Digital Cushion Fatty Acid Composition and Lipid Metabolism Gene Network Expression in Holstein Dairy Cows Fed a High-Energy Diet

Published on: 10/28/2016
Author/s : Zeeshan Muhammad Iqbal 1; Haji Akbar 2; Afshin Hosseini 1; Elena Bichi Ruspoli Forteguerri 3; Johan S. Osorio 4; Juan J. Loor 1. / 1 Department of Animal Sciences and Division of Nutritional Sciences, University of Illinois, Urbana, Illinois, USA; 2 Department of Biosciences COMSATS Institute of Information Technology, Islamabad, Pakistan; 3 Veterinary Clinical Medicine, University of Illinois, Urbana, Illinois, USA; 4 Department of Dairy Science, South Dakota State University, Brookings, South Dakota, USA
Summary

The hoof digital cushion is a complex structure composed of adipose tissue beneath the distal phalanx, i.e. axial, middle and abaxial fat pad. The major role of these fat depots is dampening compression of the corium underneath the cushion. The study aimed to determine expression of target genes and fatty acid profiles in the hoof of non-pregnant dry Holstein cows fed low (CON) or high-energy (OVE) diets. The middle fat pad of the hoof digital cushion was collected soon after slaughter. Despite the lack of effect on expression of the transcription regulators SREBF1 and PPARG, the expression of the lipogenic enzymes ACACA, FASN, SCD, and DGAT2 was upregulated with OVE. Along with the upregulation of G6PD and IDH1, important for NADPH synthesis during lipogenesis, and the basal glucose transporter SLC2A1, these data indicated a pro-lipogenic response in the digital cushion with OVE. The expression of the lipid droplet-associated protein PLIN2 was upregulated while expression of lipolytic enzymes (ATGL, ABDH5, and LIPE) only tended to be upregulated with OVE. Therefore, OVE induced lipogenesis, lipid droplet formation, and lipolysis, albeit to different extents. Although concentration of monounsaturated fatty acids (MUFA) did not differ, among the polyunsaturated fatty acids (PUFA), the concentration of 20:5n3 was lower with OVE. Among the saturated fatty acids, 20:0 concentration was greater with OVE. Although data indicated that the hoof digital cushion metabolic transcriptome is responsive to higher-energy diets, this did not translate into marked differences in the fatty acid composition. The decrease in concentration of PUFA, which could contribute to synthesis of inflammatory molecules, in OVE-fed cows indicated that feeding higher-energy diets might be detrimental for the mediation of inflammation in digital cushion. This effect could be further exacerbated by physiologic and endocrine changes during the peripartal period that favor inflammation.

Introduction

Lameness is one of the most important welfare issues of high-producing dairy cows in North America [1]. The latter has been attributed to management and environmental factors [2] as well as physiologic adaptations such as postpartal negative energy balance, which can lead cows to excessive loss of body condition (BCS) [3]. Postpartal negative energy balance can be exacerbated by prepartal high-energy diets, where overconditioned cows entering a new lactation mobilize greater amounts of fatty acids (FA) from fat depots such as subcutaneous and mesenteric. The excessive FA mobilization may also affect other lipid-rich tissues such as the digital cushion (i.e., the complex structure located underneath the distal phalanx of the claw) by reducing its thickness and consequently compromising its shock-absorbing capacity [4]. A recent study demonstrated a steady decrease in digital cushion mass from calving to 120 d postpartum, at which point its thickness reached the lowest point during lactation [3]. A lower BCS at calving has been associated with reduced thickness of the digital cushion and, in turn, this condition can lead to development of hoof-related diseases such as sole ulcers and white line disease [3].

Differences between perirenal and subcutaneous adipose depots and the digital cushion have been reported [4], where digital cushion not only had lower lipid content but also higher concentrations of monounsaturated (MUFA) than saturated (SFA) FA with the opposite reported for perirenal and mesenteric fat. The authors attributed these effects to the fundamental differences between tissues, i.e. digital cushion vs. adipose tissues, where the lower lipid content in digital cushion denotes a more protective “cushioning” function for the very sensitive corium to the pressure exerted between the horn and the bone. Those functions contrast the well-established energy storage function of adipose tissues [4]. Despite the fact that the digital cushion thickness decreases through early lactation [3], the effect of dietary energy concentration on digital cushion thickness and risk for lameness remains unknown.

