Differential Transcription of Selected Cytokine and Neuroactive Ligand-receptor Genes in Peripheral Leukocytes from Calves in Response to Cautery Disbudding.
Kavitha KongaraVenkata Sayoji Rao DukkipatiHui Min TaiAxel HeiserAlan MurrayJames WebsterCraig Brian JohnsonPublished in: Animals : an open access journal from MDPI (2020)
Calf disbudding is a painful husbandry practice on dairy and beef cattle farms. An objective measurement of pain is useful to reliably evaluate the pain intensity and anti-nociceptive (analgesic) efficacy of therapeutic agents. The aim of this study was to investigate the changes in peripheral leucocyte inflammatory cytokine gene expression in calves after disbudding, and to assess whether the changes in cytokine gene expression could be an indicator of the efficacy of analgesic drugs. In a randomised controlled study, 16 calves (aged 31 to 41 days and weighing 58 to 73 kg), undergoing routine disbudding, were randomly allocated into two groups (n = 8 in each group). Calves in the control group received no analgesic, while those in the treatment group received 0.5 mg kg-1 meloxicam subcutaneously prior to disbudding. Disbudding was performed using an electric debudder. Blood (10 mL) was sampled from the jugular vein just before and 4 and 24 h post-disbudding, RNA was extracted from leukocytes, and the transcription of 12 genes of interest was assessed using nCounter gene expression assay. The results showed significantly higher transcription (compared to baseline values) of the studied genes (except CRH, IFNγ, and IL10) in the control group calves at either 4 or 24 h post-disbudding. The administration of meloxicam one hour before disbudding significantly attenuated the upregulation of IL6, PGHS2, TAC1, NOS1, and CRH gene transcription post-disbudding, while it did not suppress the elevated transcription of acute and pro-inflammatory cytokines such as IL1β, IFNγ, IL8, and TNFα genes. In conclusion, nCounter gene expression assay seems to be a promising tool to study the expression of cytokine genes and thus could be used for the pre-clinical evaluation of novel analgesics.
Keyphrases
- gene expression
- genome wide
- dna methylation
- neuropathic pain
- genome wide identification
- transcription factor
- chronic pain
- bioinformatics analysis
- poor prognosis
- anti inflammatory
- healthcare
- primary care
- high throughput
- immune response
- blood pressure
- clinical trial
- dendritic cells
- pain management
- open label
- spinal cord
- cell proliferation
- spinal cord injury
- drug induced
- intensive care unit
- extracorporeal membrane oxygenation
- signaling pathway
- ultrasound guided
- smoking cessation
- aortic dissection