Search results

Filters

  • Journals
  • Authors
  • Keywords
  • Date
  • Type

Search results

Number of results: 9
items per page: 25 50 75
Sort by:
Download PDF Download RIS Download Bibtex

Abstract

Artemisinin is a powerful antimalarial drug, useful in the treatment of many diseases, includ- ing chickens coccidiosis. Its toxic effects have been well studied in humans and experimental animals, but not sufficiently in broiler chickens. Therefore, in the present study, we aimed to assess the side effects of artemisinin in chickens, by measuring the serum level of proteins and enzymes (ALT, AST, GGT, ALP, CK), by histopathological examination and by the evaluation of relative weight of organs (liver, kidney, heart). Artemisinin was administered in the standard feed for chickens in three different concentrations: 5, 50 and 500 ppm.

Each concentration of artemisinin increased the total serum proteins, gamma-globulins and the serum activity of CK and decreased the serum ALP level. The values of ALT and GGT were higher in the chickens treated with 50 and 500 ppm of artemisinin. Multifocal liver necrosis and inflammatory infiltrate were detected in the chickens that received the 50 and 500 ppm dosage of artemisinin. Minimal tubular necrosis, renal tubular epithelium vacuolation, multifocal interstitial nephritis and mild uric nephrosis were detected in chickens treated with the drug. Artemisinin administration produced no significant changes in the organs relative weight.

Artemisinin, at a concentration of 5 mg/kg of feed is well tolerated by broiler chickens, but the concentrations of 50 and 500 mg/ kg feed can produce toxic effects.

Go to article

Authors and Affiliations

A. Gyӧrke
L.M. Pop
M. Mircean
Z. Kalmár
A.F. Tăbăran
A.I. Paștiu
M.O. Dumitrache
C. Magdaș
A. Balea
D. Bărburaș
V. Mircean
V. Cozma
Download PDF Download RIS Download Bibtex

Abstract

The main objective of this study was to assess the concentration of various minerals (Ca, P, Mg, Cu, Zn, Fe) in the blood of sheep, followed by biochemical analysis in order to reveal possible associations of season and breed. The study was conducted by sampling four herds: Suffolk (n=20), Merino (n=20), Lithuanian blackhead (n=20) and Charolaise (n=7). The first blood collection was conducted in April and the last one was performed in February. The highest level of Ca was estimated in Suffolk ewes, lowest (12.61%) in Merino breed; the highest Mg content was found in Lithuanian blackhead breed, lowest (5.26%) in Charolaise; highest P content was determined in Merino, lowest (24.18%) in Suffolk breed (p<0.05). Evalua- tion of the biochemical parameters during different seasons showed a possible environmental effect on the health of the animals. The difference among minerals content showed the highest level in Ca, Mg, Fe in the autumn, P - in the summer, Cu and Zn - in the winter. The lowest differences between seasons were observed in content of Mg (1.24-4.03% from total average of all seasons) and Ca (0.59-8.18%), the highest – in Cu (2.52-18.36 %) and Zn (4.33-24.33%) (p<0.05). The significance of this work is the possible use of the data in the prevention of metabolic and production diseases.

Go to article

Authors and Affiliations

J. Autukaitė
I. Poškienė
V. Juozaitienė
R. Undzėnaitė
R. Antanaitis
H. Žilinskas
Download PDF Download RIS Download Bibtex

Abstract

The aim of this study was to investigate the impact of heat stress on production performance and oxidative stress in different plumage colors of Japanese quail. For this purpose, a total of 100 birds were used in this study. The 25 birds belonged to Wild-type (n=25, grey), Tuxedo (n=25, black), Golden (n=25, yellow) and Recessive white (n=25). The birds were reared for 42 days in an environmentally controlled room at 39°C and relative humidity of 60-65%. The body weight, body weight gain (g/bird/day), and feed conversion ratio were not different between the groups (p>0.05). However, the feed intake (g/bird/day) of the Wild-type had a higher value than the Tuxedo (black) group counterparts between 15 and 21 days different (p<0.05). There was no significant effect of heat stress on the carcass traits (p>0.05). Spleen weights were different between the groups (p<0.05). The yellow group had the highest spleen weight. The highest MDA level was found in the Recessive White variety, followed by Wild-type (grey), Golden (yellow) and Tuxedo (black), respectively. However, there were no statistical differences amongst the groups (p>0.05). There was also no statistical significance in glutathione (GSH) and superoxide dismutase (SOD) levels (p>0.05). The heat shock protein 70 kDa (HSP70) level was significantly different between the groups (p<0.001). The highest percentage was observed in the Golden (5.06%) and the lowest in the White (1.43%) variety.
There was no superior color variety of Japanese quail regarding fattening performance and carcass traits. It is conceivable that when considering the stress response of the different colors, the Golden group is more sensitive to stress due to the hepatic and cellular level of HSP70.
Go to article

