Simvastatin-induced cardiac autonomic control improvement in fructose-fed female rats

OBJECTIVE: Because autonomic dysfunction has been found to lead to cardiometabolic disorders and because studies have reported that simvastatin treatment has neuroprotective effects, the objective of the present study was to investigate the effects of simvastatin treatment on cardiovascular and autonomic changes in fructose-fed female rats. METHODS: Female Wistar rats were divided into three groups: controls (n=8), fructose (n=8), and fructose+ simvastatin (n=8). Fructose overload was induced by supplementing the drinking water with fructose (100 mg/L, 18 wks). Simvastatin treatment (5 mg/kg/day for 2 wks) was performed by gavage. The arterial pressure was recorded using a data acquisition system. Autonomic control was evaluated by pharmacological blockade. RESULTS: Fructose overload induced an increase in the fasting blood glucose and triglyceride levels and insulin resistance. The constant rate of glucose disappearance during the insulin intolerance test was reduced in the fructose group (3.4+ 0.32%/min) relative to that in the control group (4.4+ 0.29%/min). Fructose+simvastatin rats exhibited increased insulin sensitivity (5.4+0.66%/min). The fructose and fructose+simvastatin groups demonstrated an increase in the mean arterial pressure compared with controls rats (fructose: 124+2 mmHg and fructose+simvastatin: 126 + 3 mmHg vs. controls: 112 + 2 mmHg). The sympathetic effect was enhanced in the fructose group (73 + 7 bpm) compared with that in the control (48 + 7 bpm) and fructose+simvastatin groups (31+8 bpm). The vagal effect was increased in fructose+simvastatin animals (84 + 7 bpm) compared with that in control (49 + 9 bpm) and fructose animals (46+5 bpm). CONCLUSION: Simvastatin treatment improved insulin sensitivity and cardiac autonomic control in an experimental model of metabolic syndrome in female rats. These effects were independent of the improvements in the classical plasma lipid profile and of reductions in arterial pressure. These results support the hypothesis that statins reduce the cardiometabolic risk in females with metabolic syndrome

Hypertension induces additional cardiometabolic impairments and attenuates aerobic exercise training adaptations in fructose-fed ovariectomized rats

We tested whether hypertension favors the development of additional cardiometabolic changes in fructose-fed ovariectomized rats and how it affects aerobic exercise training (ET) effects. All rats received fructose in drinking water (10%) beginning at weaning, were ovariectomized at 10 weeks of age and divided into the normotensive sedentary (NFOS) and trained (NFOT) and hypertensive sedentary (HFOS) and trained (HFOT) groups. ET was performed on a treadmill. Arterial pressure (AP) was directly recorded; heart rate and AP variabilities were analyzed. Lipoperoxidation (LPO) and antioxidant enzyme levels were measured in the left ventricle. In addition to increased AP levels, when compared with the NFOS group, the hypertensive groups had resting tachycardia, a reduction of 29% in the pulse interval variance (VAR-PI), 19% in RMSSD (root mean square of successive differences, a cardiac parasympathetic index) and 53% in the α-index (spontaneous baroreflex), while the systolic AP variance (VAR-SAP) and its low-frequency band (LF-SAP) were sharply increased. ET did not alter AP levels. Even in the presence of hypertension, ET induced resting bradycardia, decreases of 33% in VAR-SAP and 49% in LF-SAP, and an increase of more than 60% in VAR-PI and the α-index. However, some of these parameters were still impaired relative to those of normotensive rats. LPO was reduced and catalase was increased in both trained groups, with no difference between the normotensive and hypertensive groups. Negative correlations were obtained between LPO and RMSSD (r=-0.60, P<0.05) and α-index (r=-0.63, P<0.05). In conclusion, hypertension augmented the dysfunctions in fructose-fed ovariectomized rats and attenuated metabolic aerobic ET benefits. These changes may be related to cardiovascular autonomic and oxidative stress alterations.Fil: De Brito Monzani, Janaina O.. Universidade Federal do Maranhao; BrasilFil: Sanches, Iris Callado. Universidade São Judas Tadeu ; BrasilFil: Bernardes, Nathalia. Universidade Nove de Julho; BrasilFil: Ponciano, Kátia. Universidade São Judas Tadeu ; BrasilFil: Moraes Silva, Ivana C.. Universidade de Sao Paulo; BrasilFil: Irigoyen, Maria Cláudia. Universidade de Sao Paulo; BrasilFil: Llesuy, Susana Francisca. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Química Analítica y Fisicoquímica. Cátedra de Química General e Inorgánica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Bioquímica y Medicina Molecular. Universidad de Buenos Aires. Facultad Medicina. Instituto de Bioquímica y Medicina Molecular; ArgentinaFil: De Angelis, Kátia. Universidade Nove de Julho; Brasi

