Maternal aggression in rats: Changes over pregnancy and lactation in a sprague-dawley strain

Maternal aggression in a Sprague-Dawley strain of laboratory rat (Charles River CD) was explored from Day 1 after mating on Day 0 through Day 24 of lactation (L0-L24). Aggression toward unfamiliar male “intruders” during 10-min tests was low among nonpregnant, nonlactating females and during the first 10 days of gestation. Frequency of attack on intruders increased moderately but significantly by Gestation Day 16 (G16; Experiment 1) or G21 (Experiment 2), a prepartum phenomenon not previously reported in laboratory rats. Levels of aggression were highest, however, during the first 9 days of lactation, when attacks averaged more than 6 per 10-min session. Attacks declined sharply in frequency after L14 and by L24 did not exceed levels observed among nonpregnant females. Experiment 3 examined the importance of the test site (home cage with nest and pups, if any, vs unfamiliar cage without nest or pups) to agonistic behavior associated with pregnancy and lactation. Late pregnant females tested in a novel cage were not aggressive; however, females tested shortly after delivering their pups were highly aggressive, averaging over four attacks per 5-min session. In novel cage tests frequency of attack remained high through L4 but declined significantly by L7. These data are consistent with the hypothesis that maternal aggression at its onset is primarily under hormonal control, but becomes increasingly dependent upon external factors, presumably pup stimulation, during the postpartum period.     

Play-fighting differs from serious fighting in both target of attack and tactics of fighting in the laboratory rat Rattus norvegicus

Play-fighting is often difficult to differentiate from inhibited or immature serious fighting because both may utilize many of the same behavior patterns. In the rat the two behaviors involve different targets of attack. During play-fighting, snout or oral contact is directed at the opponent's nape of the neck, whereas during serious fighting, male residents mostly direct their bites at the intruder's rump. Although similar to those used in serious fighting, the behavior patterns used during play-fighting are modified to achieve the different targets of attack. Even though the tactics of attack and defense appear more adult-like with increasing age, the playful targets persist well into adulthood.     

Noninvolvement of testosterone in aggressive defense behavior in the male blind mole rat Spalax ehrenbergi

Blind mole rats (Spalax ehrenbergi) are solitary and aggressive subterranean rodents. Aggressive defense behavior in the mole rat functions to deter neighboring competitors from territory, food, and mates and includes seismic and odor signals. The aim of the present study was to determine whether the aggressive defense behavior displayed by male mole rats is testosterone dependent. Five behavioral variables were taken as being representative of such aggressive interaction: exposing teeth, biting, bulldozing movements of the head, soil blocking, and self‐grooming. We monitored male testosterone levels and aggressiveness throughout the annual cycle, which can be divided into three main climatic periods: cold and rainy (September–February); warm, during which the soil is still moist and easily excavated (March–May); and hot (June–August), when the soil is hard and dry. In a second experiment the effect of endogenous and exogenous testosterone on male aggressive defense behavior was determined before and after castration and following testosterone propionate replacement. We found fluctuations in male testosterone concentrations, with three peaks: in November, May, and August, one in each of the three climatic periods. However, these fluctuations did not correlate with male aggressive behavior, which remained constant throughout the year. Furthermore, because neither castration nor testosterone propionate replacement in castrated individuals affected their defense behavior, we suggest that such behavior in male mole rats is testosterone independent. The continuous excavation and maintenance of the mole rat’s underground tunnel system demands high energy expenditure year‐round and constant defense of territory sites and food caches from intraspecific rivals. Thus, although testosterone may fluctuate as a result of seasonal breeding cycles, constant high levels of aggressive defense throughout the year are crucial for the survival of the male mole rat in its solitary subterranean environment. Aggr. Behav. 27:64–72, 2001. © 2001 Wiley‐Liss, Inc.     

