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Nanoencapsulated Melaleuca alternifolia essential oil exerts anesthetic effects in the brachyuran crab using Neohelice granulate

ABSTRACT

The aim of this study was to evaluate the efficacy and safety of several anesthetics in the brachyuran crab Neohelice granulata, an emergent experimental model. The essential oils (EOs) of Lippia alba, Aloysia tryphilla, and Melaleuca alternifolia (tea tree oil; TTO), the isolated compounds eugenol, menthol, terpinen-4-ol, and the nanoencapsulated form of TTO, were administered in one or more of the following ways: added to the water (immersion), through an arthrodial membrane (injected), or by oral gavage. Unexpectedly, most EOs did not produce an anesthetic effect after immersion. Only TTO and eugenol induced anesthesia by immersion, with very long induction and recovery times compared to anesthesia of other crustaceans. However, a good anesthetic effect was observed with the injection of terpinen-4-ol and nanoencapsulated TTO in N. granulata; both demonstrated ideal induction and recovery times. These substances appear to be promising anesthetic alternatives for crustaceans.

Key words:
anesthesia; eugenol; terpinen-4-ol; nanotechnology; invertebrate; tea-tree-oil

INTRODUCTION

Crustaceans may experience pain and stress in ways that are analogous to those of vertebrates, demonstrating a similar experience in terms of suffering (Elwood and Appel 2009ELWOOD RW AND APPEL M. 2009. Pain experience in hermit crabs? Anim Behav 77: 1243-1246.). In this sense, using different noxious stimuli and behavioral responses to indicate pain, study conducted by Barr et al. (2008BARR S, LAMING PR, DICK JTA AND ELWOOD RW. 2008. Nociception or pain in a decapod crustacean? ‎Anim Behav 75: 745-751.) demonstrated that crustacean Palaemon elegans presents a physiological stress response analogous to the pain observed in vertebrates, concluding that this specie needs attention during manipulation.

Current methods for stunning, anesthesia, and euthanasia include freezing, direct blunt force in the rostrum, injection of magnesium chloride or potassium chloride, or carbon dioxide (CO2) exposure (Cooper 2011COOPER JE. 2011. Anesthesia, analgesia, and euthanasia of invertebrates. ILAR J 52: 196-204.). However, these methods are not considered safe or suiTable In accordance with the American Veterinary Medical Association (AVMA 2007); thus, alternative methods, such as the use of anesthetics, are required to avoid or minimize the suffering of animals. Moreover, recently it has been shown that the crustacean nervous system is capable of preserving nerve cell communication and rhythmicity even at extremely low temperatures (Marder et al. 2011MARDER E. 2011. Variability, compensation, and modulation in neurons and circuits. Proc Natl Acad Sci USA 108: 15542-15548., Tang et al. 2012TANG LS, TAYLOR AL, RINBERG A AND MARDER E. 2012. Robustness of a rhythmic circuit to short- and long-term temperature changes. J Neurosci 32: 10075-10085.). Magnesium chloride and exposure to CO2 are not effective as anesthetics, and CO2 reduces water pH, leading to stress before paralysis and/or death (Fregin and Bickmeyer 2016FREGIN T AND BICKMEYER U. 2016. Electrophysiological investigation of different methods of anesthesia in lobster and crayfish. PLoS ONE 11: e0162894.). This has led us to question how decapod crustaceans can be safely anesthetized before treating them in physiological experiments or carcinoculture.

