Summary
An 8‐week feeding trial was carried out using young hybrid sturgeon (♀Huso huso × ♂Acipenser schrenckii) to study the effects of dietary phosphorus (P) on growth performance, body composition, liver and serum antioxidant status as well as the effluent P content in the wintertime. Four puffed pellet diets were formulated to contain graded total P levels at 0.63, 1.15, 1.85, and 2.12%, respectively. Triplicate groups of hybrid sturgeon (494.21 ± 18.63 g) were reared in concrete ponds (2.0 × 1.2 × 1.4 m), and fed one of the four diets for 8 weeks. Weight gain and feeding rate significantly decreased with increasing dietary P content, and fish fed the 2.12% P diet had negative growth. With the increase in dietary P, whole body ash and P content significantly increased. There was no inverse relationship between the whole body lipid content and dietary P level in young hybrid sturgeon. Hybrid sturgeon liver exhibited higher superoxide dismutase, catalase and glutathione peroxidase activities in the 0.63 and 1.15% dietary P treatment groups than those in the other two groups. Serum alkaline phosphatase activity increased significantly with increasing dietary P. Discharge of P into the pond increased significantly with increasing dietary P. In conclusion, a dietary P content between 0.63 and 1.15% helped young hybrid sturgeon to activate their antioxidant defense system and eradicate the free radicals, in order to reduce the antioxidant damage, while still keeping total P content in the pond at a relatively low level during the winter months.
Purpose of the review
The abuse of opioids induces many terrible problems in human health and social stability. For opioid-dependent individuals, withdrawal memory can be reactivated by context, which is then associated with extremely unpleasant physical and emotional feelings during opioid withdrawal. The reactivation of withdrawal memory is considered one of the most important reasons for opioid relapse, and it also allows for memory modulation based on the reconsolidation phenomenon. However, studies exploring withdrawal memory modulation during the reconsolidation window are lacking. By summarizing the previous findings about the reactivation of negative emotional memories, we are going to suggest potential neural regions and systems for modulating opioid withdrawal memory.
Recent findings
Here, we first present the role of memory reactivation in its modification, discuss how the hippocampus participates in memory reactivation, and discuss the importance of noradrenergic signaling in the hippocampus for memory reactivation. Then, we review the engagement of other limbic regions receiving noradrenergic signaling in memory reactivation. We suggest that noradrenergic signaling targeting hippocampus neurons might play a potential role in strengthening the disruptive effect of withdrawal memory extinction by facilitating the degree of memory reactivation.
Summary
This review will contribute to a better understanding of the mechanisms underlying reactivation-dependent memory malleability and will provide new therapeutic avenues for treating opioid use disorders.
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