Rat Park was a series of studies into drug addiction conducted in the late 1970s and published between 1978 and 1981 by Canadian psychologist Bruce K. Alexander and his colleagues at Simon Fraser University in British Columbia, Canada.
At the time of the studies, research exploring the self-administration of morphine in animals often used small, solitary metal cages. Alexander hypothesized that these conditions may be responsible for exacerbating self-administration. [1] To test this hypothesis, Alexander and his colleagues built Rat Park, a large housing colony 200 times the floor area of a standard laboratory cage. There were 16–20 rats of both sexes in residence, food, balls and wheels for play, and enough space for mating. [2] The results of the experiment appeared to support his hypothesis that improved housing-conditions reduce the consumption of morphine water. [1] This research highlighted an important issue in the design of morphine-self administration studies of the time, namely the use of austere housing-conditions, which confound the results. [3]
In Rat Park, the rats could drink a fluid from one of two drop dispensers, which automatically recorded how much each rat drank. One dispenser contained a sweetened morphine solution and the other plain tap water. Morphine solution was sweetened to reduce averse reaction to the taste of morphine; as a control, prior to morphine introduction, rats were offered a sweetened quinine solution instead.
Alexander designed a number of experiments to test the rats' willingness to consume the morphine. The Seduction Experiment involved four groups of 8 rats. [4] Group CC was isolated in laboratory cages when they were weaned at 22 days of age, and lived there until the experiment ended at 80 days of age; Group PP was housed in Rat Park for the same period; Group CP was moved from laboratory cages to Rat Park at 65 days of age; and Group PC was moved out of Rat Park and into cages at 65 days of age.
The caged rats (Groups CC and PC) took to the morphine instantly, even with relatively little sweetener, with the caged males drinking 19 times more morphine than the Rat Park males in one of the experimental conditions. The rats in Rat Park resisted the morphine water. They would try it occasionally—with the females trying it more often than the males—but they showed a statistically significant preference for the plain water. He writes that the most interesting group was Group CP, the rats who were brought up in cages but moved to Rat Park before the experiment began. These animals rejected the morphine solution when it was stronger, but as it became sweeter and more dilute, they began to drink almost as much as the rats that had lived in cages throughout the experiment. They wanted the sweet water, he concluded, so long as it did not disrupt their normal social behavior. [5] Even more significant, he writes, was that when he added naloxone, a drug which negates the effects of opioids, to the morphine-laced water, the Rat Park rats began to drink it.
In another experiment, he forced rats in ordinary lab cages to consume the morphine-laced solution for 57 days without other liquid available to drink. When they moved into Rat Park, they were allowed to choose between the morphine solution and plain water. They drank the plain water. He writes that they did show some signs of dependence. There were "some minor withdrawal signs, twitching, what have you, but there were none of the mythic seizures and sweats you so often hear about ..." [2]
The authors concluded that isolated cages, as well as female sex, caused an increased consumption of morphine. The authors advised that it is important to consider the conditions of testing, as well as the sex of the animals, when exploring self-administration of morphine. [1]
Studies that followed up on the contribution of environmental enrichment to addiction produced mixed results. A replication study found that both caged and "park" rats showed a decreased preference for morphine compared to Alexander's original study; the author suggested a genetic reason for the difference Alexander initially observed. [6] Another study found that while social isolation can influence levels of heroin self-administration, isolation is not a necessary condition for heroin or cocaine injections to be reinforcing. [7]
Other studies have reinforced the effect of environmental enrichment on self-administration, such as one that showed it reduced re-instatement of cocaine seeking behavior in mice through cues (though not if that re-instatement was induced by cocaine itself) [8] and another that showed it can eliminate previously established addiction-related behaviors. [9] Furthermore, removing mice from enriched environments has been shown to increase vulnerability to cocaine addiction [10] and exposure to complex environments during early stages of life produced dramatic changes in the reward system of the brain that resulted in reduced effects of cocaine. [11]
Broadly speaking, there is mounting evidence that the impoverished small cage environments that are standard for the housing of laboratory animals have undue influence on lab animal behavior and biology. [12] These conditions can jeopardize both a basic premise of biomedical research—that healthy control animals are healthy—and the relevance of these kinds of animal studies to human conditions. [13]
Bruce Petrie (1996), a graduate student of Alexander's, attempted to replicate the study and correct for the original studies on 20 rats using two different methods for measuring morphine consumption between conditions (which introduced a potential confound). [6] The study was not able to replicate the results, and the author suggested that strain differences between the rats Alexander's research group used could be the reason for this. [6]
There has been little subsequent interest in replicating the studies due to several methodological issues present in the originals. [14] Issues included the small number of subjects used, the use of oral morphine, which does not mimic actual conditions of use (and introduces a confound because of the bitterness of morphine), and the measurement of morphine consumption, which differed between conditions. Other problems included equipment failures, lost data and rat deaths. However, some researchers have shown an interest in "conceptual" replication to continue exploring the contribution of environmental and social enrichment to addiction. [14]
Journalist [15] [16] Johann Hari gave a popular TED Talk about the results of the study in 2015. In it, he interpreted the studies to suggest that biological underpinnings are not the cause of addiction, instead shifting the etiology to a need for healthy relationships. [17] The YouTube channel Kurzgesagt created and published a video based on Hari's book, which garnered over 19 million views. The channel later took down the video, stating that they improperly represented the evidence. [18]
Researchers have re-iterated that the results of Alexander's studies highlight issues with rat models kept in bare-bones lab environments, and help implicate the environment as a contributing factor to addiction. However, the media has overstated the studies' importance by suggesting it represents a paradigm shift in research, and that the environment is the only—or the key—factor in addiction. [3]
Dynorphins (Dyn) are a class of opioid peptides that arise from the precursor protein prodynorphin. When prodynorphin is cleaved during processing by proprotein convertase 2 (PC2), multiple active peptides are released: dynorphin A, dynorphin B, and α/β-neoendorphin. Depolarization of a neuron containing prodynorphin stimulates PC2 processing, which occurs within synaptic vesicles in the presynaptic terminal. Occasionally, prodynorphin is not fully processed, leading to the release of "big dynorphin". "Big dynorphin" is a 32-amino acid molecule consisting of both dynorphin A and dynorphin B.