In fish farming, anesthetics have been successfully used to minimize stress and pain, facilitate handling and transport, and prevent injury (Gunkel et al. 2007GUNKEL CI AND LEWBART GA. 2007. Invertebrates. In: West GD, Heard DJ and Caulkett NA (Eds), Zoo & Wildlife Immobilization and Anesthesia, Blackwell Publishing, Ames, Iowa, p. 147-158., Ross and Ross 2008ROSS LG AND ROSS B. 2008. Anaesthetic and sedative techniques for aquatic animals. 3rd ed., Oxford, Blackwell, p. 236. ). Crustaceans can also be anesthetized with synthetic anesthetics, such as tricaine methanesulfonate (MS-222), isobutyl alcohol, and intramuscular injections of lidocaine, ketamine, pentobarbital, propofol, tiletamine-zolazepam, or xylazine (Brown et al. 1996BROWN PB, WHITE MR, CHAILLE J, RUSSELL M AND OSETO C. 1996. Evaluation of three anesthetic agents for crayfish (Orconectes virilis). J Shellfish Res 15: 433-435., Ferraro and Pressacco 1996FERRARO EA AND PRESSACCO L. 1996. Anesthetic procedures for crustaceans. An assessment of isobutanol and xylazine as general anaesthetics for Squilla mantis (Stomapoda). Mem Biol Mar Oceanogr 12: 471-475., Quesada et al. 2011QUESADA RJ, SMITH CD AND HEARD DJ. 2011. Evaluation of parenteral drugs for anesthesia in the blue crab (Callinectes sapidus). J Zoo Wildl Med 42: 295-299.). However, the use of synthetic anesthetics can be harmful to animals. For example, MS-222 can be toxic and may cause aversive reactions (Yue 2008YUE S. 2008. The welfare of crustaceans at slaughter, Humane Society of the United States 1, 10 p.).

Alternatively, the use of natural products with anesthetic potential, such as clove oil (Eugenia aromatica essential oil), have shown promise, and may offer more security for animals (Morgan et al. 2001MORGAN J, CARGILL C AND GROOT E. 2001. The efficacy of clove oil as an anesthetic for decapod crustaceans. Bull Aquacult Assoc Can 101: 27-31.). Several studies have demonstrated that clove oil is a popular anesthetic for procedures such as handling and transportation of some aquatic animals (Keene et al. 1998KEENE JL, NOAKES DLG, MOCCIA RD AND SOTO CG. 1998. The efficacy of clove oil as an anaesthetic for rainbow trout, Oncorhynchus mykiss (Walbaum). Aquacult Res 29: 89-101., Griffiths 2000GRIFFITHS SP. 2000. The use of clove oil as an anaesthetic and method for sampling intertidal rockpool fishes. J Fish Biol 57: 1453-64.). In addition, clove oil has already been tested for cephalopods (Seol et al. 2007SEOL DW, LEE J, IM SY AND PARK IS. 2007. Clove oil as an anaesthetic for common octopus (Octopus minor, Sasaki). Aquacult Res 38: 45-49. , Gonçalves et al. 2012GONÇALVES RA, ARAGÃO C, FRIAS PA AND SYKES AV. 2012. The use of different anaesthetics as welfare promoters during short-term human manipulation of European cuttlefish (Sepia officinalis) juveniles. Aquaculture 370/371: 130-135.), amphibians (Hernández et al. 2012HERNÁNDEZ SE, SERNIA C AND BRAD AJ. 2012. The effect of three anaesthetic protocols on the stress response in cane toads (Rhinella marina). Vet Anaesth Analg 239: 584-590.), and crustaceans (Keene et al. 1998, Morgan et al. 2001, Bownik 2015BOWNIK A. 2015. Clove essential oil from Eugenia caryophyllus induces anesthesia, alters swimming performance, heart functioning and decreases survival rate during recovery of Daphnia magna. Turk J Fish Aquat Sci 15: 157-166., Premarathna et al. 2016PREMARATHNA AD, PATHIRANA I, JAYANTHA RAJAPAKSE RPV AND PATHIRANA E. 2016. Evaluation of efficacy of selected anesthetic agents on blood-spotted crab (Portunus sanguinolentus). J Shellfish Res 35: 237-240.). Eugenol, the major compound of clove oil, and the essential oils (EOs) of Lippia alba and Aloysia triphylla are effective anesthetics for white shrimp (Litopenaeus vannamei) and can be used for short-term anesthesia and transport (Parodi et al. 2012PARODI TV ET AL. 2012. The anesthetic efficacy of eugenol and the essential oils of Lippia alba and Aloysia triphylla in post-larvae and subadults of Litopenaeus vannamei (Crustacea, Penaeidae). Comp Biochem Physiol C 155: 462-468.). However, anesthesia studies in brachyuran decapods are still scarce.

