دورية أكاديمية

Hematological and serum biochemistry evaluation in howler monkeys (Alouatta caraya) and capuchin monkeys (Sapajus apella): A comparative study.

التفاصيل البيبلوغرافية
العنوان: Hematological and serum biochemistry evaluation in howler monkeys (Alouatta caraya) and capuchin monkeys (Sapajus apella): A comparative study.
المؤلفون: da Silva GP; Universidade Federal Rural da Amazônia (UFRA), Programa de Pós-graduação em Saúde e Produção Animal na Amazônia, Belém, Pará, Brazil., Pereira THS; Universidade Federal Rural da Amazônia (UFRA), Programa de Pós-graduação em Saúde e Produção Animal na Amazônia, Belém, Pará, Brazil., de Melo JT; Centro Nacional de Primatas (CENP), Instituto Evandro Chagas (IEC), Ananindeua Pará, Brazil., Imbeloni AA; Centro Nacional de Primatas (CENP), Instituto Evandro Chagas (IEC), Ananindeua Pará, Brazil., Andrade RDS; Centro Nacional de Primatas (CENP), Instituto Evandro Chagas (IEC), Ananindeua Pará, Brazil., Monteiro MVB; Instituto de Ciências Biológicas, Programa de Pós-graduação em Análises Clínicas, Universidade Federal do Pará (UFPA), Belém, Brazil., Monteiro FOB; Universidade Federal Rural da Amazônia (UFRA), Programa de Pós-graduação em Saúde e Produção Animal na Amazônia, Belém, Pará, Brazil., Takeshita RSC; Department of Anthropology, Kent State University, Kent, Ohio, USA.
المصدر: Journal of medical primatology [J Med Primatol] 2023 Jun; Vol. 52 (3), pp. 170-185. Date of Electronic Publication: 2023 Apr 20.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
اللغة: English
بيانات الدورية: Publisher: Wiley Country of Publication: Denmark NLM ID: 0320626 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0684 (Electronic) Linking ISSN: 00472565 NLM ISO Abbreviation: J Med Primatol Subsets: MEDLINE
أسماء مطبوعة: Publication: Copenhagen : Wiley
Original Publication: Basel, New York, Karger.
مواضيع طبية MeSH: Alouatta*/physiology , Alouatta caraya*, Animals ; Cebus ; Sapajus apella ; Erythrocytes
مستخلص: Background: Evaluation of blood parameters in captive non-human primates (NHPs) is crucial for monitoring their health and ensuring that their environment meets their physiological requirements.
Methods: We performed hemogram, serum biochemistry, and parasitological exams in 20 howler monkeys and 21 capuchin monkeys.
Results: In both species, over 50% of the individuals presented at least one parasite. There was a negative effect of age on red blood cell (RBC), white blood cell, platelets, total protein, globulin, and alkaline phosphatase, and a positive effect on the A:G ratio, gamma-glutamyl transferase, and mean platelet volume (MPV). Capuchin monkeys presented the highest platelets and alanine aminotransferase (ALT) values and howler monkeys presented the highest MPV, aspartate aminotransferase, ALT, amylase, glucose, bilirubin, and triglycerides values. We observed an interaction between species and sex on RBC, Htc, mean corpuscular hemoglobin concentration, and cholesterol.
Conclusions: Species differences found in blood parameters may reflect differences in physiological adaptations associated with ecological and morphological traits and are clinically relevant for evaluating animal health and the suitability of breeding programs.
(© 2023 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.)
References: Lee JR, Ryu DS, Park SJ, et al. Successful application of human-based methyl capture sequencing for methylome analysis in non-human primate models. BMC Genomics. 2018;19:1-12. doi:10.1186/s12864-018-4666-1.
Miss FM, Meunier H, Burkart JM. Primate origins of corepresentation and cooperative flexibility: a comparative study with common marmosets (Callithrix jacchus), brown capuchins (Sapajus apella), and Tonkean macaques (Macaca tonkeana). J Comp Psychol. 2022;136:199-212. doi:10.1037/com0000315.
Muniz JACP, Leal LCP, Bahia CP, Krejcová LV. Sapajus apella como modelo para o desenvolvimento de novas abordagens terapêuticas para a doença de Parkinson. Rev Pan-Amaz Saude. 2021;12:e202100514. doi:10.5123/S2176-6223202100514.
