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PubMed2005

Evaluation of two genetic animal models in behavioral tests of anxiety and depression.

Anxiety- and depression-related disorders often appear associated and may be affected by common genetic factors. The inbred rat strains Lewis (LEW) and spontaneously hypertensive rats (SHR) and the outbred rat lines Floripa H and L, which were selectively bred for high and low locomotion in the central area of the open field (OF) test, respectively, have been proposed as experimental tools to study anxiety. The main goal of the present study was to characterize the behavior of these animals in two models of anxiety, elevated plus-maze (EPM) and OF, in two models of depression, forced swim test (FST) and tail suspension test (TST) and in their home-cages. Emotionality-related differences between LEW and SHR rats and between Floripa H and L rats were found in the EPM, OF and FST. Those lines showing low anxiety-like profiles in the EPM and OF (SHR and Floripa H) also showed low immobility in the FST. The TST failed to unveil any line differences. Factor analysis involving all tests revealed three independent factors with one of them associating anxiety-related measures from the OF and EPM to immobility in the FST. When observed in their home-cages, LEW and SHR rats showed no differences in general activity, but when acutely treated with imipramine (15mg/kg), only LEW rats were sensitive to its antidepressant effects. These results suggest the existence of a genetic link between two tests used in the screening of anxiolytic drugs and one test of antidepressant activity. Moreover, the LEW and SHR rat strains were shown to be an interesting model to study the comorbidity between anxiety- and depression-related disorders.

Animals↗
PubMed1975

Genetic studies on walking behavior in Drosophila melanogaster. I. Selection and hybridization analysis.

Rapid vs. slow types of walking behavior in Drosophila melanogaster were tested in response to light in a connected test-tube apparatus. The effect of selection for both types of behavior was clearly recognized after only a few generation. The heritability of the two traits of walking behavior was remarkably different; the former was estimated to be about 7%, the latter 26%. Walking behavior is possibly controlled by a major gene with the behavior manifesting slow response to light being dominant to that manifesting rapid walking behavior.

Animals↗
PubMed1998

Specific [3H]8-OH-DPAT binding in brain regions of rats genetically predisposed to various defense behavior strategies.

Distribution of 5-HT1A receptors was studied in rats genetically predisposed to two basic defense strategies--passive (freezing) or active (aggression) defensive behavior. Specific [3H]8-OH-DPAT binding was assayed in the brain structures of rat strains bred for 40 generations from Wistar stock for predisposition to freezing (catalepsy), and in wild rats bred for low and high aggression to humans. Considerable changes in [3H]8-OH-DPAT binding were found in the brain of rats with hereditary predisposition to catalepsy. A significant decrease in Bmax of specific receptor binding of [3H]8-OH-DPAT in the frontal cortex, and in the striatum as well as an increase in Kd in the hippocampus of cataleptic rats was shown. A clear-cut tendency to decrease of 5-HT1A receptor density was observed in the midbrain and hypothalamus of these rats. A comparison of wild Norway rats bred for aggressiveness against humans with those bred for the absence of affective aggressiveness showed a Bmax decrease without Kd change in the frontal cortex, hypothalamus, and amygdala of aggressive animals. It is hypothesized that 5-HT1A and probably 5-HT1A-like 5-HT7 serotonin receptors are involved in the mechanisms of both active and passive defense reactions, and the high expression of fear-induced defense is associated with their decrease in the frontal cortex. At the same time, the genetically determined preference for a certain defense behavior strategy depends either on the peculiarities of distribution of these receptor types in the brain regions or on some other types of serotonin receptors.

8-Hydroxy-2-(di-n-propylamino)tetralin↗
PubMed1991

Genetic differences in learning behavior in honeybees (Apis mellifera capensis).

Workers from colonies of Cape honeybees show marked phenotypic differences in performance in proboscis extension reflex (PER) conditioning. Analysis of these differences using parthenogenetic offspring groups permitted the estimation of genotypic values and revealed a high degree of genetic variability that is evident among related as well as unrelated bees. The results obtained from related groups are of particular importance, since they demonstrated the existence of strong genetic variability among individuals of the same colony. Quantitative analysis yielded high estimates of additive genetic effects and low estimates of dominance effects. Selection of individual workers resulted in an explicit increase in genetic variance of the next generation (G1). However, selection of bees from the parthenogenetic G1 generation, which was done to obtain parthenogenetic G2 offspring, did not lead to further improvement in selection. This observation suggests that recombination of linked genes underlying proboscis extension reflex was negligible during selection in parthenogenetic groups. Taken together with further behavioral analysis (Brandes and Menzel, 1990; Brandes et al., 1988), results from these quantitative genetic experiments suggest that additive genetic factors contribute significantly to variability among individuals for associative learning.