Authors and Affiliations

S. Aslan
1
Y. Baykalir
2
U.G. Simsek
3
B. Gul
4

  1. Dokuz Eylul University, Faculty of Veterinary Medicine, Department of Zootechny, Izmir 35890, Turkey
  2. Balikesir University, Faculty of Veterinary Medicine, Department of Biostatistics, Balikesir 10463, Turkey
  3. Firat University, Faculty of Veterinary Medicine, Department of Animal Science, Elazig 23200, Turkey
  4. Firat University, Faculty of Health Science, Department of Nursing, Elazig 23200, Turkey
Download PDF Download RIS Download Bibtex

Abstract

The aim of the study was to determine biologic variations of the main parameters in cows in early lactation and to compare intra-individual variations of parameters in cows and other species. 50 cows were included in the experiment. Blood samples were taken at the moment of calving, then on 1st, 7th, 14th and 28th day after calving. CVi had the following values: 1.9-5% for MCV, MCH, MCHC, GLU, TProt, ALB, UREA, Ca, P and Mg; 5.1-10% for RBC, Hgb, Hct, WBC, NEU, LYM, BHB, ALT, CHOL, TGC and >10% for PLT, NEFA, TBil, AST and GGT. For RBC, Hgb, Hct, MCV, MCH subject-based reference values or the reference change value should be used. For all other parameters except AST, population-based reference intervals should be used with caution. For LYM, NEU, PLT, GLU, TProt, ALB, CHOL and TGC index of individuality was close to 0.6 which means that subject-based reference values can be much more adequate to use then population-based reference intervals. For AST population-based intervals should be used. There is little effect of parity (increase CVi with parity) and no effect of milk production. CVi values obtained in cows in early lactation are specific because they deviate from the CVi values of other animal species and human. Calculated RCVs varied from 5.5% for MCHC to 41% for AST. High individuality index for many metabolic parameters opens possibility for development of model for longitudinal monitoring of metabolic status of individual animals during lactation. That requires further research.
Go to article

Authors and Affiliations

V. Kovačević
1
M.R. Cincović
1
B. Belić
1
R. Đoković
2
I. Lakić
1
M. Radinović
1
A. Potkonjak
1

  1. Department of Veterinary Medicine, Faculty of Agriculture, University of Novi Sad, Trg D.Obradovića 8, 21000 Novi Sad, Serbia
  2. Faculty of Agronomy, University of Kragujevac, Ul. Cara Dušana 34, 32000 Čačak, Serbia
Download PDF Download RIS Download Bibtex

Abstract

The study was conducted on 26 male, 30 days-old goats, separated from their mothers, divided into two equal groups: I - control and II - experimental, consisting of 13 animals each. All animals were fed with milk replacer, experimental group received additionally 50 g/kg body weight, additive of HMB, for 60 days. The following features were analyzed: body weight, daily increases of body weight, as well as hematological and biochemical blood features. Differences in body weight were found, between experimental and control group, after 60 days of experiment 0.57 kg (p≤0.01). The daily weight gain of experimental animals was higher in comparison with control group. Significant differences were also noted in results of hematological and biochemical blood parameters. Experimental animals showed a higher level of red blood cells as well as number of lymphocytes in comparison with the control group, (p≤0.01).Significant changes were also observed in the level of triglycerides, inorganic phosphorus and protein between both groups. The acid-base balance parameters and ionogram, showed a higher pH level (p≤0.05) HCO – act., HCO – std., BE, ctCO , O sat, K+, Cl– (p≤0.01), while the anion gap (AG) and Na+ were significantly lower in control group (p≤0.01).