Sanchez-Fernandez C, Bolatti EM, Culasso ACA, et al. Identification and evolutionary analysis of papillomavirus sequences in New World monkeys (genera Sapajus and Alouatta) from Argentina. Arch Virol. 2022;167:1257-1268. doi:10.1007/s00705-022-05420-y.
de Melo CMF, Daneze ER, Mendes NS, et al. Genetic diversity and hematological and biochemical alterations in Alouatta primates naturally infected with hemoplasmas in Brazil. Comp Immunol Microbiol Infect Dis. 2019;63:104-111. doi:10.1016/j.cimid.2019.01.011.
Di Fiore A, Campbell CJ. The atelines: variation in ecology, behavior, and social organization. In: Campbell CJ, Fuentes AF, MacKinnon KC, Panger M, Bearder S, eds. Primates in Perspective. 2ª ed. Oxford University Press; 2010:155-185.
Svoboda WK, Malanski LS, Shiozawa MM, et al. Dados biométricos de Alouatta caraya de vida livre de ilhas do alto rio Paraná, Porto Rico, PR. XXVI Congresso Brasileiro de Zoologia. Anais do XXVI Congresso Brasileiro de Zoologia. Sociedade Brasileira de Zoologia. CD-ROM; 2006.
Fleagle JG, Mittermeier RA. Locomotor behavior, body size, and comparative ecology of seven Surinam monkeys. Am J Phys Anthropol. 1980;52:301-314. doi:10.1002/ajpa.1330520302.
Fragaszy DM, Izar P, Liu Q, Eshchar Y, Young LA, Visalberghi E. Body mass in wild bearded capuchins (Sapajus libidinosus): ontogeny and sexual dimorphism. Am J Primatol. 2016;78:473-484. doi:10.1002/ajp.22509.
Milton K. The Foraging Strategy of Howler Monkeys: A Study in Primate Economics. Columbia University Press; 1980:165.
Silver SC, Ostro LE, Yeager CP, Dierenfeld ES. Phytochemical and mineral components of foods consumed by black howler monkeys (Alouatta pigra) at two sites in Belize. Zoo Biol. 2000;19:95-109. doi:10.1002/1098-2361(2000)19:2%3c95::AID-ZOO1%3e3.0.CO;2-D.
Serio-Silva JC, Rico-Gray V, Hernández-Salazar LT, Espinosa-Gómez R. The role of Ficus (Moraceae) in the diet and nutrition of a troop of Mexican howler monkeys, Alouatta palliata mexicana, released on an Island in southern Veracruz. Mexico J Trop Ecol. 2002;18:913-928. doi:10.1017/S0266467402002596.
Izawa K. Foods and feeding behavior of wild black-capped capuchin (Cebus apella). Primates. 1979;20:57-76. doi:10.1007/BF02373828.
Phillips KA, Grafton BW, Haas ME. Tap-scanning for invertebrates by capuchins (Cebus apella). Folia Primatol. 2003;74:162-164. doi:10.1159/000070650.
Gómez-Posada C. Dieta y comportamiento alimentario de un grupo de mico maicero Cebus apella de acuerdo a la variación en la oferta de frutos y artrópodos, en la Amazonía colombiana. Acta Amazon. 2012;42:363-372. doi:10.1590/S0044-59672012000300008.
Wirz A, Truppa V, Riviello MC. Hematological and plasma biochemical values for captive tufted capuchin monkeys (Cebus apella). Am J Primatol. 2008;70:463-472. doi:10.1002/ajp.20520.
Monteiro FOB, Monteiro MVB, Scofield A, Whiteman CW, Alfieri AF, Alfieri AA. Hematological and biochemistry evaluation in capuchin monkeys from the ilegal captivity. Acta Vet Bras. 2016;10:92-97. doi:10.21708/avb.2016.10.1.5487.
Fontana VLDS, de Melo FR, Rezende Júnior SA, et al. Avaliação laboratorial da saúde de macacos prego (Cebus apella) na cidade de Jataí-GO. PUBVET. 2016;10:537-541.
Naves EA, Ferreira FA, Mundim AV, Guimarães EC. Valores hematológicos de macaco prego (Cebus apella-Linnaeus, 1758) em cativeiro. Biosci J. 2006;22:125-131.
Flaiban KKMC, Spohr KAH, Malanski LS, et al. Valores hematológicos de bugios pretos (Alouatta caraya) de vida livre da região do Alto Rio Paraná, sul do Brasil. Arq Bras Med Vet Zootec. 2008;61:628-634. doi:10.1590/S0102-09352009000300016.
de Melo CMF, Daneze ER, Morales AD, Sobreira MFR. Evaluación de los parámetros hematológicos, bioquímica sérica y electroforesis de proteínas séricas de primates (Alouatta caraya) en cautiverio en el Estado de São Paulo. Brasil Rev Vet Zootec. 2019;13:45-56. doi:10.17151/vetzo.2019.13.1.3.