Animals↗
PubMed1975

Relative mating activity of the sexes in homokaryotypes of Drosophila persimilis from a Redwoods population.

Previous tests for mating activity of Drosophila persimilis homokaryotype KL (Klamath) and MD (Mendocino) chromosomal arrangements (northern California population: Redwoods) had shown KL to mate faster on the average than MD in homogamic tests. A strain (double-cross hybrid of four KL lines from the same population) with reliable high mating activity was developed for testing the sexes separately. Five pairs of KL-MD homokaryotype strains were chosen to be tested by the criterion that each pair had been derived from a separate wild KL/MD progenitor. Strains were crossed within arrangements in a diallelic design (20 inter- and five intrastrain crosses tested in 16 replicates per cross) to provide mating activity indices of four sets: KL females, KL males, MD females, MD males. Mating tests employed ten virgin experimental flies with ten tester (double-cross hybrid) flies of the opposite sex in 30-min observation periods. All flies were matured for 5 days at 25 degrees C before testing. Among parental strains, females were consistently higher in mating activity than males for both KL and MD arrangements. Most interstrain hybrids were heterotic, with KL and MD females not significantly different. However, hybrid MD males displayed greatest variation and had lowest mating activity, while KL males were the least variable and highest in mating activity. With heterosis in the hybrids, there was no predictability (additivity) from performance of parental strains to hybrid offspring. Mating activities of the two sexes were uncorrelated, indicating either that the sexes have independent genetic systems controlling mating activity or that the expression of the same genetic system is influenced by sex. Since the hybrid males of the two karyotypes displayed different courtship activity while the females were at about an equal level of receptivity, intrasexual selection among males is likely to be important in nature.

Alleles↗
PubMed1991

Quantitative morphological analysis of hippocampal structures in DBA1 and DBA2 inbred mice strains with genetically determined different shuttle box behavior: the mossy fiber system with reference data to the C3H strain.

The present work deals with morphological aspects which are likely related to a genetically determined learning behavior in the shuttle box paradigm. Subregions of the hippocampal mossy fiber system in two closely related inbred mice strains, DBA1 as a bad active avoider and DBA2 as a good one, are compared. Additionally, data derived from C3H (bad active avoider) studies are analyzed. Beside of certain structural similarities in DBA1 and DBA2 such as the elongation of infrapyramidal mossy fibers along the CA3 neurons this study pays attention to the topography of hilus and basal CA3 mossy fiber innervation.

Animals↗
PubMedDate not supplied

[Genetically determined variability in rat behavior and its biochemical correlates].

Using the combination of extremely high and low values of two independent behavioural variables (activity and frequency of defecation in open field) four groups of rats were selected with different CNS reactivity corresponding to the types of higher nervous activity described by I.P. Pavlov. These groups of rats revealed significant differences in reactivity to stress and drugs, in social behaviour and biochemical pattern. They may represent a useful tool for the research in experimental psychology, neurophysiology, psychopharmacology and other branches of science.

Animals↗
PubMed2026

Are There Any Effective Behavior Change Strategies for Communicating Genetic Risk in Obesity Prevention and Body Weight Reduction Interventions?

This systematic review examined how differences in intervention components may contribute to inconsistent findings in genetic risk communication studies, addressing obesity-related outcomes (e.g., weight reduction, nutrition behavior, exercise). The review was preregistered (PROSPERO #CRD42024524026) and followed PRISMA guidelines. Searches across eight databases identified 23 randomized controlled trials, covering 18 intervention trials. Risk of bias was assessed using the Risk of Bias 2 tool. A narrative synthesis was used to cluster studies by the content of intervention and control groups. Genetic risk communication alone (no behavioral counseling, addressing nutrition and exercise) or combined with phenotype-based risk was ineffective and sometimes counterproductive among low-risk individuals. When combined with personalized behavioral counseling, effectiveness improved, but only when compared to waitlist control groups or non-personalized behavioral counseling. Significant effects emerged in high-genetic risk subgroups within personalized behavioral counseling, using behavior change techniques such as problem-solving, feedback on behavior, self-monitoring, and environmental changes. The most promising results emerged from complex interventions integrating genetic risk communication into multiple sessions and combining numerous additional behavioral change techniques, such as social reward, cues/prompts, self-reward. Complex personalized interventions combining multiple behavior change techniques and prompting experiential genetic risk awareness show promise for improving weight, nutrition, and exercise-related outcomes.

Humans↗
PubMed2003

Conceptual and methodological issues in the genetics of mouse agonistic behavior.