Go to article

Authors and Affiliations

K. Cebulska
P. Sobiech
S. Milewski
K. Ząbek
Download PDF Download RIS Download Bibtex

Abstract

The identification of various substances in seminal plasma has opened the way to study their functionality. It was aimed to identify the electrophoretic protein profile (EPP) and biochemical parameters (BP) of seminal plasma (SP) as predictors of semen quality and fertility in stallion. Forty-six ejaculates from 7 fertile stallions, aged between 6-26 years, were collected from May to July and 117 mares were used to obtain fertility data. For each ejaculate, volume, sperm motility, concentration were determined and seminal plasma samples were collected to perform one- -dimensional electrophoresis and biochemical profiling. Following the estrus detection, mares were inseminated with fresh sperm. Pregnancy rates and foal rates were recorded. The concentration of 15-18 kDa molecular weight (MW) proteins has shown a positive correlation with sperm concentration and foal rate. Besides, a strong positive correlation was found between sperm concentration and 23-28 kDa MW proteins (r=0.77). The volume of 19-22 kDa MW proteins was negatively correlated with pregnancy and foal rate. Similarly, the volume of high MW proteins (173-385 kDa) correlated negatively with sperm motility and foal rate. Apart from the protein profile, while Magnesium and Glucose levels were negatively correlated with sperm quality and foal rate, Cholesterol level was a positive indicator of the quality of semen as well as the foaling rate. Moreover, the total protein level was correlated negatively with the sperm concentration whereas triglyceride was correlated positively. In conclusion, EPP and BP of seminal plasma are valuable clinical tools as predictors of fertility and semen quality in the stallion.
Go to article

Bibliography


Akcay E, Reilas T, Andersson M, Katila T (2006) Effect of seminal plasma fractions on stallion sperm survival after cooled storage. J Vet Med A 53: 481-485.

Amann RP, Cristanelli MJ, Squires EL (1985) Proteins in stallion seminal plasma. J Reprod Fertil 35: 113-120.

Argañaraz ME, Apichela SA, Zampini R, Vencato J, Stelletta C (2015) Biochemical and Protein Profile of Alpaca (V icugna pacos) Uterine Horn Fluid During Early Pregnancy. Reprod Domest Anim 50: 121-128.

Ball BA, Gravance CG, Wessel MT, Sabeur K (2003) Activity of Angiotensin-converting enzyme (ACE) in reproductive tissues of the stal-lion and effects of angiotensin II on sperm motility. Theriogenology 59: 901-914.

Brandon CI, Heussner GL, Caudle AB, Fayrer-Hosken RA (1999) Two-dimensional polyacrylamid electrophoresis of equine seminal plasma proteins and their correlation with fertility. Theriogenology 52: 863-873.

Calvete JJ, Mann K, Schafer W, Sanz L, Reinert M, Nessau S, Raida M, Töpfer-Petersen E. (1995) Amino acid sequence of HSP-1, a major protein of stallion seminal plasma: effect of glycosylation on its heparin- and gelatin-binding capabilities. Biochem J 310: 615-622.

Calvete JJ, Nessau S, Mann K, Sanz L, Sieme H, Klug E, Töpfer-Petersen E (1994) Isolation and Biochemical characterization of stallion seminal-plasma proteins. Reprod Domest Anim 29: 411-426.

Carver DA, Ball BA (2002) Lipase activity in stallion seminal plasma and the effect of lipase on stallion spermatozoa during storage at 5 de-grees C. Theriogenology 58: 1587-1595.

Champion ZJ, Vickers MH, Gravance CG, Breier BH, Casey PJ (2002) Growth hormone or insulin-like growth factor-I extends longevity of equine spermatozoa in vitro. Theriogenology 57: 1793-1800.

Cross NL (2003) Decrease in order of human sperm lipids during capacitation. Biol Reprod 69: 529-534.

Costello LC, Franklin R.B. (1991) Concepts of citrate production and secretion by prostate 1. Metabolic relationships. The Prostate 18: 25-46.

Da Ros VG, Maldera JA, Willis WD, Cohen DJ, Goulding EH, Gelman DM, Cuasnicu PS (2008) Impaired sperm fertilizing ability in mice lacking Cysteine-Rich Secretory Protein 1 (CRISP1). Dev Biol, 320: 12-18.