Gonçalves GHP, de Souza Junior JC, Pitz HDS, Peruchi AR, Branco FS, Hirano ZMB. Hematological and serum biochemistry data on southern brown howler monkeys (Alouatta guariba clamitans) in captivity in Brazil. J Med Primatol. 2019;48:313-319.
Takeshita RSC, Monteiro FOB, Lins FLML, et al. Hematological, hepatic, and renal evaluation in Aotus azarai infulatus. J Med Primatol. 2011;40:104-110. doi:10.1111/j.1600-0684.2010.00452.x.
Cardoso DL, Costa SM, Muniz JAPC, de Castro PHG, da Costa JB, Dias HLT. Avaliação do perfil hematológico e bioquímico de macacos de cheiro (Saimiri collinsi) cativos no Centro Nacional de Primatas no Estado do Pará. Braz J Anim Environ Res. 2021a;4:2764-2776. doi:10.34188/bjaerv4n2-097.
Cardoso DL, Costa SM, Espinheiro RF, de Castro PHG, Dias HLT. Perfil hematológico e bioquímico de primatas não humanos (Callithrix penicillata) cativos no Centro Nacional de Primatas no Estado do Pará. Biotemas. 2021;34:1-9. doi:10.5007/2175-7925.2021.e82367.
Silva IO, da Silva FFR, Fuzessy LF, et al. Hematology and blood biochemistry in wild hybrid marmosets from the Atlantic Forest. Brazil Cienc Rural. 2014;44:1596-1602. doi:10.1590/0103-8478cr20120822.
Rovirosa-Hernández MJ, Rodríguez-Landa JF, García-Orduña F, et al. Hematologic reference intevals for spider monkeys (Ateles geoffroyi) in managed care with respect to sex and age. J Zoo Wildl Med. 2022;53:214-221. doi:10.1638/2018-0128.
Chung SH, Chang LW, Cheng TL, Lin CJ, Chen WY, Chou CC. Establishing in-house reference intervals for dogs in veterinary clinics. Taiwan Vet J. 2016;42:53-67. doi:10.1142/S1682648515500225.
da Silva GP, Pereira THS, Imbeloni AA, et al. Effect of age and sex in renal function by ultrasound and serum chemistry in two primate species (Alouatta caraya and Sapajus apella). J Med Primatol. 2022;51:223-233. doi:10.1111/jmp.12599.
Willis HH. Simple levitation method for the detection of hookworm ova. Med J Aust. 1921;8:375-376. doi:10.5694/j.1326-5377.1921.tb60654.x.
Hoffman WA, Pons JA, Janer JL. The sedimentation concentration method in Schistosoma mansoni. PR J Public Health Trop Med. 1934;9:283-291.
Levene H. Robust tests for equality of variances. In: Olkin I, ed. Contributions to Probability and Statistics, vol. 1. Stanford University Press; 1960:278-292.
Box GEP, Cox DR. An analysis of transformations. J R Soc. 1964;26:211-252.
Burnham KP, Anderson DR. Model Selection and Multimodel Inference. A Practical Information-Theoretic Approach. Springer; 2002:488.
García-Feria LM, Chapman CA, Pastor-Nieto R, Serio-Silva JC. Biochemical and hematological evaluations of black howler monkeys (Alouatta pigra) in highly degraded landscapes in Mexico. J Med Primatol. 2017;46:304-310. doi:10.1111/jmp.12286.
Canales-Espinosa D, Jesus Rovirosa-Hernández M, Thoisy B, Caba M, García-Orduña F. Hematology and serum biochemistry in wild howler monkeys. In: Kowalewski MM, Garber PA, Cortés-Ortiz L, Urbani B, Youlatos D, eds. Howler Monkeys. Developments in Primatology: Progress and Prospects. Springer; 2015:179-202. doi:10.1007/978-1-4939-1957-4_7.
Favareto AD, Costa MM, Grumann MR, et al. Perfil hematológico e bioquímico de macacos-prego (Cebus spp.) mantidos em cativeiro. Rev Bras Med Vet. 2016;38:406-412.
