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Patients with chronic pain, especially orofacial pain, often suffer from affective disorders, including anxiety. Previous studies largely focused on the role of the caudal anterior cingulate cortex (cACC) in affective responses to pain, long-term potentiation (LTP) in cACC being thought to mediate the interaction between anxiety and chronic pain. But recent evidence indicates that the rostral ACC (rACC), too, is implicated in processing affective pain. However, whether such processing is associated with neuronal and/or synaptic plasticity is still unknown. We addressed this issue in a chronic facial inflammatory pain model (complete Freund's adjuvant model) in rats, by combining behavior, Fos protein immunochemistry and ex vivo intracellular recordings in rACC slices prepared from these animals. Facial mechanical allodynia occurs immediately after CFA injection, peaks at post-injection day 3 and progressively recovers until post-injection days 10–11, whereas anxiety is delayed, being present at post-injection day 10, when sensory hypersensitivity is relieved, but, notably, not at post-injection day 3. Fos expression reveals that neuronal activity follows a bi-phasic time course in bilateral rACC: first enhanced at post-injection day 3, it gets strongly depressed at post-injection day 10. Ex vivo recordings from lamina V pyramidal neurons, the rACC projecting neurons, show that both their intrinsic excitability and excitatory synaptic inputs have undergone long-term depression (LTD) at post-injection day 10. Thus chronic pain processing is associated with dynamic changes in rACC activity: first enhanced and subsequently decreased, at the time of anxiety-like behavior. Chronic pain-induced anxiety might thus result from a rACC deactivation-cACC hyperactivation interplay. • Facial inflammation leads to immediate mechanical allodynia and delayed anxiety. • Elevated rostral ACC neuronal activity is associated with pain hypersensitivity. • Notably depressed rostral ACC neuronal activity is associated with delayed anxiety. • Rostral ACC layer V projecting neurons are deactivated over the period of anxiety. • Rostral ACC deactivation-caudal ACC hyperactivation interplay may initiate anxiety. [ABSTRACT FROM AUTHOR]

Abstract: Exposure of anestrous females to a ram or his odour induces rapid secretion of LH that can lead to ovulation. This response is mediated by the main olfactory system (MOS) in sexually experienced ewes. The accessory olfactory system (AOS) has a minor, but unclear, role in this response. In sexually naive ewes, male odour is less effective than in experienced ewes, but the neural pathway involved is not known. In our experiment, we investigated the brain regions activated by the male or his odour in young and sexually naive anestrous ewes using immunohistochemistry for Fos alone, Fos double-labeled with Gonadotropin-Releasing Hormone (GnRH) or with Tyrosine Hydroxylase (TH). Ram odour caused neural activation in the main olfactory bulb (MOB) and not the AOS. Exposure to a male induced significant activation in the MOB, the cortical and medial nuclei of the amygdala and the ventromedial hypothalamus but not in cortical areas, or in GnRH or TH positive neurons. These results confirm the predominant role of the MOS in the detection of olfactory signals in sheep and underline the importance of learning processes. [Copyright &y& Elsevier]