Da Ros VG, Muñoz MW, Battistone MA, Brukman NG, Carvajal G, Curci L, Cuasnicu PS (2015) From the epididymis to the egg: participa-tion of CRISP proteins in mammalian fertilization. Asian J Androl 17: 711-715.

Dias AJ, Maia MS, Retamal CA, Lopez ML (2004) Identification and partial characterization of alpha-1,4-glucosidase activity in equine epi-didymal fluid. Theriogenology 61: 1545-1558.

Doty A, Buhi WC, Benson S, Scoggin KE, Pozor M, Macpherson M, Troedsson MH (2011) Equine CRISP3 modulates interaction between spermatozoa and polymorphonuclear neutrophils. Biol Reprod 85: 157-164.

Druart X, De Graaf S (2018) Seminal plasma proteomes and sperm fertility. Anim Reprod Sci 194: 33-40

Gadella BM, Harrison RA (2002) Capacitation induces cyclic adenosine 3,5-mono-phosphate-dependent, but apoptosis-unrelated, exposure of amino-phospholipids at the apical head plasma membrane of boar sperm cells. Biol Reprod 67: 340-50.

Gebauer MR, Pickett BW, Faulkner LC, Remenga EE, Berndtson WE (1976) Reproductive physiology of the stallion. Chemical characteris-tics of seminal plasma and spermatozoa. J Anim Sci 43: 628-632.

Garcia B, González-Fernández L, Loux SC, Rocha AM, Guimarães T, Pena F.J, Hinrichs K (2015) Effect of calcium, bicarbonate, and albu-min on capacitation-related events in equine sperm. Reproduction 149: 87-99.

Huang YL, Tseng WC, Cheng SY, Lin TH (2007) Trace elements and lipid peroxidation in human seminal plasma. Biol Trace Elem Res 76: 207–215.

Inagaki M, Kikuchi M, Orino K, Ohnami Y, Watanabe K (2002) Purification and quantification of lactoferrin in equine seminal plasma. J Vet Med Sci 64: 75-77.

Jobim MI, Oberst ER, Salbego CG, Souza DO, Wald VB, Tramontina F, Mattos RC (2004) Two-dimensional polyacrylamide gel electrophoresis of bovine seminal plasma proteins and their relation with semen freezability. Theriogenology 61: 255-266.

Jobim MI, Oberst ER, Salbego CG, Wald VB, Horn AP, Mattos RC (2005) BSP A1/A2-like proteins in ram seminal plasma. Theriogenology 63: 2053-2062.

Kareskoski AM, Sankari S, Johannisson A, Kindahl H, Andersson M, Katila T (2011) The association of the presence of seminal plasma and its components with sperm longevity in fractionated stallion ejaculates. Reprod Domest Anim 46: 1073-1081.

Kikuchi M, Mizoroki S, Kubo T, Ohiwa Y, Kubota M, Yamada N, Orino K, Ohnami Y Watanabe K (2003) Seminal plasma lactoferrin but not transferrin reflects gonadal function in dogs. J Vet Med Sci 65: 679-684.

Kosiniak K (1975) Characteristics of the successive jets of ejaculated semen of stallions.” J Reprod Fertil (Suppl) 23: 59-61.

Kosiniak K (1980) The role of the accessory gland secretions during the ejaculate production in stallions. Acta Agrar Silvestria Ser Zootech 2: 75-86.

Kosiniak K, Bittmar A (1981) Biochemical components of stallion seminal plasma before and after the breeding season. Anim Reprod Sci 4: 39-47.

Lackey BR, Gray SL, Henricks DM (2002) Measurement of leptin and insulin-like growth factor-I in seminal plasma from different species. Physiol Res 51: 309-311.

Mann T (1964) The Biochemistry of Semen and of the Male Reproductive Tract, 2nd ed., Methuen & Co press, London, pp 334-337

Mann T (1974) Secretory function of the prostate, seminal vesicle and other male accessory organs of reproduction. J Reprod Fertil 37: 179-188.

Mann T (1975) Biochemistry of stallion semen. J Reprod Fertil (Suppl) 23: 47-52.

Melotti C, Parente R, Di Stasio D, Vitali G, Basunti G, Marchese S, Di Marzio G (1996) Citric acid and fructose seminal plasma concentra-tions and semen characteristics in the stallion. Bioch Clin 20: 90-97.