Monteiro FOB, Coutinho LN, Araújo KF, et al. Biochemical and haematological parameters in owl monkeys infected and uninfected with Trypanoxyuris sp. J Helminthol. 2009;83:225-229. doi:10.1017/S0022149X08156772.
Ellwanger JH, Kulmann-Leal B, Kaminski VL, et al. Beyond diversity loss and climate change: impacts of Amazon deforestation on infectious diseases and public health. An Acad Bras Cienc. 2020;92:e20191375.
Chilvers BL, Cowan PE, Waddington DC, Kelly PJ, Brown TJ. The prevalence of infection of Giardia spp. and Cryptosporidium spp. in wild animals on farmland, southeastern North Island, New Zealand. Int J Environ Health Res. 1998;8:59-64. doi:10.1080/09603129873660.
Einarsson E, Ma'ayeh S, Svärd SG. An up-date on Giardia and giardiasis. Curr Opin Microbiol. 2016;34:47-52. doi:10.1016/j.mib.2016.07.019.
Volotao ACC, Souza Júnior JC, Grassini C, Peralta JM, Fernandes O. Genotyping of Giardia duodenalis from southern brown howler monkeys (Alouatta clamitans) from Brazil. Vet Parasitol. 2008;158:133-137. doi:10.1016/j.vetpar.2008.07.003.
Ryan U, Zahedi A. Molecular epidemiology of giardiasis from a veterinary perspective. Giardia and Giardiasis. 2019;106:209-254. doi:10.1016/bs.apar.2019.07.002.
Li J, Wang H, Wang R, Zhang L. Giardia duodenalis infections in humans and other animals in China. Front Microbiol. 2017;8:2004. doi:10.3389/fmicb.2017.02004.
Zhong Z, Tian Y, Li W, et al. Multilocus genotyping of Giardia duodenalis in captive nonhuman primates in Sichuan and Guizhou provinces, Southwestern China. PLoS One. 2017;12:e0184913. doi:10.1371/journal.pone.0184913.
Ortega YR, Eberhard ML. Protozoan diseases: cryptosporidiosis, giardiasis and other intestinal protozoan diseases. International Encyclopedia of Public Health. Elsevier Academic Press; 2008:354-366. doi:10.1016/b978-012373960-5.00485-8.
Wanger A, Chavez V, Huang RSP, Wahed A, Actor JK, Dasgupta A. Infections caused by parasites. In: Wanger A, Chavez V, Huang RSP, Wahed A, Dasgupta A, Actor JK, eds. Microbiology and Molecular Diagnosis in Pathology. Elsevier Academic Press; 2017:191-219. doi:10.1016/b978-0-12-805351-5.00010-7.
Petrášová J, Modrý D, Huffman MA, et al. Gastrointestinal parasites of indigenous and introduced primate species of Rubondo Island National Park. Tanzania Int J Primatol. 2010;31:920-936. doi:10.1007/s10764-010-9439-x.
Regan CS, Yon L, Hossain M, Elsheikha HM. Prevalence of Entamoeba species in captive primates in zoological gardens in the UK. PeerJ. 2014;29(2):e492. doi:10.7717/peerj.492.
Chinchilla M, Guerrero O, Gutiérrez-Espeleta G, Sánchez R, Valerio I. Parásitos en monos carablanca Cebus capucinus (Primates: Cebidae) de Costa Rica. Parasitol Latinoam. 2007;62:170-175. doi:10.4067/S0717-77122007000200011.
Rondón S, Ortiz M, León C, Galvis N, Link A, González C. Seasonality, richness and prevalence of intestinal parasites of three neotropical primates (Alouatta seniculus, Ateles hybridus and Cebus versicolor) in a fragmented forest in Colombia. Int J Parasitol Parasites Wildl. 2017;6:202-208. doi:10.1016/j.ijppaw.2017.07.006.
Carmo AM, Salgado CA. Ocorrência de parasitos intestinais em Callithrix sp. (Mammalia, Primates, Callithrichidae) Rev Bras Zoociênc. 2003;5:267-262.
Alcântara DS, Mendonça IL, Fernandes Neto VP, Carniel PG, Pessoa FB. Estudo coproparasitológico da espécie Cebus libidinosus (macaco-prego). Arq Bras Med Vet Zootec. 2016;68:1609-1612.
Andrade A, Pinto SC, Oliveira RS. Animais de Laboratório: criação e experimentação. Editora FIOCRUZ; 2002:388.
Harman R, Mason P. Handbook of Pharmacy Healthcare: Diseases and Patient Advice. Pharmaceutical Press; 2002:608.
