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<P>Nitrogen (N) availability is a key regulator of carbon (C) cycling in terrestrial ecosystems. Anthropogenic N input, such as N deposition and fertilization, increases N availability in soil, which has important implications for an ecosystem’s C storage and loss. Soil respiration (Rs), which is the second largest C flux from terrestrial ecosystems to the atmosphere, plays an important role in terrestrial C cycles. The direction and magnitude of the responses of Rs and its components to N addition have been widely evaluated, but it remains unclear how these processes change across multiple N addition levels. Here we conducted a two-year field experiment to examine the changes of Rs and its autotrophic respiration (Ra) and heterotrophic respiration (Rh) components along a gradient of eight N levels (0, 1 2, 4, 8, 16, 24, 32 g m<SUP>−2</SUP> yr<SUP>−1</SUP>) in a Tibetan alpine steppe, and used structural equation modeling (SEM) to explore the relative contributions of biotic and abiotic variables and their direct and indirect pathways regulating the Ra and Rh. Our results indicated that both Rs and Ra exhibited first increasing and then subsequent decreasing trends at the threshold of 8 g N m<SUP>−2</SUP> yr<SUP>−1</SUP>. In contrast, the Rh declined linearly with the N addition rate continuously increasing. SEM analysis revealed that, among various environmental factors, soil temperature was the most important one modulating Rs, which not only had a direct effect on the two Rs components, but also indirectly regulated the Ra and Rh via root and microbial biomass. These findings suggest that the nonlinear response patterns of Rs should be considered for better predicting terrestrial C balance, given that anthropogenic N input to the terrestrial ecosystems is increasing continuously.</P>
Chronic inflammation is associated with various chronic illnesses including immunity disorders, cancer, neurodegeneration, and vascular diseases. Iridoids are compounds with anti-inflammatory properties. However their anti-inflammatory mechanism remains unclear. Here, we report that scropolioside B, isolated from a Tibetan medicine (Scrophularia dentata Royle ex Benth.), blocked expressions of TNF, IL-1, and IL-32 through NF-κB pathway. Scropolioside B inhibited NF-κB activity in a dose-dependent manner with IC50 values of 1.02 μmol/L. However, catalpol, similar to scropolioside B, was not effective in inhibiting NF-κB activity. Interestingly, scropolioside B and catalpol decreased the expression of NLRP3 and cardiolipin synthetase at both the mRNA and protein level. Our results showed that scropolioside B is superior in inhibiting the expression, maturation, and secretion of IL-1β compared to catalpol. These observations provide further understanding of the anti-inflammatory effects of iridoids and highlight scropolioside B as a potential drug for the treatment of rheumatoid arthritis and atherosclerosis.