Agonistic versus amicable targets of attack and defense: Consequences for the origin,function, and descriptive classification of play-fighting

Play-fighting appears to involve the behavior patterns of attack and defense otherwise seen in serious fighting. The degree of similarity, however, depends on the body targets attacked and defended during these forms of fighting. For many taxa, including diverse mammalian families and some birds, the same targets are attacked and defended during both play-fighting and serious fighting. However, for several species of muroid rodents, the targets of play-fighting are not the same as those of serious fighting. In these cases, the tactics of attack and defense are also different. It is argued that for these muroid species the playful targets have arisen from amicable behavior (e.g., social investigation, greeting, allogrooming) rather than, as appears to be the case in so many other taxa, from agonistic behavior. These data strongly suggest that “play-fighting” has evolved from different precursors in different taxa and thus has multiple origins. Furthermore, these data have an important bearing on the universal applicability of many of the suggested functions of play-fighting and also on how such behavior is to be described and classified.     

Canine responses to familiar and unfamiliar humans

Dogs were observed during controlled approaches by their owners and by strangers. Significant differences between the dogs' responses to their owners and their responses to strangers were found. These results supported the popular belief that dogs respond differently to different persons, and not merely to different situations in which persons are usually encountered.     

Tyrosine hydroxylase activities in the brains of wild Norway rats and silver foxes selected for reduced aggressiveness towards humans

Tyrosine hydroxylase (TH) activity was measured in brains from Norway rats and silver foxes showing wild type aggressiveness and from their counterparts selected over 20-25 generations for reduced aggressiveness towards humans (tameness). TH activity in the brain stem and cortex was increased in tame animals of both species compared with aggressive counterparts. Selection increased hypothalamic TH activity in foxes, but decreased it in rats. There was no difference in TH activity in corpus striatum between the tame and aggressive animals. Fetal TH activity in the posterior part of the brain was higher in tame than aggressive rats at day 20 of embryogensis. Increased TH activity in the brain stem and cortex of adult aggressive rats was observed after treatment of their mothers with hydrocortisone on the days 16 and 18 of pregnancy. This elevation in TH activity was associated with attenuation of the defense behavior of aggressive rats. The data suggested that alterations in neural TH activity in tame rats and foxes may be part of the neurochemical basis of their behavioral phenotype which is developed by selection. © 1994 Wiley-Liss, Inc.     

Aggression,defense, and coping in humans

One way of identifying emotional behaviors across species, language, and cultures is to describe the “instrumental” effects of each particular behavior. Since aggression and defense may be instrumental they also represent coping behavior. The term coping is being used partly to indicate whether or not the behavior is successful and partly to describe how a situation is being handled (coping strategies). This review deals with how these behaviors are observed and quantified in humans and how they are linked to physiological changes. The internal state of the individual is decided by the expectancy of the outcome of a given situation, but each behavior strategy may have specific links to particular brain mechanisms and particular physiological effectors. © 1995 Wiley-Liss, Inc.     

Offensive and defensive bite-target topographies in attacks by lactating rats

The attacks by resident lactating Wistar rats on sexually naive conspecifics of both sexes were examined. Male and female intruders were equally attacked in terms of frequency and number of bites, but the topographies of biting seen in these encounters were different. Similarly to male-male agonistic interactions, females were attacked in a fashion which avoided bites to the head and snout (“offensive” attack), whereas males were frequently bitten on such vulnerable regions (“defensive” attack). This dichotomy in bite pattern suggests that different motivations and functions underlay maternal aggression in these situations. The defensive attack on males may be a deterrent to infanticide since only male intruders counterattack lactating females and kill their pups. The attack on females may be concerned with resource competition.     

Relationship between mousekilling and conspecific aggression in the male rat

In order to investigate the relationships between mousekilling and conspecific aggression, behavioral variables of killer and nonkiller rats were compared in a “resident-intruder” paradigm, in resident as well as in intruder animals. The occurrence of offensive items (offensive sideways, attack) was significantly higher in killer rats when they were residents; their corresponding opponents displayed more defensive behaviors. No significant difference in aggressive behaviors was noted when the comparison was done in the intruders. These results and those of previous studies suggest that there is a correlation between mousekilling and intraspecific offensive behaviors. Some similarities in the situations where both behaviors are elicited–eg, introduction of an unfamiliar intruder into a familiar environment–may contribute to the existence of such a correlation and the possibility of common mechanisms underlying both behaviors is discussed.