Parr NA, Fedigan LM, Kutz SJ. A coprological survey of parasites in white-faced capuchins (Cebus capucinus) from sector Santa Rosa, ACG, Costa Rica. Folia Primatol. 2013;84:102-114. doi:10.1159/000348287.
Barutzki D, Schaper R. Results of parasitological examinations of faecal samples from cats and dogs in Germany between 2003 and 2010. Parasitol Res. 2011;109:S45-S60. doi:10.1007/s00436-011-2402-8.
Mati VL, Raso P, de Melo AL. Strongyloides stercoralis infection in marmosets: replication of complicated and uncomplicated human disease and parasite biology. Parasites Vectors. 2014;7:579.
Li WC, Ying M, Gong PT, et al. Pentatrichomonas hominis: prevalence and molecular characterization in humans, dogs, and monkeys in Northern China. Parasitol Res. 2016;115:569-574. doi:10.1007/s00436-015-4773-8.
Barratt J, Gough R, Stark D, Ellis J. Bulky trichomonad genomes: encoding a Swiss Army knife. Trends Parasitol. 2016;32:783-797.
Santos CS, de Jesus VLT, McIntosh D, et al. Morphological, ultrastructural, and molecular characterization of intestinal tetratrichomonads isolated from non-human primates in southeastern Brazil. Parasitol Res. 2017;116:2479-2488.
Inoue T, Hayashimoto N, Yasuda M, Sasaki E, Itoh T. Pentatrichomonas hominis in laboratory-bred common marmosets. Exp Anim. 2015;64:363-368. doi:10.1538/expanim.15-0010.
Núñez H, Araya M, Cisternas F, et al. Blood biochemical indicators in young and adult Cebus apella of both sexes. J Med Primatol. 2008;37:12-17. doi:10.1111/j.1600-0684.2007.00215.x.
Ferreira AF, Queiroga FL, Mota RA, et al. Hematological profile of captive bearded capuchin monkeys (Sapajus libidinosus) from Northeastern Brazil. Cienc Rural. 2018;48:e20180065. doi:10.1590/0103-8478cr20180065.
Price EA. Aging and erythropoiesis: current state of knowledge. Blood Cells Mol Dis. 2008;41:158-165. doi:10.1016/j.bcmd.2008.04.005.
Bain BJ, Clark DM, Wilkins BS. Bone Marrow Pathology. 4th ed. John Wiley & Sons; 2019. doi:10.1002/9781119398929.
Rovirosa-Hernández MJ, Caba M, García-Orduña F, López-Muñoz JJ, Canales-Espinosa D, Hermida-Lagunes J. Hematological and biochemical blood values in wild populations of black howler monkeys (Alouatta pigra) of Campeche. México J Med Primatol. 2012;41:309-316. doi:10.1111/j.1600-0684.2012.00559.x.
Larsson MHMA, Birgel EH, Benesi FJ, et al. Hematological values of Cebus apella anesthetized with ketamine. Braz J Vet Res Anim Sci. 1999;36:131-135. doi:10.1590/S1413-95961999000300005.
Lima DBC, dos Santos KMM, de Almeida HM, Nascimento CB, Conde Júnior AM, Rizzo MS. Avaliação do perfil hematológico, bioquímico e esfregaço de sangue periférico com vistas ao perfil sanitário em primatas do gênero Cebus mantidos em cativeiro. Semin Cienc Agrar. 2014;35:1847-1854. doi:10.5433/1679-0359.2014v35n4p1847.
Grau M, Cremer JM, Schmeichel S, Kunkel M, Bloch W. Comparisons of blood parameters, red blood cell deformability and circulating nitric oxide between males and females considering hormonal contraception: a longitudinal gender study. Front Physiol. 2018;9:1-12. doi:10.3389/fphys.2018.01835.
Jain NC. Essentials of Veterinary Hematology. Lippincott Williams & Wilkins; 1995:420.
Zeng SM, Yankowitz J, Widness JA, Strauss RG. Etiology of differences in hematocrit between males and females: sequence-based polymorphisms in erythropoietin and its receptor. J Gend Specif Med. 2001;4:35-40.
Veldhuis-Vlug AG, Rosen CJ. Clinical implications of bone marrow adiposity. J Intern Med. 2018;283:121-139. doi:10.1111/joim.12718.
Yu KR, Espinoza DA, Wu C, et al. The impact of aging on primate hematopoiesis as interrogated by clonal tracking. Blood. 2018;131:1195-1205. doi:10.1182/blood-2017-08-802033.