Novak S, Smith TA, Paradis F, Burwash L, Dyck MK, Foxcroft GR, Dixon WT (2010). Biomarkers of in vivo fertility in sperm and seminal plasma of fertile stallions. Theriogenology 74: 956-967.

Pandy VK, Parmeshwaran M, Soman SD, Dacosta JC (1983) Concentrations of morphologically normal, motile spermatozoa: Mg, Ca and Zn in the semen of infertile men. Sci Total Environ 27: 49-52.

Pesch S, Bergmann M, Bostedt H (2006) Determination of some enzymes and macro-and microelements in stallion seminal plasma and their correlations to semen quality. Theriogenology 66: 307-313.

Pickett BW, Sullivan JJ, Seidel GE Jr (1975) Reproductive physiology of the stallion. V. Effect of frequency of ejaculation on seminal char-acteristics and spermatozoal output. J Anim Sci 40: 917-923.

Restrepo G, Rojano, B, Usuga A (2019). Relationship of cysteine-rich secretory protein-3 gene and protein with semen quality in stallions. Reprod Domest Anim 54: 39-45.

Schambony A, Gentzel M, Wolfes H, Raida M, Neumann U, Töpfer-Petersen E (1998) Equine CRISP-3: primary structure and expression in the male genital tract. Biochim Biophys Acta 1387: 206-216.

Sieber F (1987) Merocyanine 540. Photochem Photobiol 46: 1035-1042.

Stanwell-Smith R, Thompson SG, Haines AP, Ward RJ, Cashmore G, Stedronska J, Hendry W F (1983) A comparative study of zinc, cop-per, cadmium, and lead levels in fertile and infertile men. Fertil Steril 40: 670-677.

Strzezek J, Wysocki P, Kordan W, Kuklinska M, Mogielnicka M, Soliwoda D, Fraser L (2005) Proteomics of boar seminal plasma-current studies and possibility of their application in biotechnology of animal reproduction. Reprod Biol 5: 279-290.

Talluri TR, Mal G, Ravi SK (2017) Biochemical components of seminal plasma and their correlation to the fresh seminal characteristics in Marwari stallions and Poitou jacks. Vet World 10: 214-220.

Tischner M, Kosiniak K, Bielanski W (1974) Analysis of the pattern of ejaculation in stallions. J Reprod Fertil 41: 329-335.

Töpfer-Petersen E, Ekhlasi-Hundrieser M, Kirchhoff C, Leeb T, Sieme H (2005) The role of stallion seminal proteins in fertilisation. Anim Reprod Sci 89: 159-170.

Usuga A, Rojano B, Restrepo G (2017) Effect of seminal plasma components on the quality of fresh and cryopreserved stallion semen. J Equine Vet Sci 58: 103-111.

Varner DD, Schumacher J, Blanchard T, Johnson L (1991) Breeding soundness examination. In: Diseases and management of breeding stallions. American Veterinary Publications, pp 61-96.

Von Fellenberg R, Zweifel HR, Grunig G, Pellegrini A (1985) Proteinase inhibitors of horse seminal plasma. A high molecular mass, ac-id-soluble proteinase inhibitor. Biol Chem Hoppe Seyler 366: 705-712.

Wong WY, Flik G, Groenen PM, Swinkels DW, Thomas CM, Copius-Peereboom JH, Steegers-Theunissen RP (2001) The impact of calcium, magnesium, zinc, and copper in blood and seminal plasma on semen parameters in men. Reprod Toxicol 15: 131-136.
Go to article

Authors and Affiliations

C. Stelletta
1
S. Alberti
2
B. Cil
3
K. Tekin
3
M.B. Tirpan
3
M. Arganaraz
4
E. Akcay
3
A. Daskin
3

  1. Department of Animal Medicine, Production and Health, University of Padova, Agripolis, Viale dell’Università - 35020 Legnaro, Italy
  2. Practitioner, Veneto Region, Italy
  3. Department of Animal Reproduction and Artificial Insemination, Faculty of Veterinary Medicine, Ankara University, 06110, Ankara, Turkey
  4. Instituto Superior de Investigaciones Biológicas (INSIBIO) and Instituto de Biología “Dr. Francisco D. Barbieri”, Facultad de Bioquímica, Química y Farmacia, UNT Chacabuco 461, T4000ILI, San Miguel de Tucumán, Argentina
Download PDF Download RIS Download Bibtex

