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Reminders of mortality decrease midcingulate activity in response to others' suffering.

ABSTRACT: Reminders of mortality influence human social cognition, but whether and how reminders of mortality affect brain activity underlying social cognition remains unclear. To test whether increasing mortality salience modulates neural responses to others' suffering, we scanned healthy adults who viewed video clips showing others in pain using functional magnetic resonance imaging. One group of participants were primed to increase mortality salience and another group were primed with negative affect in terms of fear/anxiety. We found that perceiving painful vs non-painful stimuli in the pre-priming session activated the midcingulate/dorsal medial prefrontal cortex (MCC/dMPFC), bilateral anterior insula/inferior frontal cortex, bilateral secondary somatosensory cortex and left middle temporal gyrus. However, MCC/dMPFC activity in response to perceived pain in others was significantly decreased in the post-priming session by the mortality salience priming, but was not influenced by the negative affect priming. Moreover, subjective fear of death induced by the priming procedures mediated the change in MCC/dMPFC activity across the priming procedures. Subjective fear of death also moderated the co-variation of MCC/dMPFC and left insular activity during perception of others in pain. Our findings indicate that reminders of mortality decrease neural responses to others' suffering and this effect is mediated by the subjective fear of death.

SUBMITTER: Luo S

PROVIDER: S-EPMC3989130 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Reminders of mortality decrease midcingulate activity in response to others' suffering.

Luo Siyang S Shi Zhenhao Z Yang Xuedong X Wang Xiaoying X Han Shihui S

Social cognitive and affective neuroscience 20130117 4

Reminders of mortality influence human social cognition, but whether and how reminders of mortality affect brain activity underlying social cognition remains unclear. To test whether increasing mortality salience modulates neural responses to others' suffering, we scanned healthy adults who viewed video clips showing others in pain using functional magnetic resonance imaging. One group of participants were primed to increase mortality salience and another group were primed with negative affect i ...[more]

PMID: 23327932

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Project description:Metformin is a well-known antidiabetic medication, which, besides diabetes, may be involved into modulation of other age-related pathologies, including cancer. The study concerns 12 gene polymorphisms divided into 2 groups consisting of 6 genes each. The first group was composed from so-called "standard" (S) polymorphisms, for which the connection with metabolic response to metformin is already established. The second group included polymorphisms of genes encoding proteins possibly connected with diabetes mellitus type 2 (DM2), impaired glucose tolerance or cancer and entitled here as "associated" (A). A total of 156 postmenopausal women (average age 60.7 ± 0.7) were included, 37 of them healthy, 64 with type DM2 and concurrent treatment-naïve cancer (mostly breast, endometrial or colorectal cancer), 32 with DM2 without cancer, and 23 with treatment-naïve cancer and normal glucose tolerance. The leading metformin response S-marker in combined group of DM2 patients was the CC variant of OCT1-R61C polymorphism of organic cation transporter protein 1 gene. In cancer patients without DM2, this position belonged to AC and AA genotypes of OCT1_rs622342 polymorphism. Among the A-polymorphisms, GA variant of sex hormone-binding globulin gene SHBG_D356N was less frequently observed in DM2 patients with or without cancer. Besides, in diabetics, the same polymorphic variant of SHBG as well as GC genotype of oxidized lipoprotein receptor OLR1_G501C and GG genotype of locus rs11065987 near BRAP gene were carried rather often in combination with "metformin-positive" variant of OCT1_R61C. In addition, carriers of OCT1_R61C and OCT1_rs622342 polymorphisms with potentially positive reaction to metformin had higher insulin resistance score (HOMA-IR) values. Received data lead to the conclusion that postmenopausal diabetics, both with and without cancer, differ in genetic stigmata of potential response to metformin less than they differ from cancer patients without DM2. As genetic polymorphisms associated with metabolic and anticancer metformin (and, possibly, phenformin) effects may be different, this subject requires further investigation.

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Reminders of mortality decrease midcingulate activity in response to others' suffering.

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Reminders of mortality decrease midcingulate activity in response to others' suffering.

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