Dimitrov S, Lange T, Born J. Selective mobilization of cytotoxic leukocytes by epinephrine. J Immunol. 2009;184:503-511. doi:10.4049/jimmunol.0902189.
Poitout-Belissent FM, McCartney JE. Interpretation of hematologic data in preclinical toxicological studies. In: Weiss DJ, Wardrop KJ, eds. Schalm's Veterinary Hematology. Wiley-Blackwell; 2010:78-84.
Tao Z, Zhu H, Zhang J, Huang Z, Xiang Z, Hong T. Recent advances of eosinophils and its correlated diseases. Front Public Health. 2022;25(10):1-10. doi:10.3389/fpubh.2022.954721.
Pérez-Brígido CD, Romero-Salas D, Cruz-Romero A, et al. Hematological and biochemical profile of spider monkey (Ateles geoffroyi Kuhl) in captivity. Agro Productividad. 2021;14:1-7. 10.32854/agrop.v14i6.1974.
Ribeiro CLB, de Melo-Reis PR, Lemes SR, de Araújo LA, da Silva-Júnior NJ. Análise hematológica de macacos-prego (Sapajus libidinosus Spix, 1923) e bugios (Alouatta caraya Humboldt, 1812) de vida livre no sul do estado de Tocantins. Brasil Rev Bras Boci. 2015;13:110-114.
Castro J, Puente P, Martínez R, et al. Measurement of hematological and serum biochemical normal values of captive housed Chlorocebus aethiops sabaeus monkeys and correlation with the age. J Med Primatol. 2016;45:12-20. doi:10.1111/jmp.12203.
Koo BS, Lee DH, Kang P, et al. Reference values of hematological and biochemical parameters in young-adult cynomolgus monkey (Macaca fascicularis) and rhesus monkey (Macaca mulatta) anesthetized with ketamine hydrochloride. Lab Anim Res. 2019;35:7. doi:10.1186/s42826-019-0006-0.
Sloan A, Gona P, Johnson A. Cardiovascular correlates of platelet count and volume in the Framingham heart study. Ann Epidemiol. 2015;25:492-498. doi:10.1016/j.annepidem.2015.01.010.
Ittermann T, Feig MA, Petersmann A, et al. Mean platelet volume is more important than age for defining reference intervals of platelet counts. PLoS One. 2019;14:e0213658. doi:10.1371/journal.pone.0213658.
Berlin G, Hammar M, Tapper L, Tynngård N. Effects of age, gender and menstrual cycle on platelet function assessed by impedance aggregometry. Platelets. 2019;30:473-479. doi:10.1080/09537104.2018.1466387.
Cardoso DL, Guimarães DAA, Mayor P, et al. Reproductive biology of owl (Aotus spp.) and capuchin (Sapajus spp.) monkeys. Anim Reprod Sci. 2021c;227:1-13. doi:10.1016/j.anireprosci.2021.106732.
Kugelmeier T, do Valle RR, Guimarães MABV, Muniz JAPC, Monteiro FOB, de Oliveira CA. Tracking the ovarian cycle in black-and-gold howlers (Alouatta caraya) by measuring fecal steroids and observing vaginal bleeding. Int J Primatol. 2011;32:605-615. doi:10.1007/s10764-010-9490-7.
Abreu Sousa G, Paludo GR, Teixeira DS, Ribeiro BM. Haematological and biochemical parameters of wild capuchin monkeys in Brasília. Federal District-Brazil J med Primatol. 2020;49:211-217. doi:10.1111/jmp.12468.
Barnard MR, Krueger LA, Frelinger AL III, Furman MI, Michelson AD. Whole blood analysis of leukocyte-platelet aggregates. Curr Protoc Cytom. 2003;6.15:1-8. doi:10.1002/0471142956.cy0615s24 Chapter 6.
Bancroft AJ, Abel EW, Mclaren M, Belch JJ. Mean platelet volume is a useful parameter: a reproducible routine method using a modified coulter thrombocytometer. Platelets. 2000;11:379-387. doi:10.1080/09537100020008311.
Karolczak K, Soltysik B, Kostka T, Witas PJ, Watala C. Platelet and red blood cell counts, as well as the concentrations of uric acid, but not homocysteinaemia or oxidative stress, contribute mostly to platelet reactivity in older adults. Oxid Med Cell Longev. 2019;2019:1-16. doi:10.1155/2019/9467562.
