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Long‐chain polyunsaturated fatty acids (LC‐PUFAs) play crucial roles in growth, development and reproduction of Litopenaeus vannamei, one of the most important shrimp species cultivated in China in recent years. To investigate the effect of dietary n‐3 PUFA composition on growth and the expression of LvFAD6 and LvELOV5 genes and fatty acid composition of this species, ten diets, which contain different levels of α‐linolenic acid (C18:3 n‐3, ALA), eicosapentaenoic acid (C20:5 n‐3, EPA) and docosahexaenoic acid (C22:6 n‐3, DHA), respectively, were prepared for the culture of this species lasting 42 days. The results showed that the identified cDNA sequence of fatty acyl desaturases 6 from L. vannamei (LvFAD6) was 739 bp, encoding a protein of 210 amino acids. The LvFAD6 peptide sequence possessed two histidine‐rich motifs (QHHA and QIEHH), shared 96.6% identity with Apostichopus japonicus FAD6 and strongly clustered with FAD6 from A. japonicus and Octopus bimaculoides. The expression of LvFAD6 and LvELOV5 in muscle decreased with increase in dietary EPA, but increased with increase in dietary DHA. Dietary ALA has the potential to further increase the production of these health‐beneficial LC‐PUFAs in L. vannamei fed a diet with low levels of EPA and DHA, implying L. vannamei had the capacity to convert dietary ALA into EPA and DHA. These results suggest that the supplementation of ALA, EPA and DHA in diets for better growth of L. vannamei in ranges of 2.5% to 3.89%, 1.7% to 3.19% and 2.7% to 5.84% of total fatty acids respectively. [ABSTRACT FROM AUTHOR]

Background and Purpose. The vascular morphology in crowd with family history of stroke remains unclear. The present study clarified the characteristics of the intracranial vascular CoW and prevalence of intracranial aneurysms in subjects with family history of stroke. Methods. A stratified cluster, random sampling method was used for subjects with family history of stroke among rural residents in Jixian, Tianjin, China. All the subjects underwent a physical examination, head computed tomography (CT) scan, and cephalic and cervical computed tomography angiography (CTA) scan. Anatomic variations in the Circle of Willis and cerebrovascular disease in this population were analyzed. Results. In the crowd with similar living environment, stable genetic background, and family history of stroke and without obvious nerve function impairment (1) hypoplasia or absence of A1 segment was significantly different in gender (male versus female: 9.8% versus 18.8%, p=0.031), especially the right-side A1 (male versus female: 5.9% versus 16.4%, p=0.004). (2) Hypoplasia or absence of bilateral posterior communicating arteries was more common in men than women (58.2% versus 45.3%, p=0.032). Unilateral fetal posterior cerebral artery was observed more often in women than men (17.2% versus 8.5%, p=0.028). (3) The percentage of subjects with incomplete CoW did not increase significantly with age. Compared to healthy Chinese people, the crowd had a higher percentage of incomplete CoW (p<0.001). (4) No obvious correlation between risk factors and CoW was found. (5) The prevalence of aneurysm was 10.3% in the special crowd. Conclusions. The certain variations of CoW showed significant relation to gender, but not to age in people with family history of stroke. The incomplete circle may be a dangerous factor that is independent of common risk factors for stroke and tend to lead to cerebral ischemia in the crowd with family history of stroke. The prevalence of intracranial aneurysm is comparatively high in the present subjects compared to other people. [ABSTRACT FROM AUTHOR]