Thirst circuitry mapped in the brain
At a Glance
- Researchers mapped the wiring of the thirst center in the mouse brain.
- The findings provide a glimpse into the rules that govern how brain circuits regulate fluid intake.
Oka lab, CalTech
It’s important for your body to have plenty of fluids each day. Water helps you digest your food, absorb nutrients, and then get rid of the unused waste. Your body fluids are adjusted by feelings of thirst or satiety after you drink.
For decades, scientists have known that a brain region called the lamina terminalis controls these urges to drink or not. Neurons within three parts of the lamina terminalis—the subfornical organ (SFO), the organum vasculosum lamina terminalis (OVLT), and the median preoptic nucleus (MnPO)—work together to coordinate drinking behaviors. But precisely how this circuitry works has remained unknown.
Previous studies led by Dr. Yuki Oka of the California Institute of Technology showed that activation of nitric oxide synthase (NOS)-expressing neurons in the SFO triggers mice to start drinking, even when they are fully water-satiated. In this study, the team more fully mapped the neuronal connections underlying drinking and satiety in the mouse brain. The research was supported in part by the NIH’s National Institute of Neurological Disorders and Stroke (NINDS). Results were published in Nature on March 8, 2018.
The scientists first mapped the neurons in the three areas using a tracing technique. They found that NOS-expressing neurons in the SFO were directly connected to NOS-expressing neurons in the MnPO and OVLT. Moreover, in mice expressing genes that allow researchers to turn neurons on and off with light, the activation of NOS neurons in the SFO triggered the firing of their partners in the MnPO and OVLT.
Although activation of NOS neurons in any of the three areas triggered drinking in mice, further experiments showed that the thirst impulse required the presence of NOS-expressing neurons in the MnPO. In mice where these neurons were virtually eliminated, drinking behaviors were no longer stimulated by activating NOS-expressing SFO neurons. Loss of these MnPO neurons also greatly reduced the chance that mice would start drinking after activation of OVLT neurons. These findings suggest that MnPO neurons are necessary for stimulating drinking behaviors.
The scientists also found another set of neurons in the MnPO that sends inhibitory, or quieting, signals back to neurons in the SFO. These inhibitory neurons were marked by the presence of a gene called glucagon-like-peptide-1 (GLP1R). When these neurons were stimulated, dehydrated mice almost completely stopped drinking. In contrast, when GLP1R neurons were silenced, the dehydrated mice drank excessively.
Further experiments suggested that GLP1R neurons regulate thirst satiety based on the act of drinking or gulping, rather than on the body’s absorption of water. For instance, the GLP1R neurons only fired when mice drank fluids (saline, sugar water, and oil), but not when they licked a dry water spout or ate a watery gel. The neurons fired at different rates depending on how often the animals licked, not on the total amount of water consumed. The authors speculate that water absorption is detected through other neurons in the gastrointestinal system.
“The inhibitory signals we discovered are only active during the drinking action,” Oka says. “However, the feeling of satiety indeed lasts much longer. This indicates that the MnPO inhibitory neurons cannot be the only source of thirst satiety. This will be the subject for future study."
- Scientists Identify Thirst-Controlling Neurons
- High Salt Detected by Sour and Bitter Taste Cells
- Salt Taste Cells Identified
- Getting Enough Fluids
- Brain Initiative
References: Hierarchical neural architecture underlying thirst regulation. Augustine V, Gokce SK, Lee S, Wang B, Davidson TJ, Reimann F, Gribble F, Deisseroth K, Lois C, Oka Y. Nature. 2018 Mar 8;555(7695):204-209. doi: 10.1038/nature25488. Epub 2018 Feb 28. PMID: 29489747.
Funding: NIH’s National Institute of Neurological Disorders and Stroke (NINDS); California Institute of Technology; Searle Scholars Program; Mallinckrodt Foundation; the Okawa Foundation; McKnight Foundation; and Klingenstein-Simons Foundation.
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