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PubMed1998

Nicotine-induced grooming: a possible dopaminergic and/or cholinergic mechanism.

The ability of nicotine, to induce grooming in rats was studied. Grooming was induced by i.p. injection of different doses (0.0675-0.5 mg/kg) of nicotine to rats. The effect was dose-dependent. However, the response was decreased with increasing doses of the drug from 0.25-0.5 mg/kg. Administration of the dopamine (DA) D1/D2 receptor agonist apomorphine (0.025-5 mg/kg, i.p.) also caused grooming in a dose-dependent manner. High doses of apomorphine (0.1-0.5 mg/kg, i.p.) also induced a lower degree of response. Combination of a low dose of nicotine (0.0675 mg/kg) with different doses of apomorphine did not show any interaction. However, there was an interaction between a high dose of nicotine and apomorphine. Thus, combination of a higher dose of nicotine (0.125 mg/kg) with apomorphine, reduced apomorphine-induced grooming. The muscarinic receptor antagonist atropine (5 and 10 mg/kg), peripheral nicotinic receptor antagonist hexamethonium (5 and 10 mg/kg), central nicotinic receptor antagonist mecamylamine (1 and 3 mg/kg) and D1 DA receptor antagonist SCH23390 (0.05 and 0.1 mg/kg) all decreased the response to nicotine. Atropine, mecamylamine and SCH23390 by themselves reduced spontaneous grooming. It is concluded that nicotine elicits grooming indirectly through a possible D1 dopaminergic mechanism. However, muscarinic and nicotinic cholinergic mechanism(s) may be involved.

Animals↗

PubMed2002

Reproductive experience influences grooming behavior during pregnancy in rats.

The pregnancy-induced increase in self-licking observed in rats is important for mammary gland development and lactation. Reproductive experience has epidemiologial implications such as a decrease in the incidence of mammary gland cancer in women and it also influences various behavioral, neurochemical and endocrine parameters. The aim of the present study was to investigate the influence of reproductive experience on grooming behavior patterns during pregnancy in rats. Self-grooming behavior was measured in age-matched virgin, primi- and multigravid (days 7, 8, 9, 19, and 20 of pregnancy) rats. General grooming (head, forelimbs and shoulders) was not significantly different among virgin, primi- and multigravid rats during pregnancy. Confirming previous work, pregnant rats spent significantly more time in specific grooming (mammary glands, nipple lines, genital and pelvic regions) than did virgin animals. In addition, self- licking of mammary glands was significantly increased in multi- as compared to primigravid rats on days 8, 9, 19 and 20 of pregnancy. The increase in mammary gland grooming observed in multigravid rats appears to be a consequence of previous reproductive experience. These data show that reproductive experience modulates mammary gland grooming during pregnancy, possibly contributing to successful reproduction.

Analysis of Variance↗

PubMed1980

Substance P elicited grooming in the mouse: behavioral and pharmacological characteristics.

Substance P undercapeptide produces intense grooming after central injection. To characterize further this syndrome at behavioral and psychopharmacological level: (a) substance P elicited grooming was compared to spontaneously occurring grooming for their respective behavioral characteristics, and (b) a variety of centrally active substances were injected in an attempt to modify the normal occurrence of the grooming syndrome. Manipulations of opioid systems did not affect grooming, nor did a variety of other peptides. However, central injections of neurotensin significantly inhibited grooming. This interaction may represent a functional behavioral correlate of the established neuroanatomical interactions of the above substances.

Animals↗

PubMedDate not supplied

[Nonspecific grooming in rats during the solution of an extrapolation task].

Grooming behavior in laboratory brown rats was analysed in the course of extrapolation task solving. Cases of task solution (correct and incorrect) were compared with those when animal "refused" to turn round the screen during search of food bait. In latter cases grooming episodes were more numerous, their latency and duration being higher than during former cases. At the same time the latest stages of experiment (when 8-13 trials a day twice a week were presented) were characterized by more frequent grooming occurrence as well as by longer latencies and duration of grooming episodes. When rats were given I trial a day with one week intervals grooming incidence as well as "refusals" occurrence decreased. The possible participation of animal grooming in arranging the defense reactions against excessive and inadequate activity is discussed.

Animals↗

PubMed1993

[Effect of reserpine on grooming parameters in rats].