Based on the evidences, our hypothesis is that use of essential oils can be a new approach to anesthesia of invertebrates in order to reduce or avoid the physiological stress during manipulation or invasive procedures. Thus, the aim of this study was to investigate the anesthetic efficiency of different natural products using the brachyuran crab, Neohelice granulata, as an experimental model.

MATERIALS AND METHODS

ANIMALS

Adult male N. granulata crabs (n = 250) (10.2 ± 0.35 g) were collected in salt marshes around Rio Grande city, Southern Brazil, and transported to a laboratory. The animals were acclimated for at least 15 days before the experiments. Individuals were kept in tanks, with free access to air at 20°C, 20 ppm of salinity, 12L:12D photoperiod, and 6.5 mg O2. L-1. The crabs were fed ad libitum with ground beef three times a week until the day of the experiment.

Essential oil of the leaves of Melaleuca alternifolia (tea tree oil; TTO) was purchased from Química Delaware Ltda, Brazil, and eugenol (99% purity) was purchased from Biodinâmica™, Ibiporá, PR, Brazil. Nanoencapsulated TTO was obtained from Inventiva® (Porto Alegre, Brazil), and terpinen-4-ol was obtained from Sigma-Aldrich Corporation (St. Louis, United States, purity ≥97%). Menthol (99.5% purity) was purchased from Vetec® (Rio de Janeiro, Brazil). Essential oils of Lippia alba (EOLA) and Aloysia triphylla (EOAT) were obtained from fresh plants cultivated at the campus of the Universidade Federal de Santa Maria, in the city of Frederico Westphalen, Southern Brazil. The oil extraction from the leaves of these plants was performed by steam distillation, in a Clevenger apparatus and stored at -20oC until use. EOLA, EOAT, and TTO composition was analyzed by gas chromatography. It is important emphasize that A. triphylla and L. alba showed potent anesthetic effects for withe shrimp (L. vannamei), as demonstrated by Parodi et al. (2012PARODI TV ET AL. 2012. The anesthetic efficacy of eugenol and the essential oils of Lippia alba and Aloysia triphylla in post-larvae and subadults of Litopenaeus vannamei (Crustacea, Penaeidae). Comp Biochem Physiol C 155: 462-468.), while the M. alternifolia essential oil and terpinen-4-ol demonstrated potential anesthetic effects to silver catfish (Rhamdia quelen) (Souza et al. 2018SOUZA CF, BALDISSERA MD, SILVA LL, GEIHS M AND BALDISSEROTTO B. 2018. Is monoterpene terpinen-4-ol the compound responsible for the anesthetic and antioxidant activity of Melaleuca alternifolia essential oil (tea tree oil) in silver catfish? Aquaculture 486: 217-223.), which aroused our interest in the use of these essential oils as possible anesthetic to N. granulata.

Gas chromatography-mass spectrometry total ion chromatogram analysis was performed using an Agilent-6890 gas chromatograph coupled with an Agilent 5973 mass selective detector under the following conditions: HP-5MS column, 5%-phenyl-95%-methylsiloxane, 30 m × 0.25 mm × 0.25 µm; EI-MS, 70 eV; operating conditions, split inlet 1:100, temperature program 40-260°C, 40°C for 4 min, ramp rate 4°C/min, carrier gas He, flow rate 1 mL min−1, injector and detector temperature 220°C, interface temperature 250°C, Databank (NIST 2002).

The constituents of the EOs were identified by comparing their mass spectra with a mass spectral library (NIST 2002) and by comparison of the Kovats retention index with data in the literature (Adams 2001ADAMS RP. 2001. Identification of Essential Oil Components by Gas Chromatography/ Quadruple Mass Spectroscopy. Allured Publishing Corporation, Illinois, 455 p.).