Thompson CB, Jakubowski JA. The pathophysiology and clinical relevance of platelet heterogeneity. Blood. 1988;72:1-8. doi:10.1182/blood.V72.1.1.1.
Korniluk A, Koper-Lenkiewicz OM, Kamińska J, Kemona H, Dymicka-Piekarska V. Mean platelet volume (MPV): new perspectives for an old marker in the course and prognosis of inflammatory conditions. Mediators Inflamm 2019;2019:9213074. doi: 10.1155/2019/9213074.
Rodríguez KH, Navarrete MZ, Lí OE, et al. Valores hematológicos y de bioquímica sérica del mono choro común (Lagothrix lagotricha) criado en semicautiverio en el trópico peruano. Rev Investig Vet Perú. 2014;25:162-170.
Paredes Escobar MR. Valores de bioquímica sanguinea en atélidos de los géneros (Lagothrix y Ateles) en cautiverio en la provincia de pastaza. Cevallos. Proyecto de Investigación [grado de Médico Veterinario Zootecnista]. Universidad Técnica de Ambato; 2020:36.
Videan EN, Fritz J, Murphy J. Effects of aging on hematology and serum clinical chemistry in chimpanzees (pan troglodytes). Am J Primatol. 2008;70:327-338. doi:10.1002/ajp.20494.
Cray C. Acute phase proteins in animals. Prog Mol Biol Transl Sci. 2012;105:113-150. doi:10.1016/B978-0-12-394596-9.00005-6.
Cerón JJ, Eckersall PD, Martınez-Subiela S. Acute phase proteins in dogs and cats: current knowledge and future perspectives. Vet Clin Pathol. 2005;34:85-99.
Ehlting C, Wolf SD, Bode JG. Acute-phase protein synthesis: a key feature of innate immune functions of the liver. Biol Chem. 2021;402:1129-1145. doi:10.1515/hsz-2021-0209.
Pratt DS, Kaplan MM. Evaluation of abnormal liver-enzyme results in asymptomatic patients. N Engl J Med. 2000;342:1266-1271. doi:10.1056/NEJM200004273421707.
Kim WR, Flamm SL, Di Bisceglie AM, Bodenheimer HC. Public Policy Committee of the American Association for the Study of Liver Diseases. Serum activity of alanine aminotransferase (ALT) as an indicator of health and disease. Hepatology. 2008;47:1363-1370. doi:10.1002/hep.22109.
Mukherjee S, Gollan JL. Assessment of liver function. In: Dooley JS, Lok ASF, Burroughs AK, Heathcote EJ, eds. Sherlock's Diseases of the Liver and Biliary System. Blackwell Publishing; 2011:20-35. doi:10.1002/9781444341294.ch2.
Muchlinski MN, Hemingway HW, Pastor J, Omstead KM, Burrows AM. How the brain may have shaped muscle anatomy and physiology: a preliminary study. Anat Rec (Hoboken). 2018;301:528-537. doi:10.1002/ar.23746.
Roth G, Dicke U. Evolution of the brain and intelligence in primates. Prog Brain Res. 2012;195:413-430. doi:10.1016/B978-0-444-53860-4.00020-9.
Hartwig W, Rosenberger AL, Norconk MA, Owl MY. Relative brain size, gut size, and evolution in New World monkeys. Anat Rec (Hoboken). 2011;294:2207-2221. doi:10.1002/ar.21515.
Aiello LC, Wheeler P. The expensive-tissue hypothesis: the brain and the digestive system in human and primate evolution. Curr Anthropol. 1995;36:199-221. doi:10.1086/204350.
Lassen ED. Considerações sobre interpretação de resultados laboratoriais. In: Thrall MA, Baker DC, Campbell TW, et al., eds. Hematologia e bioquímica clínica veterinária. 2nd ed. Roca; 2007:43-50.
Aberkane H, Stoltz JF, Galteau MM, Wellman M. Erythrocytes as targets for gamma-glutamyltranspeptidase initiated pro-oxidant reaction. Eur J Haematol. 2002;68:262-271. doi:10.1034/j.1600-0609.2002.01636.x.
Koenig G, Seneff S. Gamma-glutamyltransferase: a predictive biomarker of cellular antioxidant inadequacy and disease risk. Dis Markers 2015;2015:818570. doi: 10.1155/2015/818570.
Guimarães VY, Justo AA, dos Santos B, Ramos MM, Takahira RK. Serum biochemistry panel of free-living red-handed howler monkeys (Alouatta belzebul) in the eastern Amazon. J Med Primatol. 2022;51:27-32. doi:10.1111/jmp.12556.