The analysis of data of the graphic registration of grooming showed that prolonged injections of reserpine (2.5 mg/kg of weight) induce phasic changes on the stereotype grooming movements. During the period when the noradrenergic influence is pronounced (the 1st day of injection of reserpine) grooming movements are inhibited, their duration is diminished, especially of washing movements. During the period when the noradrenergic influence is weakened (the 2nd and the 3rd days after injections) grooming movements are activated and the duration of every movement is prolonged; moreover, they unite into long "chains" of movements. During the period when dopaminergic influence is weakened (the 4th and the 5th days) tremor ensues, grooming is depressed except for "shaking-down" movements whose quantity and duration increase. Reserpine does not influence in any noticeable degree on h the frequency of grooming movements of adult rats.

Animals↗

PubMed1996

Thyrotropin releasing hormone injected into the nucleus accumbens septi selectively increases face grooming in rats.

The effect of unilateral injection of peptides into the nucleus accumbens septi (NAS) on subcategories of grooming behavior was studied in male rats. The peptides used were: thyrotropin releasing hormone (TRH), luteinizing hormone releasing hormone (LHRH) and corticotropin releasing hormone (CRH). Male rats (Holtzman strain, 240-270 g body weight) injected with progressive doses of TRH (100, 200 and 400 ng) at 5-day intervals were compared with the control state (injection of artificial cerebrospinal fluid, CSF). A selective increase in face grooming was observed with the 100 ng (49.78 +/- 6.11, N = 18) and 200 ng (50.29 +/- 7.72, N = 17) doses of TRH (P < 0.05 vs CSF injection, 26.94 +/- 3.64, N = 18). Face grooming increased further with the 400 ng dose (55.19 +/- 8.26, N = 16, P < 0.01), but a dose-response curve could not be obtained at the dose range used. Flank scratching, head, body and genital grooming were not altered by the TRH injection, but the rearing behavior was inhibited (10.33 +/- 1.56; N = 18; 10.76 +/- 1.77, N = 17; 12 +/- 2.06, N = 16) (P < 0.05 for all doses vs controls, 20.61 +/- 2.81, N = 18). The rats that received LHRH (75 ng, N = 16) and CRH (100 ng, N = 14) did not show behavioral changes when compared with their control states. The results show that injection of TRH into the NAS, but not the injection of LHRH or CRH, selectively increases face grooming without affecting other subcategories of grooming at the doses used, and appears to link this peptide with the neural substrate of stereotyped behavior.

Animals↗

PubMed1997

Grooming down the hierarchy: allogrooming in captive brown capuchin monkeys, Cebus apella

Observations of captive female brown capuchin monkeys in five groups revealed that grooming is primarily the occupation of dominant females at both the individual and dyadic levels. When categorized according to rank class, alpha females were the only class to perform significantly more grooming than they received. These results are inconsistent with reports on vervets, baboons and macaques, and suggest that grooming in capuchin monkeys may have different functions from those reported for cercopithecine primates. A dyadic analysis revealed, however, that grooming occurred more often between closely ranked females, similar to what is seen in several Old World monkey species. Therefore, some aspects of grooming in capuchins are similar to that seen in Old World monkeys, but the way they distribute grooming is different, which may prompt a re-evaluation of current theories regarding the social function of allogrooming in non-human primates.

Journal Article↗

PubMed1978

Biosocial functions of grooming behavior among the common Indian langur monkey (Presbytis entellus).

An intensive study of the Indian langur monkey (Presbytis entellus) reveals an interplay between biological and social processes. This study which involved captive animals and over 1,500 observation hours suggests that grooming behavior alone cannot be used to measure status differences between the sexes, nor as a means to understand how pathogens carried by ecto-parasites are controlled. It is shown that the type of grooming exhibited in an interactional setting and the region of the body presented by one animal to another for grooming is often determined by the immediate social events and by the nature of the relationship existing between the participants. For these Colobine langur monkeys grooming behavior not only facilitates integration but it also enables an animal to manipulate a tense situation into a peaceful one. Without reference to many of the other patterns of behavior which only relatively, not absolutely differentiate age and sex classes, grooming behavior cannot be entirely understood.

Age Factors↗

PubMed1985

Early ontogeny of face grooming in mice.

A U-shaped function of behavioral growth characterizes the early ontogeny of face grooming in mice. In the first few postnatal days (0-100 hr), mice groom their face by using temporally isolated strokes, or bouts of strokes, which vary in amplitude and symmetry. Later on (100-200 hr), bouts disappear, asymmetry is eliminated, and the amplitude of strokes is gradually restricted; the infants engage in stereotyped, double-handed, temporally isolated strokes. Finally (200-300 hr), bouts reappear, including both short and long, symmetrical and asymmetrical, strokes. These changes, are accompanied by unidirectional changes such as an increasing participation of the trunk, the neck, and the head in grooming, which lead to the flexible organization of face grooming seen in adults. Instead of describing development in terms of emerging unitary "acts," we have recorded from high-speed films three simultaneous aspects of movement: the movements of the separate limb and body segments, the resultant paths which are traced by the forepaws, and the paths of contact which are traced on the face. This method of description discloses (a) reversible changes, and (b) a change in the relative stability of each of these aspects of face grooming, in the course of early ontogeny.