The principal compounds in EOAT were E-citral (42.30%) and Z-citral (29.92%), while linalool (55.25%) was the most abundant compound for EOLA, and for TTO the majorities components were terpinen-4-ol (41.98%), γ-terpinene (20.15%), and α-terpinene (9.85%) (Parodi et al. 2012PARODI TV ET AL. 2012. The anesthetic efficacy of eugenol and the essential oils of Lippia alba and Aloysia triphylla in post-larvae and subadults of Litopenaeus vannamei (Crustacea, Penaeidae). Comp Biochem Physiol C 155: 462-468., Saccol et al. 2013SACCOL EMH ET AL. 2013. Addition of Lippia alba (Mill) N.E. Brown essential oil to the diet of the silver catfish: analysis of growth, metabolic and blood parameters and the antioxidant response. Aquaculture 416/417: 244-254., Baldissera et al. 2016BALDISSERA MD, GRANDO TH, SOUZA CF, GRESSLER LT, STEFANI LM, SILVA AS AND MONTEIRO SG. 2016. In vitro and in vivo action of terpinen-4-ol, γ-terpinene, and α-terpinene against Trypanosoma evansi. Exp Parasitol 162: 43-48.).

PREPARATION OF ANESTHETICS

For immersion tests, EOs, eugenol, and menthol were previously dissolved in ethanol at a ratio of 1:10 (stock solution) before they were added to the water. For injection or gavage tests, eugenol and menthol were used after being dissolved in ethanol or diluted in physiological solution for crustaceans (Maciel et al. 2014MACIEL FE, GEIHS MA, CRUZ BP, VARGAS MA, ALLODI S, MARINS LF AND NERY LEM. 2014. Melatonin as a signaling molecule for metabolism regulation in response to hypoxia in the crab Neohelice granulata. Int J Mol Sci 15: 22405-22420.). Terpinen-4-ol and nanoencapsulated TTO were used pure or diluted in physiological solution.

ANESTHETIC TESTS

Crabs were selected randomly for each experimental group (n = 5), and each animal was used only once. We divided the anesthetic tests into two experiments. In the first experiment, EOs and natural compounds were tested. In the second experiment, as TTO was the only EO with an anesthetic effect (see results), we decided to investigate the use of the major isolated compound derived from TTO.

EXPERIMENT 1

For the immersion tests, crabs were transferred to aquaria containing 1 L of continuously aerated sea water (20 ppm) together with 300, 500, 1000, 2000, 3000, 5000, or 8000 µL L-1 of eugenol, EOLA, EOAT, and TTO, or 1500, 4000, and 10000 µL L-1 of menthol. Exposure to ethanol was also performed at the same concentration used for dilution of the highest EO concentrations.

Insulin syringes (BD Ultra-Fine ™) were used for the injection tests with 25 or 50 µL of EOs, eugenol, and menthol. Subsequently, these products were also tested diluted 10, 100, 1000, 10000, or 100000-fold in crustacean physiological solution. The needle was inserted through the arthrodial membrane between the carapace and the coxa of the swimming pereopod. Insulin syringes were inserted in the oral cavity for the gavage with 50 µL of EOs (Figure 1).

Figure 1
Sites of injection (arrows) used in this study.

The behavior of the crabs was observed to evaluate the time required for the induction of anesthesia, based on the procedure reported by Gardner (1997GARDNER C. 1997. Options for humanely immobilizing and killing crabs. J Shellfish Res 16: 219-224.) and Morgan et al. (2011), with some adaptations (Table I). Crabs were classified as in the stage of sedation when they demonstrated partial loss of equilibrium, but were still reactive to touch stimuli. Crabs were classified as in the stage of anesthesia when they demonstrated complete loss of equilibrium and were not reactive to stimuli. After induction, the crabs were transferred to an anesthetic-free aquarium to measure the anesthesia recovery time. Animals were considered recovered when normal equilibrium and reaction to external stimuli were observed.

TABLE I
Evaluation of anesthetic stages for the crab Neohelice granulata.