Although there is a considerable amount of data at a transcriptomic level regarding the effects of plane of dietary energy [5] on physiologic adaptations during the peripartal period [6] in subcutaneous adipose tissue, there is a lack of transcriptomic data for the digital cushion. Important transcription factors such as peroxisome proliferator-activated receptors (PPAR) and sterol regulatory element-binding transcription protein 1 (SREBF1), which can regulate the transcription of several target genes (e.g., FASN, ACACA, SCD) involved in lipid metabolism have been extensively confirmed to play fundamental roles in the lipolytic or lipogenic state of several tissues in ruminants [7,8]. However, the extent of diet effects at the level of the digital cushion and consequently hoof health remains to be uncovered. Therefore, the objective of this study was to investigate the impact of feeding a higher-energy diet on both FA and transcriptomic profiles in the digital cushion of non-pregnant non-lactating dairy cows.

 

 

Materials and Methods

The Institutional Animal Care and Use Committee (IACUC) of the University of Illinois approved all procedures for this study (protocol #12134). Details of the experimental design have been published elsewhere [9]. Briefly, 14 non-lactating non-pregnant Holstein cows with initial BW = 717 ± 39 and initial BCS = 3.31 ± 0.14 were used. All cows were fed a control diet (low-energy, CON; NEL = 1.30 Mcal/kg) to meet 100% of National Research Council (NRC) requirements at ad libitum dry matter intake (DMI) for 3 weeks, after which half of the cows were assigned to a higher-energy diet (OVE; NEL = 1.60 Mcal/kg) and half of the cows continued on CON for 6 weeks. The OVE diet was fed ad libitum and resulted in cows consuming ~180% of NRC requirements, while CON cows were fed to consume only 100% of NRC. All cows were housed in ventilated indoor pens (10 m × 15 m; photoperiod of 8 hours light and 16 hours dark) with individual electronic transmission gates and transponders (American Calan, Northwood, NH) for access to feed. At the end of the experimental period cows were euthanized by captive bolt at the College of Veterinary Medicine diagnostic facilities (University of Illinois) after an overnight period without feed. Previous research has revealed that the architecture of the axial, middle and abaxial fat pads composing the digital cushion is different [10]. Because the middle fat pad was proposed to be the most-relevant in the context of ulcer development [10], it was chosen for the present study. After exsanguination, the lower right hind-limb was separated with a band saw, and a second cut was done in the lateral claw 2 cm above the coronary band in order to halve it longitudinally and expose the middle fat pad. Subsequently, a sample of tissue was harvested by blunt dissection and immediately frozen in liquid nitrogen.

Procedures for RNA extraction, cDNA synthesis, primer design and validation, and quantitative RT-PCR were exactly as described previously [9]. The quality of RNA samples was assessed using the 2100 Bioanalyzer (Agilent technologies Inc., Santa Clara, CA). The average RNA integrity number (RIN) of samples used was 7.5 ± 0.2. To address aspects of molecular regulation of adipogenesis, lipogenesis, and lipolysis we selected key genes (Table 1) associated with insulin signaling, carbohydrate metabolism, adipogenic and lipogenic transcription regulators, and regulation of lipolysis. Primer sequences are reported in the supplemental material. The normalization of gene expression data was performed using the geometric mean of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), beta-actin (ACTB) and ribosomal protein S9 (RPS9).

