Biology subjects

Shah, D. P.

Publications and source records attributed to Shah, D. P..

4 recordsLinked to original sources

bioRxiv2024

Acute restraint stress and pain modulation depend on the interaction between the periaqueductal gray and the lateral septum

Acute restraint stress is known to cause analgesia in humans and laboratory animals, but the mechanisms are unknown. Recently, we have shown that a multi-nodal circuitry between the dorsal lateral septum (dLS)-lateral hypothalamic area (LHA)-rostral ventromedial medulla (RVM) plays an instructive role in restraint stress-induced analgesia. We found that the LS neurons are activated when mice struggle to escape the restraint, and we wondered about the origin of the escape signals. Hence, we performed retrograde viral labeling from the LS and found that the ventrolateral periaqueductal gray (vlPAG), a known anatomical substrate for escape behaviors, provides inputs to the LS. Through anatomical, behavioral, and in-vivo fiber photometry, we show that the PAG and LS neurons are synaptically connected; activation of either PAG or the post-synaptic LS neurons is sufficient to cause analgesia and sufficiently cause hyperalgesia. Moreover, we found that the LS neurons that receive inputs from PAG send axonal projections to the LHA. Together, we found that the vlPAG neurons encoding nociceptive and escape behaviors provide synaptic inputs to the dLS-LHA-RVM circuitry to mediate acute restraint stress-induced analgesia. Significance statementForced restraint causes stress, and this paradigm has been used in the laboratory to study the physiological effects of stress, including pain modulation. The dorsal lateral septum (LS) has been shown to mediate restraint-mediated stress and analgesia. It is unknown what signals encoded in the LS allow it to instruct stress and pain. A novel neural pathway between the periaqueductal gray (PAG) and LS is activated when mice try to escape the restraint. Repeated activity in the PAG-LS circuitry due to the inescapability of the restraint causes stress and analgesia

neuroscience↗

bioRxiv2024

Rostral ventromedial medulla (RVM) projects to the lateral hypothalamic area (LHA) to drive aversion and anxiety

Neurons in the LHA are critical drivers of behavioral and physiological responses to acute and chronic stress. However, the roles of the specific pre-synaptic inputs to the LHA in driving stress and resultant physiological effects are yet to be fully understood. Here, taking advantage of mouse viral genetics, rabies tracing, optogenetics, chemogenetics, and fiber photometry, we show that the excitatory projections from the RVM to LHA drive stress-induced anxiety. This is a surprising finding since, traditionally, RVM has been studied in the context of opioidergic pain modulation through its inhibitory projections to the spinal cord. We find that the LHA neurons receiving inputs from the RVM, when activated, do not alter the nociceptive thresholds yet are sufficient to drive anxiety-like behaviors. These LHA neurons are recruited by acute restraint, which is known to cause stress. On the other hand, the LHA-projecting RVM neurons are responsive to both noxious thermal stimuli and acute restraint, promoting stress-induced anxiety, yet with no effect on pain thresholds. Together, we found an ascending neural pathway between RVM and LHA that mediates stress-induced anxiety. Significance statementThere is a strong correlation between pain and anxiety. However, the underlying neural mechanisms are poorly understood. Here, we reveal a novel neural pathway between the rostral ventromedial medulla (RVM) and lateral hypothalamus (LHA) that can potentially convert painful experiences into stress and anxiety. The traditional role of RVM is opioidergic modulation of pain. However, here we show that in addition to nociception, RVM neurons can play an essential role in the affective-motivational components of pain.

neuroscience↗

bioRxiv2024

An Intra-brainstem Circuit for Pain-induced Inhibition of Itch

Pain and itch are unpleasant and distinct sensations that give rise to behaviors such as reflexive withdrawal and scratching in humans and mice. Interestingly, it has been observed that pain modulate itch through the neural circuits housed in the brain and spinal cord. However, we are yet to fully understand the identities of and mechanisms by which specific neural circuits mediate pain-induced modulation of itch. Independent studies indicate that brainstem nuclei such as the lateral parabrachial nucleus (LPBN) and rostral ventromedial medulla (RVM) are important for the suppression of itch by painful stimuli. Here, using mouse and viral genetics, rabies tracing, chemogenetics, and calcium imaging, we show that the synaptic connections between LPBN and RVM plays an instrumental role in the interactions between pain and itch. Notably, we found that the LPBN neurons that express the gene encoding the substance P receptor, Tacr1 (LPBNTacr1), synapse onto Tacr1-expressing RVM neurons (RVMTacr1). The RVMTacr1 neurons were found to be nociceptive, sufficient for inhibiting itch, and necessary for pain-induced itch suppression. Moreover, through brain-wide anterograde and retrograde viral tracing studies, we found that the RVMTacr1 neurons are bidirectionally connected with LPBN, periaqueductal gray (PAG), and lateral hypothalamic area (LHA). Thus, together, our data indicate that the RVMTacr1 neurons integrate nociceptive information to mediate itch-induced scratching and can mediate the physiological effects of itch through their downstream targets.

neuroscience↗

bioRxiv2023

A deep-learning driven investigation of circuit basis for reflexive hypersensitivity to pain

Objectively measuring animal behavior is key to understanding the neural circuits underlying pain. Recent progress in machine vision has presented us with unprecedented scope in behavioral analysis. Here, we apply DeeplabCut (DLC) to dissect mouse behavior on the thermal-plate test -- a commonly used paradigm to ascertain supraspinal contributions to noxious thermal sensation and pain hypersensitivity. We determine the signature characteristics of the pattern of mouse movement and posture in 3D in response to a range of temperatures from innocuous to noxious on the thermal-plate test. Next, we test how acute chemical and chronic inflammatory injuries sensitize mouse behaviors. Repeated exposure to noxious temperatures on the thermal-plate can induce learning, and in this study, we design a novel assay and formulate an analytical pipeline that will facilitate the dissection of plasticity mechanisms in pain circuits in the brain. Last, we record and test how activating Tacr1 expressing PBN neurons -- a population responsive to sustained noxious stimuli-affects mouse behavior on the thermal plate test. Taken together, we demonstrate that by tracking a single body part of a mouse, we can reveal the behavioral signatures of mice exposed to noxious surface temperatures, report the alterations of the same when injured, and determine if a molecularly and anatomically defined pain responsive circuit plays a role in the reflexive hypersensitivity to thermal pain.

neuroscience↗