Small forest losses degrade stream macroinvertebrate assemblages in the eastern Brazilian Amazon

Generally, habitat loss and fragmentation negatively affect biota, often in nonlinear ways. Such nonlinear responses suggest the existence of critical limits for habitat loss beyond which taxa experience substantial changes. Therefore, we identified change points for aquatic macroinvertebrate assemblages at both local-riparian and catchment extents in response to a forest-loss gradient in agriculture-altered landscapes of 51 small (1st to 3rd Strahler order) eastern Amazon streams. We used Threshold Indicator Taxa Analysis (TITAN) to identify change points for individual taxa and segmented regression analysis for assemblage richness. Considering the patterns of the cumulative frequency distributions of sum(Z−) maxima across bootstrap replications, peak changes in macroinvertebrate assemblages were at ∼9% (5–95 percentiles = 1–15%) of forest-loss at the catchment extent, and at ∼1.4% (5–95 percentiles = 0–35%) of forest-loss at the local-riparian extent. Although the assemblage change point at the site extent was less than that detected at the catchment extent, the markedly lower percentile range indicates that biotic assemblages are more clearly responsive to forest-loss at the catchment/network-riparian extents than the site extent. For catchment and site extents, segmented regression analysis determined a change point for assemblage richness at 57% and 79% of forest-loss, respectively. This indicates the low capacity of total richness to separate early and synchronous decreases of sensitive taxa from gradual increases of tolerant taxa. Our results also show that it is not enough to focus management and conservation actions on riparian zones, but that conservation strategies should be expanded to entire catchments as well. The sharp decline of sensitive taxa in response to removal of a small portion of forest cover, even at catchment extents, indicates that the Brazilian Forest Code is insufficient for protecting stream macroinvertebrates. Consequently, we recommend strategies to reverse the potential collapse of aquatic biodiversity, particularly through avoiding deforestation and forest degradation, encouraging socio-economic incentives for restoring degraded areas, creating protected areas, and maintaining the current protected areas. We argue that reducing habitat loss should be a top priority for conservation planners in tropical forests because the sensitivity of aquatic biodiversity to removal of riparian forest-cover in Amazon rainforests is higher than previously thought. Therefore, the Forest Code regulatory framework needs complementary regulation that may be achived by more restrictive State and biome policies. © 2019 Elsevier Lt

Pervasive gaps in Amazonian ecological research

Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear un derstanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5–7 vast areas of the tropics remain understudied.8–11 In the American tropics, Amazonia stands out as the world’s most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepre sented in biodiversity databases.13–15 To worsen this situation, human-induced modifications16,17 may elim inate pieces of the Amazon’s biodiversity puzzle before we can use them to understand how ecological com munities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple or ganism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region’s vulnerability to environmental change. 15%–18% of the most ne glected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lostinfo:eu-repo/semantics/publishedVersio

A social and ecological assessment of tropical land uses at multiple scales: the Sustainable Amazon Network

