Abstract:One of the most controversial aspects of the use of animals in science is the production of pain. Pain is a central ethical concern. The activation of neural pathways involved in the pain response has physiological, endocrine, and behavioral consequences, that can affect both the health and welfare of the animals, as well as the validity of research. The strategy to prevent these consequences requires understanding of the nociception process, pain itself, and how assessment can be performed using validated, no… Show more
“…However, a possible explanation for why nociception/pain might be present could be due to the activation of peripheral nociceptors located in the skin and muscles of the cervical region of rodents and to the potential sensitization of nociceptors due to negative states derived from decapitation (e.g., fear). Although the loss of consciousness is fast after decapitation, before head detachment, tissular damage to said structures would trigger the nociceptive pathway (e.g., transduction, transmission, modulation, projection, and perception) culminating in pain perception for a couple of seconds before the cessation of nervous signaling [7,21,62]. It is known that after decapitation there is an anatomical disconnection between the mesencephalon and the cardiorespiratory centers-leading to death-and that the electric signaling present postdecapitation cannot solely be attributed to nociception since it has been found in healthy anesthetized animals or during REM sleep [14,33].…”
Section: Discussionmentioning
confidence: 99%
“…Currently, studying pain facial expressions in domestic and wildlife species is a trend derived from Darwin's studies regarding emotion and its association with facial expressions [19]. This has led to the development of "grimace scales", scoring systems that categorize movements of facial muscles-called Facial Action Units (FAUs)-related to pain [20][21][22][23]. For rats, Sotocinal et al [22] developed the Rat Grimace Scale (RGS), using as a basis the Mouse Grimace Scale (MGS), a validated tool that uses four FAUs to determine the pain level: 1. ear change; 2. orbital tightening; 3. nose/cheek flattening; and 4. whisker change.…”
Refinement of experimental procedures in animal research has the objective of preventing and minimizing pain/distress in animals, including the euthanasia period. This study aimed to evaluate pain associated with six methods of euthanasia in Wistar rats (injectable, inhalational, and physical), by applying the Rat Grimace Scale (RGS), comparing the scores, and determining the method with the highest score that might indicate pain for laboratory rodents. Sixty adult male and female Wistar rats were used and assigned to six treatments: pentobarbital, CO2, decapitation, isoflurane, ketamine + xylazine, and ketamine + CO2. Video recording to assess the RGS scores was performed in four events: basal: 24 h before the procedure; Ti1: three minutes before the procedure; Ti2: during the application of the euthanasia method; and Ti3: immediately after the application until LORR. The main findings of this study showed that, during Ti2, decapitation and ketamine + xylazine had the highest scores (0.6 ± 0.26 and 0.6 ± 0.16, respectively) (p < 0.0001), while at Ti3, CO2 (0.9 ± 0.18) and isoflurane (1.2 ± 0.20) recorded the highest scores (p < 0.0001). According to the present results, decapitation and ketamine + xylazine elicited short-term acute pain, possibly due to tissue damage caused by both methods (injection and guillotine). In contrast, isoflurane’s RGS scores recorded during Ti3 might be associated with nociception/pain due to the pungency of the drug or to the pharmacological muscle relaxant effect of isoflurane. Further research is needed to establish a comprehensive study of pain during euthanasia, where RGS could be used minding the limitations that anesthetics might have on facial expression.