EXPERIMENT 2

The anesthetic tests were performed as described in Experiment 1. Terpinen-4-ol and nanoencapsulated TTO were used at concentrations of 300, 500, 1000, 2000, 3000, 5000, or 8000 µL L-1 for immersion tests. For the injection tests, nanoencapsulated TTO and terpinen-4-ol were used at doses of 20, 40, 60 µL, or 10, 20, 30, or 40 µL, respectively. In addition, they were also tested after diluting 10, 100, 1000, 10000, or 100000-fold in crustacean physiological solution for injection. Control experiments were performed using only nano blank.

STATISTICAL ANALYSIS

The results are presented as means ± standard error of the mean (SEM). Since most data were homoscedastic, as evident with Levene’s test, differences between groups were analyzed and detected using one-way analysis of variance (ANOVA) followed by Tukey’s test. The differences were considered to be statistically significant at p < 0.05. All analyses were carried out using the software Statistica 7.0 (Stat Soft, Tulsa, OK).

RESULTS

Most products tested did not produce any anesthetic efficacy for N. granulata, irrespective of the application method. EOLA and EOAT, when injected or used in oral gavage, caused autotomy and/or death (up to 30 min). However, TTO and eugenol produced anesthetic effects in the immersion test, but only at the highest concentration (8000 µL L-1) (p < 0.05) (Table II). Anesthesia induction and recovery with TTO and eugenol were observed within 20-30 min.

TABLE II
Method of exposure, induction and recovery times (in seconds), and anesthetic effects of essential oils and compounds tested in Neohelice granulata.

Induction of anesthesia was obtained with terpinen-4-ol and nanoencapsulated TTO (Figure 2). A faster anesthetic effect was observed with injection of 40 and 60 µL nanoencapsulated TTO, and 30 and 40 µL terpinen-4-ol (both without any dilution in physiological solution), with a maximum time of 407.4 s for anesthesia induction; however, injection of 20 µL terpinen-4-ol produced longer induction time (2361.2 s). Anesthetic recovery for crabs anesthetized with nanocapsulated TTO was rapid, with a maximum of approximately 540 s. However, the recovery time after treatment with terpinen-4-ol was lengthier, exceeding 30 min.

Figure 2
Induction and recovery times of terpinen-4-ol (a) and nanoencapsulated TTO (b) injected in Neohelice granulata. Stages of induction were observed according to Gardner (1997GARDNER C. 1997. Options for humanely immobilizing and killing crabs. J Shellfish Res 16: 219-224.) and Morgan et al. (2011). Maximum observation time for induction and recovery was 30 min. Data are presented as mean ± SEM (n = 5). Different letters indicate significant differences between concentrations, for the same stage (p < 0.05).