4-Methylaminorex is a stimulant drug of the 2-amino-5-aryloxazoline class that was first synthesized in 1960 by McNeil Laboratories. It is also known by its street name "U4Euh" ("Euphoria"). It is banned in many countries as a stimulant.
Quinpirole is a psychoactive drug and research chemical which acts as a selective D2 and D3 receptor agonist. It is used in scientific research. Quinpirole has been shown to increase locomotion and sniffing behavior in mice treated with it. At least one study has found that quinpirole induces compulsive behavior symptomatic of obsessive compulsive disorder in rats. Another study in rats show that quinpirole produces significant THC-like effects when metabolic degradation of anandamide is inhibited, supporting the hypothesis that these effects of quinpirole are mediated by cannabinoid CB1 receptors. Quinpirole may also reduce relapse in adolescent rat models of cocaine addiction.
WIN 35,428 is a stimulant drug used in scientific research. CFT is a phenyltropane based dopamine reuptake inhibitor and is structurally derived from cocaine. It is around 3-10x more potent than cocaine and lasts around 7 times longer based on animal studies. While the naphthalenedisulfonate salt is the most commonly used form in scientific research due to its high solubility in water, the free base and hydrochloride salts are known compounds and can also be produced. The tartrate is another salt form that is reported.
18-Methoxycoronaridine, also known as zolunicant, is a derivative of ibogaine invented in 1996 by the research team around the pharmacologist Stanley D. Glick from the Albany Medical College and the chemists Upul K. Bandarage and Martin E. Kuehne from the University of Vermont. In animal studies it has proven to be effective at reducing self-administration of morphine, cocaine, methamphetamine, nicotine and sucrose. It has also been shown to produce anorectic effects in obese rats, most likely due to the same actions on the reward system which underlie its anti-addictive effects against drug addiction.
Brain stimulation reward (BSR) is a pleasurable phenomenon elicited via direct stimulation of specific brain regions, originally discovered by James Olds and Peter Milner. BSR can serve as a robust operant reinforcer. Targeted stimulation activates the reward system circuitry and establishes response habits similar to those established by natural rewards, such as food and sex. Experiments on BSR soon demonstrated that stimulation of the lateral hypothalamus, along with other regions of the brain associated with natural reward, was both rewarding as well as motivation-inducing. Electrical brain stimulation and intracranial drug injections produce robust reward sensation due to a relatively direct activation of the reward circuitry. This activation is considered to be more direct than rewards produced by natural stimuli, as those signals generally travel through the more indirect peripheral nerves. BSR has been found in all vertebrates tested, including humans, and it has provided a useful tool for understanding how natural rewards are processed by specific brain regions and circuits, as well the neurotransmission associated with the reward system.
The University of Minnesota runs a number of studies involving non-human primates, most notably research into drug addiction. The studies have attracted the attention of local and national animal rights groups, most especially the drug addiction studies of Marilyn Carroll, which she performs on primates, rats, and mice.
Cyprenorphine (M285), N-cyclo-propylmethyl-6,14-endoetheno-7α-(1-hydroxy-1-methylethyl)-6,7,8,14-tetrahydronororipavine, is an opioid drug. It is related to more well-known opioids such as buprenorphine, which is used as an analgesic and for the treatment of opioid addiction, and diprenorphine, which is used as an antidote to reverse the effects of other opioids. It is roughly 35 times as strong as nalorphine.
Animal psychopathology is the study of mental or behavioral disorders in non-human animals.