“…However, a possible explanation for why nociception/pain might be present could be due to the activation of peripheral nociceptors located in the skin and muscles of the cervical region of rodents and to the potential sensitization of nociceptors due to negative states derived from decapitation (e.g., fear). Although the loss of consciousness is fast after decapitation, before head detachment, tissular damage to said structures would trigger the nociceptive pathway (e.g., transduction, transmission, modulation, projection, and perception) culminating in pain perception for a couple of seconds before the cessation of nervous signaling [7,21,62]. It is known that after decapitation there is an anatomical disconnection between the mesencephalon and the cardiorespiratory centers-leading to death-and that the electric signaling present postdecapitation cannot solely be attributed to nociception since it has been found in healthy anesthetized animals or during REM sleep [14,33].…”
Section: Discussionmentioning
confidence: 99%
“…Currently, studying pain facial expressions in domestic and wildlife species is a trend derived from Darwin's studies regarding emotion and its association with facial expressions [19]. This has led to the development of "grimace scales", scoring systems that categorize movements of facial muscles-called Facial Action Units (FAUs)-related to pain [20][21][22][23]. For rats, Sotocinal et al [22] developed the Rat Grimace Scale (RGS), using as a basis the Mouse Grimace Scale (MGS), a validated tool that uses four FAUs to determine the pain level: 1. ear change; 2. orbital tightening; 3. nose/cheek flattening; and 4. whisker change.…”
Refinement of experimental procedures in animal research has the objective of preventing and minimizing pain/distress in animals, including the euthanasia period. This study aimed to evaluate pain associated with six methods of euthanasia in Wistar rats (injectable, inhalational, and physical), by applying the Rat Grimace Scale (RGS), comparing the scores, and determining the method with the highest score that might indicate pain for laboratory rodents. Sixty adult male and female Wistar rats were used and assigned to six treatments: pentobarbital, CO2, decapitation, isoflurane, ketamine + xylazine, and ketamine + CO2. Video recording to assess the RGS scores was performed in four events: basal: 24 h before the procedure; Ti1: three minutes before the procedure; Ti2: during the application of the euthanasia method; and Ti3: immediately after the application until LORR. The main findings of this study showed that, during Ti2, decapitation and ketamine + xylazine had the highest scores (0.6 ± 0.26 and 0.6 ± 0.16, respectively) (p < 0.0001), while at Ti3, CO2 (0.9 ± 0.18) and isoflurane (1.2 ± 0.20) recorded the highest scores (p < 0.0001). According to the present results, decapitation and ketamine + xylazine elicited short-term acute pain, possibly due to tissue damage caused by both methods (injection and guillotine). In contrast, isoflurane’s RGS scores recorded during Ti3 might be associated with nociception/pain due to the pungency of the drug or to the pharmacological muscle relaxant effect of isoflurane. Further research is needed to establish a comprehensive study of pain during euthanasia, where RGS could be used minding the limitations that anesthetics might have on facial expression.
“…Oxidative stress can damage DNA, leading to mutations and potentially harmful consequences. Microalgae-derived antioxidants may aid in DNA repair mechanisms, preventing long-term damage and maintaining genetic integrity [70].…”
Section: Mechanisms Of Action Of Microalgae-derived Antioxidantsmentioning
In recent times, there has been a revolutionary surge in antioxidant research, with a focus on harnessing microalgae to enhance wellness and extend human longevity. Microalgae, a diverse group of unicellular photosynthetic organisms, have emerged as promising sources of natural antioxidants due to their ability to synthesize various bioactive compounds, including carotenoids, polyphenols, and tocopherols. These antioxidants play a pivotal role in scavenging free radicals and reducing oxidative stress, known contributors to aging and chronic diseases. This review provides an over-view of recent advancements in understanding microalgae’s antioxidant potential, covering their biochemical composition, extraction techniques, and purification methods. Moreover, it delves into compelling in vitro and in vivo studies showcasing microalgae-derived antioxidants’ protective effects against oxidative damage, inflammation, cardiovascular diseases, and neurodegenerative disorders. The sustainable cultivation of microalgae in controlled environments further supports the potential for large-scale production and commercialization of their antioxidant compounds. As microalgae continue to revolutionize antioxidant research, they hold immense promise in developing novel preventive and therapeutic strategies to promote human health and wellbeing.
“…An important field of research where IRT could help to refine and promote animal welfare is during the slaughter or euthanasia of farm, companion, and laboratory animals in order to prevent pain and negative emotional states [ 74 , 139 , 140 ]. Weschenfelder et al [ 74 ] have used infrared ocular thermography in pigs during slaughter to associate the physiological response with meat quality.…”
Section: Future Research On Irt Applicationmentioning
Pain assessment in domestic animals has gained importance in recent years due to the recognition of the physiological, behavioral, and endocrine consequences of acute pain on animal production, welfare, and animal model validity. Current approaches to identifying acute pain mainly rely on behavioral-based scales, quantifying pain-related biomarkers, and the use of devices monitoring sympathetic activity. Infrared thermography is an alternative that could be used to correlate the changes in the superficial temperature with other tools and thus be an additional or alternate acute pain assessment marker. Moreover, its non-invasiveness and the objective nature of its readout make it potentially very valuable. However, at the current time, it is not in widespread use as an assessment strategy. The present review discusses scientific evidence for infrared thermography as a tool to evaluate pain, limiting its use to monitor acute pain in pathological processes and invasive procedures, as well as its use for perioperative monitoring in domestic animals.
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