Animals↗

PubMed1981

Swim-induced grooming in mice is mediated by a dopaminergic substrate.

Grooming induced in mice after a period of swimming was potently and dose-dependently blocked by neuroleptics. The order of potency of the neuroleptics was spiroperidol greater than haloperidol greater than cis-flupenthixol greater than pimozide greater than chlorpromazine greater than thioridazine. The trans isomer of flupenthixol was inactive at 40 microM/kg. The alpha-adrenergic receptor antagonists, phentolamine and phenoxybenzamine, and the catecholamine synthesis inhibitor, alpha-methyl-p-tyrosine were essentially without effect on the grooming behaviour. Amitriptyline inhibited grooming behaviour only in doses which severely affected the animals motor function. Fluoxetine was without effect. Cis-flupenthixol was less active in inhibiting grooming in animals chronically treated with haloperidol than in control animals, indicating the presence of supersensitive dopamine receptors. The data indicate that swim-induced grooming in mice is mediated via dopaminergic systems.

Adrenergic alpha-Antagonists↗

PubMed2002

Leaf-grooming by a wild chimpanzee in Mahale.

During the course of systematic observations of the leaf-grooming behavior by the chimpanzees (Pan troglodytes) of the Mahale Mountains National Park, Tanzania, I recovered a louse from a leaf "groomed" by an adult male chimpanzee after a typical leaf-grooming session. During the leaf-grooming session I observed a small object on his lower lip. He picked up a leaf, transferred the small object from his lip to the leaf, folded the leaf and crushed the folded side of the leaf with his thumb. I present this observation as further evidence of the "squashing ectoparasites" hypothesis for leaf-grooming.

Animals↗

PubMed1986

Major tranquillizers can be distinguished from minor tranquillizers on the basis of effects on marble burying and swim-induced grooming in mice.

The effects of psychotropic compounds on grooming and burying were compared in mice. Burying behaviour was provoked by glass marbles and grooming was observed after 3 min swimming. Compounds with minor tranquilizing properties, such as diazepam, chlordiazepoxide, flunitrazepam, clonazepam, meprobamate and ethyl alcohol, were more effective in reducing burying than grooming. Drugs with an anticholinergic effect, e.g. scopolamine and atropine were also more effective against burying. A number of neuroleptic drugs, such as haloperidol, chlorpromazine, perphenazine and trifluperidol reduced grooming more effectively than burying. Non-selective inhibitory effects were observed with clozapine, thioridazine, diphenhydramine, imipramine, mianserin and apomorphine. It is concluded that, with certain limitations, the burying-grooming test described offers a simple tool for identifying novel compounds as potential major or minor tranquilizers.

Animals↗

PubMed1992

Effect of 5-HT1C and 5-HT2 receptor stimulation on excessive grooming, penile erection and plasma oxytocin concentrations.

Serotonin (5-HT) receptor agonist-induced excessive grooming, penile erection and oxytocin secretion were studied in chronically cannulated freely moving rats. The 5-HT1C receptor agonist, m-chlorophenylpiperazine (m-CPP), which also binds to other 5-HT receptors, produced dose-dependent excessive grooming, penile erection and increases in circulating oxytocin concentrations. Maximal responses for excessive grooming and penile erection occurred at 0.3-0.6 mg/kg i.v. m-CPP. Higher doses (0.9-2.5 mg/kg i.v.) caused further increases in oxytocin concentrations, but attenuated both behavioral responses. All three responses to m-CPP (0.6 mg/kg) were attenuated by antagonists with high affinity for the 5-HT1C receptor site (mianserin, LY-53857 and metergoline), but not by the 5-HT2 receptor antagonist ketanserin. The 5-HT2/5-HT1C agonist, 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane (DOI), increased plasma oxytocin concentrations only. After ketanserin pretreatment, DOI caused penile erection and diminished the oxytocin response. All responses to DOI were blocked completely by pretreatment with LY-53857 plus ketanserin. Excessive grooming and penile erection showed significant bimodal correlations with the oxytocin response. These data suggest that stimulation of 5-HT1C receptors induces excessive grooming, penile erection and increased oxytocin secretion. Stimulation of 5-HT2 receptors causes a further increase in plasma oxytocin concentration, but inhibits both behavioral responses.