Barrett KE, Barman SM, Boitano S, Brooks H. Ganong's Review of Medical Physiology. 24th ed. McGraw-Hill; 2012:768.
Fernandez NJ, Kidney BA. Alkaline phosphatase: beyond the liver. Vet Clin Pathol. 2007;36:223-233. doi:10.1111/j.1939-165x.2007.tb00216.x.
Hinds TD, Stec DE. Bilirubin, a cardiometabolic signaling molecule. Hypertension. 2018;72:788-795.
Wagner JE, Kavanagh K, Ward GM, Auerbach BJ, Harwood HJ Jr, Kaplan JR. Old world nonhuman primate models of type 2 diabetes mellitus. ILAR J. 2006;47:259-271. doi:10.1093/ilar.47.3.259.
Palermo NE, Gianchandani RY, McDonnell ME, Alexanian SM. Stress hyperglycemia during surgery and anesthesia: pathogenesis and clinical implications. Curr Diab Rep. 2016;16:33. doi:10.1007/s11892-016-0721-y.
Pastor-Nieto R. Health and welfare of howler monkeys in captivity. In: Kowalewski M, Garber P, Cortés-Ortiz L, Urbani B, Youlatos D, eds. Howler Monkeys. Developments in Primatology: Progress and Prospects. Springer; 2015:313-355. doi:10.1007/978-1-4939-1960-4_12.
Arroyo-Rodríguez V, Dias PAD. Effects of habitat fragmentation and disturbance on howler monkeys: a review. Am J Primatol. 2010;72:1-16. doi:10.1002/ajp.20753.
Akinfemiwa O, Muniraj T. Amylase. In: StatPearls [Internet]. StatPearls Publishing; 2022:2022 Available from:https://www.ncbi.nlm.nih.gov/books/NBK557738/.
McLeod KR, Baldwin RL, Harmon DL, Richards CJ, Rumpler WV. Influence of ruminal and postruminal starch infusion on energy balance in growing steers. In: Chwalibog A, Jakobsen K, eds. Energy Metabolism in Animals. Wageningen Press; 2001:385-388.
Campos SDE, Stadler RA, Hennemann C, et al. Pancreatite aguda necrótica em bugio-ruivo (Alouatta guariba clamitans) macho adulto. Arq Bras Med Vet Zootec. 2010;62:1280-1284. doi:10.1590/S0102-09352010000500037.
Karastergiou K, Smith SR, Greenberg AS, Fried SK. Sex differences in human adipose tissues-the biology of pear shape. Biol Sex Differ. 2012;3:13. doi:10.1186/2042-6410-3-13.
Plavcan JM, van Schaik CP. Intrasexual competition and body weight dimorphism in anthropoid primates. Am J Phys Anthropol. 1999;103:37-68. doi:10.1002/(SICI)1096-8644(199705)103:1<37::AID-AJPA4>3.0.CO;2-A.
Edwards W, Lonsdorf EV, Pontzer H. Total energy expenditure in captive capuchins (Sapajus apella). Am J Primatol. 2017;79(5):e22638. doi:10.1002/ajp.22638.
Cox RA, García-Palmieri MR. Cholesterol, triglycerides, and associated lipoproteins. In: Walker HK, Hall WD, Hurst JW, eds. Clinical Methods: The History, Physical, and Laboratory Examinations. 3rd ed. Butterworths; 1990:153-160.
Grand TI. Body weight: its relation to tissue composition, segment distribution, and motor function. I. Interspecific comparisons. Am J Phys Anthropol. 1977;47:211-240. doi:10.1002/ajpa.1330470204.
Chivers DJ. Functional anatomy of the gastrointestinal tract. In: Davies AG, Oates JF, eds. Colobine Monkeys: Their Ecology, Behaviour and Evolution. Cambridge University Press; 1994:205-227.
Anapol F, Lee S. Morphological adaptation to diet in platyrrhine primates. Am J Phys Anthropol. 1994;94:239-261. doi:10.1002/ajpa.1330940208.
فهرسة مساهمة: Keywords: hemogram; non-human primates; platyrrhines; serum chemistry
تواريخ الأحداث: Date Created: 20230420 Date Completed: 20230515 Latest Revision: 20230622
رمز التحديث: 20240628
DOI: 10.1111/jmp.12644
PMID: 37078442
قاعدة البيانات: MEDLINE
الوصف
تدمد:1600-0684
DOI:10.1111/jmp.12644