For determination of FA profile, twenty mg of sample were homogenized in 2 mL of 4:1 methanol and hexane (vol:vol) containing 30 μg of internal standard (TG:17 glyceryl triheptadecanoate) and 100 μg of butylated hydroxytoluene (BHT) solution. The homogenized samples were placed in glass tubes on ice under nitrogen for 20s. Subsequently, samples were placed in a water bath at 100°C and, after addition of 200 μL of acetyl chloride, incubated for 1 h. Samples were then cooled in an ice bath prior to addition of 5 mL K2CO3 buffer. Samples were vortexed for 1 min and then centrifuged at 2,000 × g at 4°C for 2 min. The upper phase containing FAME was transferred carefully to an auto-sampler glass vial (2 mL). The GC column used was a 15 m × 0.100 mm × 0.10 μm nitroterephthalic-acid-modified polyethylene glycol (PEG) column (DB_FFAP; cat No. 127-32H2; J and W scientific from Agilent Technology, USA). The temperature program included: initial 150°C with a 0.25 min hold; ramp: 35°C/min to 200°C, 8°C/min to 225°C with a 3.2 min hold, followed by 80°C/min to 248°C/min with 14.7 min hold. Carrier gas was H2 at a flow rate of 56.4 cm/s and a constant head pressure of 346.6 kPa; FID set at 250°C, air and nitrogen make-up gas flow rate of 400 mL/min and 30 mL/min, respectively, and H2 flow 40 mL/min. Split ratio was 200:1 with an auto sampler injection of 2 μL.

 

Statistical Analysis

After normalization with the geometric mean of the internal control genes, the real-time quantitative PCR data were log2 transformed before statistical analysis. The gene expression and FA data were analyzed using PROC MIXED of SAS (version 9.4; SAS Institute Inc., Cary, NC). The fixed effect in the model was diet (CON, OVE), and cow was designated as the random effect. Denominator degrees of freedom were computed by SAS with the statement DDFM = kr. Significant treatment effects were declared at P  0.05 and tendencies at P  0.15. For ease of interpretation the gene expression data are the log2-back transformed means that resulted from the statistical analysis.

 

 

Results

There was no diet effect (P 0.22) for most genes related to insulin signaling except for PDPK1 which was downregulated (P = 0.03) in OVE cows (Table 2). Except for a tendency (P  0.13) for greater expression of PPARG, CEBPA, and ADIPOQ in cows fed OVE, the expression of the adipogenic/lipogenic transcription regulators SREBF1 and RXRA was not affected (P 0.51). Despite the lack of effect on SREBF1, the expression of ACACA, FASN, SCD, and DGAT2 was upregulated (P  0.04) but ACSS2 downregulated (P = 0.01) with OVE (Table 2).

The expression of G6PD and IDHI, both important for generation of NADPH during lipogenesis, tended (P  0.07) to be greater with OVE (Table 2). However, the expression of LDHA, PCK1, and SLC2A4, which are associated with glucose metabolism and glyceroneogenesis, was not affected (P 0.21) by feeding OVE. Expression of the basal glucose transporter SLC2A1 tended (P = 0.08) to be upregulated with OVE (Table 2). Among genes encoding lipolytic proteins, the expression of the lipid droplet-associated protein PLIN2 was upregulated (P  0.05) but PLIN1 did not change (P = 0.70) in cows fed OVE. Although expression of GHR was upregulated (P = 0.05) by OVE, expression of ATGL, ABDH5, and LIPE only tended (P  0.11) to be upregulated (Table 2).

The concentration of MUFA of digital cushion tissue was not affected (P 0.16) by OVE (Table 3). However, eicosenoic acid (20:1n9) tended (P = 0.12) to be greater with OVE. Among the PUFA, eicosapentaenoic acid (20:5n3) was the only one affected by feeding OVE, which led to a lower (P = 0.04) concentration. Similar to 20:5n3, the concentration of dihomo-gammalinolenic acid (20:3n6), arachidonic acid (20:4n6), docosadienoic acid (22:2n6), docosapentaenoic acid (22:5n3), and docosahexaenoic acid (22:6n3) tended (P  0.15) to be lower with OVE (Table 3). In contrast to all the above PUFA, eicosatrienoic acid (20:3n3) was the only FA with a concentration that tended (P = 0.10) to increase with OVE. Among the SFA, arachidic acid (20:0) was the only one affected by OVE, which led to greater (P = 0.001) concentration (Table 3).