DISCUSSION

The present study is the first to report anesthetic activity in vivo for crabs using nanotechnological preparations, and demonstrated a low susceptibility of N. granulata to anesthesia by immersion with the tested EOs. Only TTO and eugenol (compound derived from clove oil) produced anesthetic effects by immersion, but both had long induction and recovery times. Eugenol produced 60% anesthetic efficacy in N. granulata up to 1800 s, and the recovery time was, on average, 1560 s at the highest tested concentration (8000 mL L-1), similar to observed using eugenol administered by immersion at 20000 µL L-1 in the crab Eriocheir sinensis, but only 20% of the animals were anesthetized (Hajek et al. 2009HAJEK GJ, CHOCZEWSKI M, DZIAMAN R AND KŁYSZEJKO B. 2009. Evaluation of immobilizing methods for the Chinese mitten crab, Eriocheir sinensis (Milne-Edwards). Electr J Pol Agric Univ 12: 18. ). However, exposure of the three-spot swimming crab, Portunus sanguinolentus, to clove oil added to sea water (200 µL L-1) produced a faster induction time, approximately 800 s, but recovery was slower, about 2460 s (Premarathna et al. 2016PREMARATHNA AD, PATHIRANA I, JAYANTHA RAJAPAKSE RPV AND PATHIRANA E. 2016. Evaluation of efficacy of selected anesthetic agents on blood-spotted crab (Portunus sanguinolentus). J Shellfish Res 35: 237-240.). These authors also suggested that clove oil (which is widely available and low cost), although it causes slow recovery, can be used as an anesthetic for crabs when prolonged anesthesia is required. Eugenol is an efficient anesthetic for white shrimp (L. vannamei); where 175 and 200 µL L-1 of eugenol was shown to induce deep anesthesia in larvae and sub-adults, respectively, within a maximum time of 500 s (Parodi et al. 2012PARODI TV ET AL. 2012. The anesthetic efficacy of eugenol and the essential oils of Lippia alba and Aloysia triphylla in post-larvae and subadults of Litopenaeus vannamei (Crustacea, Penaeidae). Comp Biochem Physiol C 155: 462-468.), but is not efficient for N. granulata. Interestingly, Morgan et al. (2001MORGAN J, CARGILL C AND GROOT E. 2001. The efficacy of clove oil as an anesthetic for decapod crustaceans. Bull Aquacult Assoc Can 101: 27-31.) demonstrated large differences in concentrations of eugenol used to induce anesthesia in three crayfish species (Cancer magister, Hemigrapsus oregonensis, and Pugettia producta), suggesting that differences in anesthetic efficiency could be because of the specificity of chemical receptors (Saydmohammed and Pal 2009SAYDMOHAMMED M AND PAL AK. 2009. Anesthetic effect of eugenol and menthol on handling stress in Macrobrachium rosenbergii. Aquaculture 298: 162-167.), which could also explain the low anesthetic efficacy of eugenol for N. granulata. Thus, the eugenol no can be considered an effective anesthetic agent for N. granulata via oral gavage, injected or by immersion.

Intravascular administration of EOs and eugenol was not effective and, in some cases, provoked autotomy and/or death. Although the exact cause of the crab mortalities in the present study was not determined, Minter et al. (2013MINTER LJ, HARMS CA, ARCHIBALD KE, BROADHURST H, BAILEY KM, CHRISTIANSEN EF, LEWBART GA AND POSNER LP. 2013. Efficacy of alfaxalone for intravascular anesthesia and euthanasia in blue crabs (Callinectes sapidus). J Zoo Wildl Med 44: 694-699.) related to limb autotomization occurs in an attempt to prevent excessive loss of hemolymph. The hemolymph, in the same way as the blood in vertebrates, is an aqueous medium and therefore is immiscible with most essential oils. According to Turner et al. (2011TURNER PV, BRABB T, PEKOW C AND VASBINDER MA. 2011. Administration of substances to laboratory animals: Routes of administration and factors to consider. J Am Assoc Lab Anim Sci 50: 600-613.), some oily substances may induce hemolysis when they are introduced intravenously. Despite their anesthetic ineffectiveness for N. granulata, EOs and eugenol injected at 50 µL may be suitable agents for euthanasia.