Analysis of Variance↗

PubMed1992

Suppressive effect of the dopamine D2 receptor agonist B-HT 920 on rat grooming.

The effect of the D2 agonist B-HT 920 was examined on three behavioural models of induced grooming in the rat. B-HT 920 potently inhibited the grooming elicited by a novel environment, whereas it stimulated the stretching-yawning syndrome. Pretreatment with the selective dopamine D2 receptor antagonist, sulpiride, reversed the phenomenon. When B-HT 920 was administered to rats before water immersion, it similarly antagonized total grooming; wet-dog shakes, detected in these same animals, were potently inhibited. Finally, B-HT 920 displayed inhibitory activity towards adrenocorticotropin hormone-induced excessive grooming. On the basis of these effects, the role of D2 receptor subtypes in the modulation of grooming is discussed.

Analysis of Variance↗

PubMed1986

Character of (D-Phe-7) ACTH4-10-induced excessive grooming.

Rats receiving (D-Phe-7) ACTH4-10 exhibited excessive grooming during the first half of the hour-long observation period. This resulted in total grooming scores of about one-half of those produced by the longer ACTH fragments, ACTH1-24 or ACTH1-16 NH2. The excessive grooming induced by (D-Phe-7) ACTH4-10 was due to an enhancement of duration of grooming bouts and not to an increase in the frequency of occurrence. Furthermore, the neuropeptide-induced excessive grooming was eliminated by prior treatment with naloxone.

Adrenocorticotropic Hormone↗

PubMed1992

Effect of the D2-autoreceptor agonist B-HT 958 on both spontaneous and ACTH-induced stretching, yawning and grooming in the rat.

The D2 autoreceptor agonist B-HT 958, intraperitoneally injected into Wistar male rats in a novel environment, significantly increased stretching and yawning (SY) while inhibiting grooming. Pretreatment with the D2 antagonist sulpiride reversed these effects, antagonizing SY and restoring grooming. Similarly, when B-HT 958 was administered to rats in their home cages, it elicited SY and abolished grooming; moreover, when administered before the i.c.v. injection of adrenocorticotropin hormone, dose-dependently enhanced SY and strongly antagonized the typical syndrome of intensified grooming induced by the peptide. The possible relationship between SY and grooming and the involvement of D2 autoreceptors are discussed.

Adrenergic alpha-Agonists↗

PubMed1982

Conditioned aversion to a taste perceived while grooming.

Four experiments were conducted to determine how the characteristics of conditioned taste aversion (CTA), as described from studies conducted in the drinking and feeding contexts, applied in the grooming context. In Experiment 1, sodium saccharin was mixed with a "neutral-tasting" jelly and applied to the fur of male Sprague-Dawley rats. Rats injected with LiCl after the applications strongly avoided saccharin solutions in subsequent 1-hr, 2-choice (Saccharin solution vs water) drinking tests, whereas rats injected with NaCl or given plain jelly on the fur showed only an initial neophobic response to the saccharin solution. Thus, the taste of saccharin was perceived while grooming and the CTA formed in the grooming context generalized to drinking. In experiments 2-4, we obtained evidence that: (a) rats discriminated between one intensity of saccharin applied to the fur and another used in the test solution; and (b) rats differentiated between qualities of the two tastants applied to the fur in that saccharin overshadowed NaCl; and (c) taste qualities were more important than toxic properties when two stimuli (Saccharin, LiCl) were used (saccharin overshadowed NaCl in subsequent drinking tests). We speculate that taste, while grooming might play a role in social communication in some vertebrates. Further, CTA and grooming might have uses in rodent control (e.g., in agricultural situations) not previously considered such as in delivering a non-attractive, low-salience toxin so that the taste of the crop overshadows that of the bait, and induces crop aversion.

Animals↗

PubMed1984

Disparity between formation of conditioned flavor aversions and neophobia during grooming in rats and mice.

Mice (Mus musculus) allowed to groom a paste containing saccharin from their fur before injection with lithium chloride displayed a saccharin aversion in subsequent drinking preference tests. No attenuation of neophobia was observed in mice grooming saccharin because the animals failed to display a neophobia towards saccharin in drinking tests. Rattus norvegicus displayed neophobia towards saccharin in two- and single-bottle drinking tests but this neophobia was not attenuated by grooming experience with the saccharin paste. Rats apparently learn that if a taste is hazardous in the grooming context it is also likely hazardous in an appetitive context. Learned safety in grooming, however, does not generalize into the appetitive context. The results support the view that neophobia and learned taste aversion depend upon different mechanisms.

Animals↗