Discussion

During the transition period, dairy cows undergo several metabolic and physiologic adaptations in order to ensure a successful initiation of a new lactation cycle. Among these adaptations, the fat depots (e.g., subcutaneous, mesenteric) change from an adipogenic/lipogenic to a lipolytic state after parturition [11]. This effect is mainly attributed to a state of insulin resistance during the transition period [12]. It has been well-documented that feeding a higherenergy diet (primarily by increasing cereal grains) during the close-up period can induce alterations in the prepartal response of adipose to insulin and consequently alter lipid metabolism pathways, with a net result of enhancing body fat deposition [13,14]. In fact, these alterations on prepartal adipose tissue induced by higher-energy diets involve changes at the transcriptome level [5,15]. However, such transcriptomic adaptations have never been studied in the lipid-rich digital cushion of dairy cows.

Although the cows fed OVE in this study had lower plasma NEFA and greater insulin concentrations [9], this effect did not translate into an upregulation of INSR, IRS1, AKT1, or AKT2 all of which encode essential kinases related to insulin signaling. Such response is not surprising because the activity of these kinases is not controlled at the transcriptional level (Ji et al., 2012). The tendency for upregulation of the adipogenic transcription regulator PPARG and ADIPOQ with OVE does support enhanced insulin sensitivity just as it occurs in prepartal subcutaneous adipose tissue (Ji et al., 2012). Further evidence for enhanced insulin sensitivity in the digital cushion are the greater expression of G6PD, IDH1, and SLC2A1 also reported in prepartal subcutaneous adipose tissue of cows fed OVE [5].

The adipogenic/lipogenic role of PPARG, i.e. promoting maturation of pre-adipocytes, is attributed to the coordinated upregulation of several target genes involved in FA biosynthesis and adipogenesis [16]. The transcription factor SREBF1 plays a central role in the regulation of de novo FA synthesis in non-ruminants, particularly in the liver [17]. The lack of effect on SREBF1 with OVE resembles that of Ji et al. [5] and Hosseini et al. [9], where SREBF1 expression in subcutaneous adipose was not affected by feeding OVE. In contrast, similar to Moisa et al. [18] working with intramuscular fat of steers, the concomitant upregulation of ACACA, FASN, SCD, and DGAT2 along with PPARG due to feeding OVE indicate that insulin sensitivity in digital cushion can be enhanced by high-energy diets just as it occurs in subcutaneous fat. The fact that SREBF1 seems to play a central role during milk fat depression in dairy cows [19], along with the data from this and previous studies [20], indicates that this transcription regulator might be more important for the control of lipogenesis in the mammary gland instead of adipose tissue.

The results obtained on lipolytic genes in the current experiment were in agreement with those reported for subcutaneous adipose tissue by Ji et al. [5], where feeding a higher-energy diet during the close-up dry period resulted in transient or sustained upregulation of these genes. It is noteworthy that the expression of PLIN1, perilipin 1, was unresponsive to OVE in the present study just as reported previously in subcutaneous adipose tissue [5]. It could be possible that regulation of PLIN occurs at a post-transcriptional than transcriptional level [21]. In contrast, the tendency (P  0.11) for a concomitant upregulation of ATGL and ABDH5, both of which control basal lipolysis [21], with OVE indicated a predisposition towards lipolysis but agrees with data in prepartal subcutaneous adipose tissue in cows fed OVE [5]. Such effect has been reported following PPARγ activation in fully-differentiated adipocytes [22]

Regarding the control of lipolysis in the digital cushion during feeding of higher-energy diets prior to parturition, it is still unclear to what extent ATGL, ABDH5, and LIPE in digital cushion are sensitive to insulin signaling as is the case in subcutaneous adipose tissue [5,23]. A lack of change or an upregulation of ATGL and ABDH5 during the peripartal period in digital cushion would indicate a lipolytic state and, in fact, could serve to provide FA to the hoof/ corium tissue. Such mechanism seems biologically relevant because the hoof/corium requires FA for the synthesis of the lipid-rich extracellular matrix, the so-called intercellular cementing substance [24]. This is an essential element for final step in the keratinization process, where mature keratinocytes become glued together, and maintain hoof health [24].