Abstract

During the transition period, the cow’s body activates adaptive mechanisms aimed at adjusting to the changing demand for energy and nutrients, which are necessary for the growing fetus and the subsequent start of milk production. This time is also associated with an increased risk of metabolic diseases and reproductive disorders.
Our study aimed to identify prepartum and postpartum biochemical markers and weight loss patterns that could differentiate cows that would exhibit ultrasonographic signs of liver fatty infiltration during the latter half of the transition period.
The study was performed in a single herd of Holstein-Friesian cows and the animals were divided into two groups: CON (n=13) – cows without ultrasonographic signs of fatty liver, and FL (n=16) – cows with ultrasonographic signs of fatty liver. Backfat thickness and specific biochemical parameters were measured weekly from one week before parturition to 9 weeks postpartum.
Our study highlights the importance of using a combination of monitoring methods to assess the metabolic status of transition dairy cattle. The results showed that ultrasound measurements of backfat thickness, blood NEFA levels, glucose concentration, and AST activity were all different (p<0.05) between the control and FL groups, indicating the usefulness of these parameters in monitoring the health status of transition cows. Additionally, the results suggest that high prepartum glucose levels (4.99 mmol/l) could serve as a potential marker for future FL, while the elevated NEFA levels (0.51 mmol/l) and decreased AST activity (80.56 u/l) in FL animals indicate their potential as indicators of lipid mobilization and liver structural damage, respectively.
Go to article