Currently, 36 genes have been reported to affect offensive behavior in male mice. Potentially, these genes could be used to analyze the mechanism of this behavior. But there are methodological flies in this conceptual ointment. The studies with these genes varied in the genetic background, the maternal environments, the postweaning housing, the strain or type of opponent, and the type of test. The effects of each of these on the genetics of offense are reviewed with examples. It is concluded that between-study variation in these environmental or experiential circumstances may make it difficult to impossible to relate the effect of one genetic variant to another and to use these to identify and relate the pathways for gene effects on offensive behaviors. For this reason, standardization of these conditions is recommended.

Agonistic Behavior↗
PubMed1996

Quantitative genetic variation of odor-guided behavior in a natural population of Drosophila melanogaster.

Quantitative genetic variation in behavioral response to the odorant, benzaldehyde, was assessed among a sample of 43 X and 35 third chromosomes extracted from a natural population and substituted into a common inbred background. Significant genetic variation among chromosome lines was detected. Heritability estimates for olfactory response, however, were low, as is typical for traits under natural selection. Furthermore, the loci affecting naturally occurring variation in olfactory response to benzaldehyde were not the same in males and females, since the genetic correlation between the sexes was low and not significantly different from zero for the chromosome 3 lines. Competitive fitness, viability and fertility of the chromosome 3 lines were estimated using the balancer equilibrium technique. Genetic correlations between fitness and odor-guided behavior were not significantly different from zero, suggesting the number of loci causing variation in olfactory response is small relative to the number of loci causing variation in fitness. Since different genes affect variation in olfactory response in males and females, genetic variation for olfactory response could be maintained by genotype x sex environment interaction. This unusual genetic architecture implies that divergent evolutionary trajectories for olfactory behavior may occur in males and females.

Animals↗
PubMed1977

A genetic analysis of aggressive behavior in two strains of mice.

Examination of BALB/cJ and A/J mouse strains revealed marked differences in their levels of isolation-induced aggression. Using the dangler paradigm, we found that BALB/cJ males were uniformly aggressive, while A/J males showed no tendency to attack. Genetic analysis showed that the expression of aggressive behavior in the F1, F2, and backcross generations was consistent with the transmission of high aggressivity as a single, autosomal recessive trait. Although the data are consistent with a major-locus effect, more complex polygenic modes of inheritance have not been excluded.

Aggression↗
PubMed1997

Behavioral sensitization to ethanol: genetics and the effects of stress.

Some aspects of drug abuse syndromes may be influenced by sensitization to some drug effects. This enhancement of drug effect has been associated with prior drug exposure and with exposure to stressful stimuli. It has been postulated that sensitization to psychomotor stimulant drug effects influences sensitivity to drug reward. The drugs of abuse best characterized for sensitization phenomena include cocaine, amphetamine, and morphine. In general, ethanol's molecular mechanisms of action have been difficult to define relative to drugs with known receptor or transporter binding sites and, likewise, ethanol sensitization has been less thoroughly examined. Evidence supporting the existence of behavioral sensitization to ethanol, for genetic differences in the occurrence of ethanol sensitization, and for the influence of corticosterone on the development of ethanol sensitization is reviewed herein. There appear to be different genetic determinants of acute drug sensitivity and sensitization. Cross-sensitization between stress and ethanol suggest a potential role for hypothalamic-pituitary-adrenal (HPA) axis associated changes in ethanol sensitization, consistent with mechanisms likely contributing to sensitization to other abused drugs. Furthermore, glucocorticoid receptors appear to mediate both ethanol- and stress-induced sensitization to ethanol. A biological link between drug reward and drug sensitization involving HPA axis hormones may exist and, thus, study of the sensitization process may elucidate mechanisms relevant to drug abuse.

Animals↗
PubMed2005

Ontogeny in the family.

When ontogeny takes place in a family, and parents provide essential resources for development, the parents become an environmental component to the development of a wide range of offspring traits. Because differences among parents may partly reflect genetic variation, this environmental component contains genes and may itself evolve. Also, when offspring play an active role in family interactions, offspring become a social environmental component to parents, affecting their behavior in turn, which potentially results in reciprocal social selection. Thus, an evolutionary process of coadaptation to family life, additionally driven by conflicts of interests, may have shaped the expression and development patterns underlying infant behaviors. The complex genetics arising from family interactions can be formalized by extending standard quantitative genetic models. These models demonstrate how the explicit consideration of the family environment can profoundly alter both the expression and evolutionary response to selection of behaviors involved in family interactions. Behavioral genetic studies have begun to unravel the complex genetics underlying infant solicitation behaviors and parental provisioning, although many focus on one side of the interaction. A genetic analysis incorporating interactions among family members explicitly may be critical because the genes underlying the expression of parental provisioning indirectly affect offspring behaviors, and vice versa.

Child↗