The upregulation of GHR with OVE was consistent with previous findings in adipose tissue [25]. Thus, OVE could potentially increase responsiveness of the digital cushion to GH and, in turn, this effect might negatively affect insulin signaling as has been described for adipose tissue [26]. An increase in GH responsiveness could impact negatively overall lipid accumulation in the digital cushion of cows fed higher-energy diets. However, the fact that early lactation is characterized by higher circulating concentrations of GH and the mass of digital cushion also is highest at this time [5] casts some doubts on the anti-adipogenic role of GH at the level of digital cushion. Because the cows fed OVE in this study had lower plasma NEFA [9] it could be speculated that upregulation of ATGL, ABDH5, and LIPE in the digital cushion when circulating insulin is high reflects a process of re-cycling of FA rather than a lack of insulin sensitivity [21].

Regardless of diet, the concentration of MUFA and specifically oleic acid (18:1n9) was the highest among all FA detected, which is consistent with a previous report [4]. It is noteworthy that despite the upregulation of SCD in OVE-fed cows, this was not translated into a greater concentration of oleic acid. Therefore, it is possible that any alteration in diet composition with the aim to increase the energy density (i.e., OVE diet) might be partly responsible for this lack of effect. For instance, among the main alterations to the OVE diet from the CON diet was the inclusion of ~5% whole cottonseeds [9]. This oilseed has been associated with reduction in desaturase enzyme activity in adipose tissue of beef cattle [27]. In fact, cottonseeds contain significant amounts of sterculic acid [28], a type of cyclopropenoid FA, which is a well-established inhibitor of SCD activity in mouse [29]. The SCD gene was the most abundant gene (>76%; S1 File) in digital cushion regardless of dietary treatment. This is in line with the previously [4] observed greater concentration of MUFA in digital cushion in comparison with adipose tissue. The greater concentration of MUFA likely is one important feature of the shock-absorbing properties of digital cushion in the hoof. Therefore, the need for having greater amounts of SCD in this tissue is a priority in order to provide sufficient amounts of oleic acid

Among the FA measured in this study the concentration of arachidic acid (20:0) was the most-impacted by feeding OVE. In contrast to other 20-carbon unsaturated FA, e.g. arachidonic acid (20:4n6), arachidic acid has received less attention by the scientific community, primarily because 20:4n6 is mainly incorporated into cell membrane lipids (i.e., phospholipids) [30]. However, some have observed an upregulation of Ppara by 20:0 in liver of rats fed hyperglycemic diets [31]. If such an effect also occurs with bovine PPARG, then it could provide a partial explanation for the concomitant upregulation of PPARG and SCD. Because it is known that SCD can be upregulated by either PPARG or SREBF1 [8,32], based on the current results, it is reasonable to speculate that the upregulation of SCD was driven by PPARG. Regardless of the potential nutrigenomic effects of 20:0, it is evident that this FA in the digital cushion is responsive to dietary energy level. Further research on the biologic role of this FA within the context of lameness in dairy cows seems warranted

Alpha-linolenic acid (18:3n3) can be converted into the essential FA eicosapentaenoic acid (EPA; 20:5n3) and docosahexaenoic acid (DHA; 22:6n3) in mammalian tissues [33]. Although alpha-linolenic acid was not affected by OVE, the concentration of EPA and DHA (P = 0.06) was lower in OVE-fed cows. Interestingly, EPA, DHA, and arachidonic acid which tended to be lower (P = 0.12) with OVE, are precursors of eicosanoids, which in turn are important mediators of inflammation [34]. In fact, metabolites of EPA and DHA such as resolvins, protectins, and maresins are important during the resolution of inflammation [34].