Silva et al. (2013SILVA LL, GARLET QI, BENOVIT SC, DOLCI G, MALLMANN CA, BÜRGER ME, BALDISSEROTTO B, LONGHI SJ AND HEINZMANN BM. 2013. Sedative and anesthetic activities of the essential oils of Hyptis mutabilis (Rich.) Briq. and their isolated components in silver catfish (Rhamdia quelen). Braz J Med Biol Res 46: 771-779.) verified the sedative properties of an immersion bath of terpinen-4-ol at 3 and 10 mg L-1, in silver catfish (R. quelen). The median induction times observed for terpinen-4-ol and nanoencapsulated TTO were comparable to those seen with injectable synthetic anesthetics in crustaceans, such as ketamine, xylazine, procaine, lidocaine, and alfaxalone (Brown et al. 1996BROWN PB, WHITE MR, CHAILLE J, RUSSELL M AND OSETO C. 1996. Evaluation of three anesthetic agents for crayfish (Orconectes virilis). J Shellfish Res 15: 433-435., Gardner, 1997GARDNER C. 1997. Options for humanely immobilizing and killing crabs. J Shellfish Res 16: 219-224., Quesada et al. 2011QUESADA RJ, SMITH CD AND HEARD DJ. 2011. Evaluation of parenteral drugs for anesthesia in the blue crab (Callinectes sapidus). J Zoo Wildl Med 42: 295-299., Minter et al. 2013MINTER LJ, HARMS CA, ARCHIBALD KE, BROADHURST H, BAILEY KM, CHRISTIANSEN EF, LEWBART GA AND POSNER LP. 2013. Efficacy of alfaxalone for intravascular anesthesia and euthanasia in blue crabs (Callinectes sapidus). J Zoo Wildl Med 44: 694-699.). It appeared that the injection of terpinen-4-ol and nanoencapsulated TTO did not cause large physiological alterations in the crabs, since there were no observed changes in autotomy or behavior, and no mortality was observed during or after recovery. Crustaceans respond differently to anesthesia than fish, possibly because their synaptic receptor sites are not affected by certain anesthetics (Ross and Ross 2008ROSS LG AND ROSS B. 2008. Anaesthetic and sedative techniques for aquatic animals. 3rd ed., Oxford, Blackwell, p. 236. ). In addition, much higher concentrations are required to anesthetize crustaceans than fish (Cunha et al. 2010aCUNHA MA, BARROS FMC, GARCIA LO, VEECK APL, HEINZMANN BM, LORO VL, EMANUELLI T AND BALDISSEROTTO B. 2010a. Essential oil of Lippia alba: a new anesthetic for silver catfish, Rhamdia quelen. Aquaculture 306: 403-406., b, Parodi et al. 2012PARODI TV ET AL. 2012. The anesthetic efficacy of eugenol and the essential oils of Lippia alba and Aloysia triphylla in post-larvae and subadults of Litopenaeus vannamei (Crustacea, Penaeidae). Comp Biochem Physiol C 155: 462-468., 2014). TTO at 200 µL L-1 is enough to anesthetize common carp (Cyprinus carpio) (Hajek 2011HAJEK GJ. 2011. The anaesthetic-like effect of tea tree oil in common carp Cyprinus carpio L. Aquacult Res 42: 296-300.) and gilthead seabream (Sparus aurata) (Golomazou et al. 2016GOLOMAZOU E, MALANDRAKIS EE, KAVOURAS M, KARATZINOS T, MILIOU H, EXADACTYLOS A AND PANAGIOTAKI P. 2016. Anaesthetic and genotoxic effect of medicinal plant extracts in gilthead seabream (Sparus aurata L.). Aquaculture 464: 673-682.), while 8000 µL L-1 of TTO was required to anesthetize 100% of N. granulata, which makes the use of TTO practically inviable due the volume used and elevated cost of procedure. In contrary, injections of non-diluted nanoencapsulated TTO and terpinen-4-ol provided rapid and reliable anesthesia induction in N. granulata at 40 and 60 µL, and 30 and 40 µL, respectively.