Psychological dependence is a cognitive disorder and a form of dependence that is characterized by emotional–motivational withdrawal symptoms upon cessation of prolonged drug use or certain repetitive behaviors. Consistent and frequent exposure to particular substances or behaviors is responsible for inducing psychological dependence, requiring ongoing engagement to prevent the onset of an unpleasant withdrawal syndrome driven by negative reinforcement. Neuronal counter-adaptation is believed to contribute to the generation of withdrawal symptoms through changes in neurotransmitter activity or altered receptor expression. Environmental enrichment and physical activity have been shown to attenuate withdrawal symptoms.
Environmental enrichment is the stimulation of the brain by its physical and social surroundings. Brains in richer, more stimulating environments have higher rates of synaptogenesis and more complex dendrite arbors, leading to increased brain activity. This effect takes place primarily during neurodevelopment, but also during adulthood to a lesser degree. With extra synapses there is also increased synapse activity, leading to an increased size and number of glial energy-support cells. Environmental enrichment also enhances capillary vasculation, providing the neurons and glial cells with extra energy. The neuropil expands, thickening the cortex. Research on rodent brains suggests that environmental enrichment may also lead to an increased rate of neurogenesis.
Conditioned place preference (CPP) is a form of Pavlovian conditioning used to measure the motivational effects of objects or experiences. This motivation comes from the pleasurable aspect of the experience, so that the brain can be reminded of the context that surrounded the "encounter". By measuring the amount of time an animal spends in an area that has been associated with a stimulus, researchers can infer the animal's liking for the stimulus. This paradigm can also be used to measure conditioned place aversion with an identical procedure involving aversive stimuli instead. Both procedures usually involve mice or rats as subjects. This procedure can be used to measure extinction and reinstatement of the conditioned stimulus. Certain drugs are used in this paradigm to measure their reinforcing properties. Two different methods are used to choose the compartments to be conditioned, and these are biased vs. unbiased. The biased method allows the animal to explore the apparatus, and the compartment they least prefer is the one that the drug is administered in and the one they most prefer is the one where the vehicle is injected. This method allows the animal to choose the compartment they get the drug and vehicle. In comparison, the unbiased method does not allow the animal to choose what compartment they get the drug and vehicle in. Instead, the researcher chooses the compartments.
Self-administration is, in its medical sense, the process of a subject administering a pharmacological substance to themself. A clinical example of this is the subcutaneous "self-injection" of insulin by a diabetic patient.
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Freezing behavior, also called the freeze response or being petrified, is a reaction to specific stimuli, most commonly observed in prey animals, including humans. When a prey animal has been caught and completely overcome by the predator, it may respond by "freezing up/petrification" or in other words by uncontrollably becoming rigid or limp. Studies typically assess a conditioned freezing behavior response to stimuli that typically or innately do not cause fear, such as a tone or shock. Freezing behavior is most easily characterized by changes in blood pressure and lengths of time in crouching position, but it also is known to cause changes such as shortness of breath, increased heart rate, sweating, or choking sensation. However, since it is difficult to measure these sympathetic responses to fear stimuli, studies are typically confined to simple crouching times. A response to stimuli typically is said to be a "fight or flight", but is more completely described as "fight, flight, or freeze". In addition, freezing is observed to occur before or after a fight or flight response.
PNU-99,194(A) (or U-99,194(A)) is a drug which acts as a moderately selective D3 receptor antagonist with ~15-30-fold preference for D3 over the D2 subtype. Though it has substantially greater preference for D3 over D2, the latter receptor does still play some role in its effects, as evidenced by the fact that PNU-99,194 weakly stimulates both prolactin secretion and striatal dopamine synthesis, actions it does not share with the more selective (100-fold) D3 receptor antagonists S-14,297 and GR-103,691.
Bruce K. Alexander is a psychologist and professor emeritus from Vancouver, BC, Canada. He has taught and conducted research on the psychology of addiction at Simon Fraser University since 1970. He retired from active teaching in 2005. Alexander and SFU colleagues conducted a series of experiments into drug addiction known as the Rat Park experiments. He has written two books about addiction: Peaceful Measures: Canada's Way Out of the War on Drugs (1990) and The Globalization of Addiction: A Study in Poverty of the Spirit (2008).
Addiction is a state characterized by compulsive engagement in rewarding stimuli, despite adverse consequences. The process of developing an addiction occurs through instrumental learning, which is otherwise known as operant conditioning.
Addiction vulnerability is an individual's risk of developing an addiction during their lifetime. There are a range of genetic and environmental risk factors for developing an addiction that vary across the population. Genetic and environmental risk factors each account for roughly half of an individual's risk for developing an addiction; the contribution from epigenetic risk factors to the total risk is unknown. Even in individuals with a relatively low genetic risk, exposure to sufficiently high doses of an addictive drug for a long period of time can result in an addiction. In other words, anyone can become an individual with a substance use disorder under particular circumstances. Research is working toward establishing a comprehensive picture of the neurobiology of addiction vulnerability, including all factors at work in propensity for addiction.
The Monkey Drug Trials of 1969 were a series of controversial animal testing experiments that were conducted on primates to study the effects of various psychoactive substances. The trials shed light on the profound effects of drug addiction and withdrawal in primates, pioneering critical insights into human substance abuse.
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