Bibliography

1. Abuelo A, Hernández J, Benedito JL, Castillo C (2016) Association of oxidative status and insulin sensitivity in periparturient dairy cat-tle: an observational study. J Anim Physiol Anim Nutr (Berl) 100: 279-286.
2. Akbar H, Grala TM, Vailati Riboni M, Cardoso FC, Verkerk G, McGowan J, Macdonald K, Webster J, Schutz K, Meier S, Matthews L, Roche JR, Loor JJ (2015) Body condition score at calving affects systemic and hepatic transcriptome indicators of inflammation and nu-trient metabolism in grazing dairy cows. J Dairy Sci 98: 1019-1032.
3. Angeli E, Rodríguez FM, Rey F, Santiago G, Matiller V, Ortega HH, Hein GJ (2019) Liver fatty acid metabolism associations with re-productive performance of dairy cattle. Anim Reprod Sci 208: 106104.
4. Aschenbach JR, Kristensen NB, Donkin SS, Hammon HM, Penner GB (2010) Gluconeogenesis in dairy cows: the secret of making sweet milk from sour dough. IUBMB Life 62: 869-877.
5. Bezerra LR, de Oliveira Neto CB, de Araujo MJ, Edvan RL, de Oliveira WD, Pereira FB (2014) Major metabolic diseases affecting cows in transition period. Int J Biol 6: 85-94.
6. Bobe G, Young JW, Beitz DC (2004) Invited review: pathology, etiology, prevention, and treatment of fatty liver in dairy cows. J Dairy Sci 87: 3105-3124.
7. Braun U (2009) Ultrasonography of the liver in cattle. Vet Clin North Am Food Anim Pract 25: 591-609.
8. Brethour JR (1992) The repeatability and accuracy of ultrasound in measuring backfat of cattle. J Anim Sci 70: 1039-1044.
9. Ceciliani F, Lecchi C, Urh C, Sauerwein H (2018) Proteomics and metabolomics characterizing the pathophysiology of adaptive reactions to the metabolic challenges during the transition from late pregnancy to early lactation in dairy cows. J Proteomics 178: 92-106.
10. Contreras GA, Sordillo LM (2011) Lipid mobilization and inflammatory responses during the transition period of dairy cows. Comp Immunol Microbiol Infect Dis 34: 281-289.
11. Esposito G, Irons PC, Webb EC, Chapwanya A (2014) Interactions between negative energy balance, metabolic diseases, uterine health and immune response in transition dairy cows. Anim Reprod Sci 144: 60-71.
12. Gerspach C, Imhasly S, Gubler M, Naegeli H, Ruetten M, Laczko E (2017a) Altered plasma lipidome profile of dairy cows with fatty liver disease. Res Vet Sci 110: 47-59.
13. Gerspach C, Imhasly S, Klingler R, Hilbe M, Hartnack S, Ruetten M (2017b). Variation in fat content between liver lobes and compari-son with histopathological scores in dairy cows with fatty liver. BMC Vet Res 13: 98.
14. Hussein HA, Thurmann JP, Staufenbiel R (2020) 24-h variations of blood serum metabolites in high yielding dairy cows and calves. BMC Vet Res 16: 327.
15. Hussein HA, Westphal A, Staufenbiel R (2013) Relationship between body condition score and ultrasound measurement of backfat thickness in multiparous Holstein dairy cows at different production phases. Aust Vet J 91: 185-189.
16. Jawor P, Brzozowska A, Słoniewski K, Kowalski ZM, Stefaniak T (2016) Acute phase response in the primiparous dairy cows after re-peated percutaneous liver biopsy during the transition period. Pol J Vet Sci 19: 393-399.
17. Jorritsma R, Jorritsma H, Schukken YH, Bartlett PC, Wensing T, Wentink GH (2001) Prevalence and indicators of post partum fatty in-filtration of the liver in nine commercial dairy herds in the Netherlands Livest Prod Sci 68: 53-60.
18. Kida K (2003) Relationships of metabolic profiles to milk production and feeding in dairy cows. J Vet Med Sci 65: 671-677.
19. Komeilian MM, Sakha M, Nadalian MG, Veshkini A (2011) Hepatic ultrasonography of dairy cattle in postpartum period: finding the sonographic features of fatty liver syndrome. Aust J Basic Appl Sci 5: 701-706.
20. Luke TD, Rochfort S, Wales WJ, Bonfatti V, Marett L, Pryce JE.(2019) Metabolic profiling of early-lactation dairy cows using milk mid-infrared spectra. J Dairy Sci 102: 1747-1760.
21. Melendez P, Whitney M, Williams F, Pinedo P, Manriquez D, Moore SG, Lucy MC, Pithua P, Poock SE (2018) Technical note: Evalua-tion of fine needle aspiration cytology for the diagnosis of fatty liver in dairy cattle. J Dairy Sci 101: 4483-4490.
22. Oetzel GR (2007) Herd-level ketosis – diagnosis and risk factors. American Association of Bovine Practitioners 40th Annual Conf., Vancouver, BC 67-97.
23. Ospina PA, Nydam DV, Stokol T, Overton TR (2010) Associations of elevated nonesterified fatty acids and beta-hydroxybutyrate con-centrations with early lactation reproductive performance and milk production in transition dairy cattle in the northeastern United States. J Dairy Sci 93: 1596-1603
24. Pires JA, Delavaud C, Faulconnier Y, Pomiès D, Chilliard Y (2013) Effects of body condition score at calving on indicators of fat and protein mobilization of periparturient Holstein-Friesian cows. J Dairy Sci 96: 6423-6439.
25. Puppel K, Kuczyńska B (2016) Metabolic profiles of cow’s blood; a review. J Sci Food Agric 96: 4321-4328.
26. Raboisson D, Mounié M, Maigné E (2014) Diseases, reproductive performance, and changes in milk production associated with sub-clinical ketosis in dairy cows: a meta-analysis and review. J Dairy Sci 97: 7547-7563.
27. Raschka C, Ruda L, Wenning P, von Stemm CI, Pfarrer C, Huber K, Meyer U, Dänicke S, Rehage J (2016) In vivo determination of subcutaneous and abdominal adipose tissue depots in German Holstein dairy cattle. J Anim Sci 94: 2821-2834.
28. Redfern EA, Sinclair LA, Robinson PA (2021) Dairy cow health and management in the transition period: The need to understand the human dimension. Res Vet Sci 137: 94-101.
29. Reynolds CK, Aikman PC, Lupoli B, Humphries DJ, Beever DE (2003) Splanchnic metabolism of dairy cows during the transition from late gestation through early lactation. J Dairy Sci 86: 1201-1217.
30. Roche JR, Friggens NC, Kay JK, Fisher MW, Stafford KJ, Berry DP (2009) Invited review: Body condition score and its association with dairy cow productivity, health, and welfare. J Dairy Sci 92: 5769-5801.
31. Schröder UJ, Staufenbiel R (2006) Invited review: Methods to determine body fat reserves in the dairy cow with special regard to ultra-sonographic measurement of backfat thickness. J Dairy Sci 89: 1-14.
32. Sejersen H, Sørensen MT, Larsen T, Bendixen E, Ingvartsen KL (2012) Liver protein expression in dairy cows with high liver triglycer-ides in early lactation. J Dairy Sci 95: 2409-2421.
33. Siachos N, Oikonomou G, Panousis N, Banos G, Arsenos G, Valergakis GE (2021) Association of body condition score with ultra-sound measurements of backfat and longissimus dorsi muscle thickness in periparturient Holstein cows. Animals (Basel) 11: 818.
34. Stengärde L, Tråvén M, Emanuelson U, Holtenius K, Hultgren J, Niskanen R (2008) Metabolic profiles in five high-producing Swedish dairy herds with a history of abomasal displacement and ketosis. Acta Vet Scand 50: 31
35. Strieder-Barboza C, Zondlak A, Kayitsinga J, Pires AF, Contreras GA (2015) Lipid mobilization assessment in transition dairy cattle us-ing ultrasound image biomarkers. Livest. Sci 177: 159-164.
36. Stojevic Z, Piršljin J, Milinkovic-Tur S, Zdelar-Tuk M, Ljubic BB (2005) Activities of AST, ALT and GGT in clinically healthy dairy cows during lactation and in the dry period. Vet Arhiv 75: 67-73.
37. Tharwat M (2012) Ultrasonography as a diagnostic and prognostic approach in cattle and buffaloes with fatty infiltration of the liver. Pol J Vet Sci 15: 83-93.
38. Tharwat M, Endoh D, Oikawa S (2012) Hepatocyte apoptosis in dairy cows with fatty infiltration of the liver. Res Vet Sci 93: 1281-1286.
39. van Dorland HA, Richter S, Morel I, Doherr MG, Castro N, Bruckmaier RM (2009) Variation in hepatic regulation of metabolism dur-ing the dry period and in early lactation in dairy cows. J Dairy Sci 92: 1924-1940.
Go to article