Replacing corn gluten meal and blood meal with fish meal in diets fed to beef cattle as a source of PUFA can considerably increase the concentration of EPA and DHA in muscle [35]. In contrast, it is evident that increasing the energy density of OVE diet by adding ground corn and corn silage (8.5% and 20.9%, respectively), which are sources of oleic (18:1n9) and linoleic acid (18:2n6), in contrast to the CON diet [9], can decrease the concentration of EPA and DHA. Thus, composition of OVE compared with CON could partly explain the decrease in concentration of EPA and DHA in the digital cushion of OVE-fed cows. Taken together, we speculate that overfeeding cows with ground corn and corn silage-based diets could impair the local response and resolution of inflammatory conditions in the hoof. This is particularly important within the context of the periparturient period, where inflammatory stimuli are always present.

Overall, at the molecular and FA composition level, the digital cushion of dairy cows appears highly responsive to plane of dietary energy. Lipogenic genes were consistently upregulated by feeding the higher-energy diet, an effect partly orchestrated by PPARG rather than SREBF1. This is consistent with an extensive body of research performed on this transcription factor demonstrating that long-chain FA activate PPAR signaling. Arachidic acid was the most responsive FA to the OVE diet, indicating a potentially importance role for this FA in the biology of digital cushion. The decrease in concentration of anti-inflammatory FA (i.e., arachidonic acid, EPA, and DHA) in OVE-fed cows indicates that increasing diet energy density through greater inclusion of cereal grains might be detrimental for the mediation of inflammation in digital cushion. This negative effect could be further exacerbated by physiologic and endocrine changes during the peripartal period.

 

Supporting Information

S1 File. Table A. Features of primers used for qPCR analysis. Table B. qPCR performance. (DOCX)

 

Author Contributions

Conceived and designed the experiments: JJL JSO. Performed the experiments: ZMI HA EBRF AH. Wrote the paper: ZMI JSO JJL.

 

 

 

This article was originally published in PLoSONE11 (7): e0159536.doi:10.1371/journal.pone.0159536. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

 

 

 

References

1. Vermunt J (2007) One step closer to unravelling the pathophysiology of claw horn disruption: For the sake of the cows’ welfare. The Veterinary Journal 174: 219–220. PMID: 17141542

2. Greenough P, Vermunt J (1991) Evaluation of subclinical laminitis in a dairy herd and observations on associated nutritional and management factors. The veterinary record 128: 11–17. PMID: 1848379

3. Bicalho RC, Machado VS, Caixeta LS (2009) Lameness in dairy cattle: A debilitating disease or a disease of debilitated cattle? A cross-sectional study of lameness prevalence and thickness of the digital cushion. J Dairy Sci 92: 3175–3184. doi: 10.3168/jds.2008-1827 PMID: 19757545

4. Räber M, Scheeder MR, Ossent P, Lischer Ch J, Geyer H (2006) The content and composition of lipids in the digital cushion of the bovine claw with respect to age and location—a preliminary report. Vet J 172: 173–177. PMID: 16772143

5. Ji P, Osorio J, Drackley J, Loor J (2012) Overfeeding a moderate energy diet prepartum does not impair bovine subcutaneous adipose tissue insulin signal transduction and induces marked changes in peripartal gene network expression. Journal of Dairy Science 95: 4333–4351. doi: 10.3168/jds.2011-5079 PMID: 22818447

6. Weber M, Locher L, Huber K, Kenéz Á, Rehage J, Tienken R et al. (2015) Longitudinal changes in adipose tissue of dairy cows from late pregnancy to lactation. Part 1: The adipokines apelin and resistin and their relationship to receptors linked with lipolysis. Journal of dairy science 99: 1549–1559. doi: 10. 3168/jds.2015-10131 PMID: 26686707

7. Harvatine K, Boisclair Y, Bauman D (2009) Recent advances in the regulation of milk fat synthesis. Animal 3: 40–54. doi: 10.1017/S1751731108003133 PMID: 22444171

8. Bionaz M, Chen S, Khan MJ, Loor JJ (2013) Functional role of PPARs in ruminants: Potential targets for fine-tuning metabolism during growth and lactation. PPAR Res 2013: 684159. doi: 10.1155/2013/ 684159 PMID: 23737762