Based on these findings, it can be confirmed that N. granulata is neurosensitive to water soluble EO constituents, such as terpinen-4-ol (Hart et al. 2000HART PH, BRAND C, CARSON CF, RILEY TV, PRAGER RH AND FINLAY-JONES JJ. 2000. Terpinen-4-ol, the main component of the essential oil of Melaleuca alternifolia (tea tree oil), suppresses inflammatory mediator production by activated human monocytes. Inflamm Res 49: 619-626.) and some nanoencapsulated EOs (Assis et al. 2012ASSIS LM, ZAVAREZE ER, PRENTICE-HERNÁNDEZ C AND SOUZA-SOARES LA. 2012. Characteristics of nanoparticles and their potential applications in foods. Braz J Food Technol 15: 99-109.). Although Abbott (1970ABBOTT J. 1970. Absence of Blood-Brain Barrier in a Crustacean, Carcinus maenas L. Nature 225: 291-293.) demonstrated the absence of a hemolymph-brain barrier in crabs (Carcinus maenas), it is possible to speculate that there exists a more rigid barrier, which hinders the passage of some water insoluble molecules. The study conducted by Baldissera et al. (2017BALDISSERA MD, SOUZA CF, BOLIGON AA, GRANDO TH, DE SÁ MF, DA SILVA AS, STEFANI LM, BALDISSEROTTO B AND MONTEIRO SG. 2017. Solving the challenge of the blood-brain barrier to treat infections caused by Trypanosoma evansi: Evaluation of nerolidol-loaded nanospheres in mice. Parasitology 44: 1543-1550.) demonstrated that sesquiterpene nerolidol did not exhibit anti-parasitic effects in mice experimentally infected with Trypanosoma evansi, but when this compound was nanoencapsulated, it crossed the blood-brain barrier (BBB) and had 100% anti-parasitic efficacy. Thus, our results indicate that the nanoencapsulation of TTO allowed the passage of terpinen-4-ol through the more rigid barrier of crabs, and consequently, induced anesthesia. On the contrary, Maldonado et al. (1997MALDONADO H, ROMANO A AND TOMSIC D. 1997. Long-term habituation (LTH) in the crab Chasmagnathus: a model for behavioral and mechanistic studies of memory. Braz J Med Biol Res 30: 813-826.) pointed out that the absence of an endothelial hemolymph-brain barrier in crabs would be responsible for the increased action of compounds administered systemically. However, only water-soluble compounds, such as cloheximide actinomycin-D, angiotensin II, enkephalin, and serotonin were tested. Therefore, future studies should investigate the existence of a hemolymph-brain barrier in N. granulata using the Evans Blue dye.

A previous study conducted by Melo et al. (2010MELO NFS, GRILLO R, ROSA AH, FRACETO LF, DIAS FILHO NL, DE PAULA E AND ARAÚJO DR. 2010. Development and characterization of poli (L-lactide) nanocapsules containing benzocaine. Quim Nova 33: 65-69.) showed that nanoencapsulated benzocaine presented with increased solubility, thereby improving absorption and consequently potentiating its in vitro action. Consistent with this, Alonso (2004ALONSO MJ. 2004. Nanomedicines for overcoming biological barriers. Biomed Pharmacother 58: 168-172.) and De Jong et al. (2008) demonstrated that nanotechnology can facilitate the transfer of drugs through biological barriers through the reduction on size in the nanometric scale. Also, study conducted by Mistry et al. (2015MISTRY A, STOLNICK S AND ILLUM L. 2015. Nose-to-brain delivery: investigation of the transport of nanoparticles with different surface characteristics and size in excised porcine olfactory epithelium. Mol Pharm 12: 2755-2766. ) demonstrated that nanostructures with 20-200 nm presents a better capacity to cross the BBB, and the nanoencapsulated TTO used in this present study presents 150.2 nm, which also may explain the success of anesthesia with nanoencapsulated TTO.

In conclusion, most anesthetic protocols investigated in this study were not suitable for N. granulata, such as A. triphylla, L. alba and TTO essential oils, and the eugenol. Anesthesia by immersion appears to be inadequate, and injection of the above cited treatments are inappropriate and causes autotomy and/or death. As an alternative, we propose the use of nanoencapsulated EOs and isolated compounds, as TTO nanoencapsulated and terpinen-4-ol. We recommend the use of 20 and 40 µL of terpinen-4-ol and nanoencapsulated TTO, respectively, for short duration anesthesia of N. granulata. In summary, TTO nanoencapsulated and terpinen-4-ol can be considered effective as anesthetic to N. granulata for use to reduce or avoid stress during manipulation. In addition, future studies must be conducted to evaluate the effects of isolated compounds on the physiology of N. granulata.

ACKNOWLEDGMENTS

We thank A.L. Escarrone and B.D.P. Righi for initially helping us with the manipulation of crabs and preliminary tests. B. Baldisserotto, B.M. Heinzmann and B.O. Caron received Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) research fellowships, and C.F. Souza and M.D. Baldissera received Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) PhD fellowships.

REFERENCES

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Publication Dates

  • Publication in this collection
    25 June 2018
  • Date of issue
    Jul-Sep 2018

History

  • Received
    17 Nov 2017
  • Accepted
    25 Jan 2018
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