapeutic use
Veterinary Medicine/Veterinary Science
Zoology
title Comparative evaluation of different therapeutic protocols for contagious caprine pleuropneumonia in Himalayan Pashmina goats
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