Attenuated frontal and sensory inputs to the basal ganglia in cannabis users
Laura Blanco‐Hinojo, Jesus Pujol, Ben J. Harrison, Dídac Macià, Albert Batalla, Santiago Nogué, Marta Torrens, Magı́ Farré, Joan Deus, Rocío Martín‐Santos
Addiction Biology March 3, 2016 DOI: 10.1111/adb.12370 via OpenAlex
Summary
Chronic cannabis use is associated with reduced motivation, and this study examined how it affects functional connectivity between the basal ganglia and brain regions involved in internal (frontal cortex) and external (sensory cortices) motivation signals. Resting-state fMRI in 28 chronic cannabis users and 29 controls showed that cannabis exposure attenuated the positive correlation between the striatum and limbic frontal-basal ganglia circuits, and attenuated the negative correlation between the striatum and the fusiform gyrus, which is important for recognizing significant visual features. These connectivity alterations were linked to lower arousal in response to affective pictures. Changes tended to normalize after one month of abstinence, indicating that cannabis impairs fine-tuning of the motivation system, but this effect is reversible.
Study at a glance
| Characteristics | Observational cohort Peer reviewed |
|---|---|
| Sample size | 57 |
| Population | Chronic cannabis users and controls |
| Duration | One month of abstinence |
| Topics | Cannabis |
| Keywords | Basal ganglia Frontal lobe Inferior frontal gyrus Psychology Neuroscience |
| Citations | 52 |
| Key finding | Chronic cannabis use attenuates frontal and sensory inputs to the basal ganglia, impairing responsiveness to both internal and external motivation signals, with a tendency to normalize after abstinence. |
Abstract
Heavy cannabis use is associated with reduced motivation. The basal ganglia, central in the motivation system, have the brain's highest cannabinoid receptor density. The frontal lobe is functionally coupled to the basal ganglia via segregated frontal-subcortical circuits conveying information from internal, self-generated activity. The basal ganglia, however, receive additional influence from the sensory system to further modulate purposeful behaviors according to the context. We postulated that cannabis use would impact functional connectivity between the basal ganglia and both internal (frontal cortex) and external (sensory cortices) sources of influence. Resting-state functional connectivity was measured in 28 chronic cannabis users and 29 controls. Selected behavioral tests included reaction time, verbal fluency and exposition to affective pictures. Assessments were repeated after one month of abstinence. Cannabis exposure was associated with (1) attenuation of the positive correlation between the striatum and areas pertaining to the 'limbic' frontal-basal ganglia circuit, and (2) attenuation of the negative correlation between the striatum and the fusiform gyrus, which is critical in recognizing significant visual features. Connectivity alterations were associated with lower arousal in response to affective pictures. Functional connectivity changes had a tendency to normalize after abstinence. The results overall indicate that frontal and sensory inputs to the basal ganglia are attenuated after chronic exposure to cannabis. This effect is consistent with the common behavioral consequences of chronic cannabis use concerning diminished responsiveness to both internal and external motivation signals. Such an impairment of the fine-tuning in the motivation system notably reverts after abstinence.