Authors and Affiliations

D. Grzybowska
1
P. Sobiech
1
D. Tobolski
1

  1. Department and Clinic of Internal Diseases, Faculty of Veterinary Medicine, University of Warmia and Mazury in Olsztyn, Oczapowskiego 14, 10-957 Olsztyn, Poland
Download PDF Download RIS Download Bibtex

Abstract

François Chapeville (Franciszek Chrapkiewicz), an outstanding Polish biochemist, spent his entire adult life in France. After graduating in veterinary and biochemistry there, he completed a postdoctoral fellowship at the Fritz Lipmann laboratory at Rockefeller University in New York. There, he conducted studies that proved that the genetic information encoded in DNA is deciphered in the process of protein biosynthesis via adapter tRNA molecules (adapter hypothesis). In the years 1979–1991 he was appointed director of Jacques Monod Institute of Molecular Biology at the University VII in Paris. He was a great promoter of Polish-French cooperation in the natural sciences. He passed away in Paris at the age of 96. He was buried in his hometown of Strzyżów in the Podkarpacie region.
Go to article

Authors and Affiliations

Andrzej B. Legocki
1

  1. Instytut Chemii Bioorganicznej PAN, Poznań
Download PDF Download RIS Download Bibtex

Abstract

The article presents personal memories of Professor Aleksander Koj’s alumni. Professor Aleksander Koj was a world-class biochemist of significant scientific achievements, a renowned authority in the field of acute-phase response regulation and acute-phase proteins. He was an excellent academic, a true Master, admired and followed by many Polish biochemists. Thrice he served as the Rector of the Jagiellonian University in Kraków. He navigated the University through a difficult time of political transformation in Poland, modernized the management system of the University and led to the commencement of the construction of the new University campus. He was the co-creator and the first Chairman of the Conference of Rectors of Academic Schools in Poland. He will be remembered as a devoted community worker aiming at strengthening the bond between the Polish community abroad and our homeland, propagating knowledge, promoting the concept of European integration, democracy and tolerance, as well as the collaboration between scientists, artists and men and women of culture. He was wise, righteous, and noble. Many had the honor of calling him their friend, and a great many saw in him a moral authority.

Go to article

Authors and Affiliations

Joanna Bereta
Hanna Rokita

This page uses 'cookies'. Learn more