9. Hosseini A, Tariq MR, Trindade da Rosa F, Kesser J, Iqbal Z, Mora O et al. (2015) Insulin Sensitivity in Adipose and Skeletal Muscle Tissue of Dairy Cows in Response to Dietary Energy Level and 2,4-Thiazolidinedione (TZD). PLoS One 10: e0142633. doi: 10.1371/journal.pone.0142633 PMID: 26571137

10. Raber M, Lischer Ch J, Geyer H, Ossent P (2004) The bovine digital cushion—a descriptive anatomical study. Vet J 167: 258–264. PMID: 15080874

11. McNamara JP, Harrison JH, Kincaid RL, Waltner SS (1995) Lipid metabolism in adipose tissue of cows fed high fat diets during lactation. J Dairy Sci 78: 2782–2796. PMID: 8675761

12. Bauman D, Currie W (1980) Partitioning of nutrients during pregnancy and lactation: a review of mechanisms involving homeostasis and homeorhesis. Journal of dairy science 63: 1514–1529. PMID: 7000867

13. Dann H, Litherland N, Underwood J, Bionaz M, D’angelo A, McFadden JW et al. (2006) Diets during far-off and close-up dry periods affect periparturient metabolism and lactation in multiparous cows. Journal of dairy science 89: 3563–3577. PMID: 16899692

14. Janovick NA, Boisclair YR, Drackley JK (2011) Prepartum dietary energy intake affects metabolism and health during the periparturient period in primiparous and multiparous Holstein cows. Journal of dairy science 94: 1385–1400. doi: 10.3168/jds.2010-3303 PMID: 21338804

15. Vailati-Riboni M, Kanwal M, Bulgari O, Meier S, Priest N, Burke CR et al. (2016) Body condition score and plane of nutrition prepartum affect adipose tissue transcriptome regulators of metabolism and inflammation in grazing dairy cows during the transition period. Journal of dairy science 99: 758–770. doi: 10.3168/jds.2015-10046 PMID: 26601585

16. Kadegowda A, Bionaz M, Piperova L, Erdman R, Loor J (2009) Peroxisome proliferator-activated receptor-γ activation and long-chain fatty acids alter lipogenic gene networks in bovine mammary epithelial cells to various extents. Journal of Dairy Science 92: 4276–4289. doi: 10.3168/jds.2008-1932 PMID: 19700688

17. Desvergne B, Michalik L, Wahli W (2006) Transcriptional regulation of metabolism. Physiological reviews 86: 465–514. PMID: 16601267

18. Moisa SJ, Shike DW, Meteer WT, Keisler D, Faulkner DB, Loor J (2013) Yin yang 1 and adipogenic gene network expression in longissimus muscle of beef cattle in response to nutritional management. Gene Regul Syst Bio 7: 71–83. doi: 10.4137/GRSB.S11783 PMID: 23700364

19. Bauman D, Griinari J (2003) Nutritional regulation of milk fat synthesis. Annual review of nutrition 23: 203–227. PMID: 12626693

20. Thering B, Graugnard D, Piantoni P, Loor J (2009) Alterations in adipose tissue lipogenic gene networks due to lipid feeding and milk fat depression in lactating cows. Journal of Dairy Science: 4290– 4300.

21. Duncan R, Ahmadian M, Jaworski K, Sarkadi-Nagy E, Sul H (2007) Regulation of lipolysis in adipocytes. Annual review of nutrition 27: 79. PMID: 17313320

22. Kershaw E, Schupp M, Guan H, Gardner N, Lazar M, Flier JS (2007) PPARγ regulates adipose triglyceride lipase in adipocytes in vitro and in vivo. American Journal of Physiology-Endocrinology and Metabolism 293: E1736–E1745. PMID: 17848638

23. Koltes D, Spurlock D (2011) Coordination of lipid droplet-associated proteins during the transition period of Holstein dairy cows. Journal of dairy science 94: 1839–1848. doi: 10.3168/jds.2010-3769 PMID: 21426973