Science has a critical role to play in guiding more sustainable development trajectories. Here, we present the Sustainable Amazon Network (Rede Amazonia Sustentavel, RAS): a multidisciplinary research initiative involving more than 30 partner organizations working to assess both social and ecological dimensions of land-use sustainability in eastern Brazilian Amazonia. The research approach adopted by RAS offers three advantages for addressing land-use sustainability problems: (i) the collection of synchronized and co-located ecological and socioeconomic data across broad gradients of past and present human use; (ii) a nested sampling design to aid comparison of ecological and socioeconomic conditions associated with different land uses across local, landscape and regional scales; and (iii) a strong engagement with a wide variety of actors and non-research institutions. Here, we elaborate on these key features, and identify the ways in which RAS can help in highlighting those problems in most urgent need of attention, and in guiding improvements in land-use sustainability in Amazonia and elsewhere in the tropics. We also discuss some of the practical lessons, limitations and realities faced during the development of the RAS initiative so far.Keywords: Social–ecological systems, Tropical forests, Land use, Interdisciplinary research, Sustainability, Trade-off

Pervasive gaps in Amazonian ecological research

Biodiversity loss is one of the main challenges of our time,1,2 and attempts to address it require a clear understanding of how ecological communities respond to environmental change across time and space.3,4 While the increasing availability of global databases on ecological communities has advanced our knowledge of biodiversity sensitivity to environmental changes,5,6,7 vast areas of the tropics remain understudied.8,9,10,11 In the American tropics, Amazonia stands out as the world's most diverse rainforest and the primary source of Neotropical biodiversity,12 but it remains among the least known forests in America and is often underrepresented in biodiversity databases.13,14,15 To worsen this situation, human-induced modifications16,17 may eliminate pieces of the Amazon's biodiversity puzzle before we can use them to understand how ecological communities are responding. To increase generalization and applicability of biodiversity knowledge,18,19 it is thus crucial to reduce biases in ecological research, particularly in regions projected to face the most pronounced environmental changes. We integrate ecological community metadata of 7,694 sampling sites for multiple organism groups in a machine learning model framework to map the research probability across the Brazilian Amazonia, while identifying the region's vulnerability to environmental change. 15%–18% of the most neglected areas in ecological research are expected to experience severe climate or land use changes by 2050. This means that unless we take immediate action, we will not be able to establish their current status, much less monitor how it is changing and what is being lost

Low forest-loss thresholds threaten Amazonian fish and macroinvertebrate assemblage integrity

Deforestation is a major threat globally, but especially in tropical regions because they are biodiversity strongholds and carbon storehouses. Some studies have reported changes in species richness and composition in lotic ecosystems with increased forest-loss in their catchment, presumably resulting from the replacement of sensitive taxa by more resistant or tolerant taxa. Also, sensitive taxa respond to deforestation in a non-linear manner and fish and macroinvertebrates have different sensitivities to landscape pressures. Therefore, it is useful to determine the effects of forest-loss on widespread sensitive or threshold taxa in aquatic ecosystems. We used Threshold Indicator Taxa Analysis (TITAN) to assess forest-loss and land use history impacts in 92 eastern Amazonian stream sites. We determined TITAN peak-change thresholds for fish at 1% and 6% of forest-loss at total-catchment and local-riparian spatial extents, respectively, and at 2% and 40% of land-use intensity change at total-catchment and local-riparian spatial extents, respectively. For macroinvertebrates, TITAN peak-change thresholds were 1% and 11% of forest loss at total-catchment and local-riparian spatial extents, respectively, and at 3% of land-use intensity change for both total-catchment and local-riparian spatial extents. Because of these thresholds, inherent ecoregional variability and key literature, we have three major recommendations. 1) Logging should be prohibited in riparian reserves that are at least 100-m wide on each side of headwater streams and in a network of catchments across all biomes and as many landscape types as possible. 2) An ecologically and statistically rigorous monitoring program with standard methods should be implemented to assess and regulate land uses better. 3) Conservation planning areas should consider aquatic biota as well as terrestrial biota