24. Tomlinson D, Mülling C, Fakler T (2004) Invited review: formation of keratins in the bovine claw: roles of hormones, minerals, and vitamins in functional claw integrity. Journal of dairy science 87: 797–809. PMID: 15259213

25. Rhoads RP, Kim JW, Van Amburgh ME, Ehrhardt RA, Frank SJ, Boisclair YR (2007) Effect of nutrition on the GH responsiveness of liver and adipose tissue in dairy cows. J Endocrinol 195: 49–58. PMID: 17911396

26. del Rincon JP, Iida K, Gaylinn BD, McCurdy CE, Leitner JW, Barbour LA (2007) Growth hormone regulation of p85alpha expression and phosphoinositide 3-kinase activity in adipose tissue: mechanism for growth hormone-mediated insulin resistance. Diabetes 56: 1638–1646. PMID: 17363744

27. Yang A, Larsen TW, Smith SB, Tume RK (1999) Delta9 desaturase activity in bovine subcutaneous adipose tissue of different fatty acid composition. Lipids 34: 971–978. PMID: 10574662

28. Obert JC, Hughes D, Sorenson WR, McCann M, Ridley WP (2007) A quantitative method for the determination of cyclopropenoid fatty acids in cottonseed, cottonseed meal, and cottonseed oil (Gossypium hirsutum) by high-performance liquid chromatography. J Agric Food Chem 55: 2062–2067. PMID: 17323967

29. Ortinau LC, Pickering RT, Nickelson KJ, Stromsdorfer KL, Naik CY, Haynes RA (2012) Sterculic Oil, a Natural SCD1 Inhibitor, Improves Glucose Tolerance in Obese ob/ob Mice. ISRN Endocrinol 2012: 947323. doi: 10.5402/2012/947323 PMID: 23209931

30. Leslie CC (1997) Properties and regulation of cytosolic phospholipase A2. The Journal of biological chemistry 272: 16709–16712. PMID: 9201969

31. Moises Laparra J, Diez-Municio M, Javier Moreno F, Herrero M (2015) Kojibiose ameliorates arachidic acid-induced metabolic alterations in hyperglycaemic rats. Br J Nutr 114: 1395–1402. doi: 10.1017/ S0007114515003153 PMID: 26344377

32. Ma L, Corl BA (2012) Transcriptional regulation of lipid synthesis in bovine mammary epithelial cells by sterol regulatory element binding protein-1. J Dairy Sci 95: 3743–3755. doi: 10.3168/jds.2011-5083 PMID: 22720931

33. Yang G, Bu DP, Wang JQ, Khas E, Zhou LY, Loor J (2012) Duodenal infusion of alpha-linolenic acid affects fatty acid metabolism in the mammary gland of lactating dairy cows. J Dairy Sci 95: 5821–5830. doi: 10.3168/jds.2011-4893 PMID: 22921622

34. Szefel J, Kruszewski WJ, Sobczak E (2015) Factors influencing the eicosanoids synthesis in vivo. Biomed Res Int 2015: 690692. doi: 10.1155/2015/690692 PMID: 25861641

35. Mandell IB, Buchanan-Smith JG, Holub BJ, Campbell CP (1997) Effects of fish meal in beef cattle diets on growth performance, carcass characteristics, and fatty acid composition of longissimus muscle. J Anim Sci 75: 910–919. PMID: 9110201

 
Author/s
Dr. Loor´s Research Interests are Systems biology; molecular nutrition; genomics; metabolomics; bioinformatics; nutritional programming of adipose tissue; mammary gland development; lipid metabolism; conjugated linoleic acids (CLA); nutritional and physiological genomics; comparative genomics; regulation of milk fat and protein synthesis; nutritional regulation of muscle development. His research program focuses on the study of how nutrition, physiological state and their interaction affect tissue function and metabolic adaptations through alterations in the transcriptome...
 
remove_red_eye 575 forum 1 bar_chart Statistics share print
Share :
close
See all comments
 
   | 
Copyright © 1999-2020 Engormix - All Rights Reserved