Biologia floral e sistema de reprodução de Jacquemontia multiflora (Choisy) Hallier f. (Convolvulaceae)

Aspectos da fenologia, biologia da polinização e reprodução de Jacquemontia multiflora foram estudados na Fazenda Catalunha, Santa Maria da Boa Vista-PE. J. multiflora é uma liana anual, que apresenta floração do tipo cornucópia, com pico desta fenofase no bimestre março/abril, que corresponde ao final da estação chuvosa. As flores estão reunidas em cimeiras que apresentam eixo principal desenvolvido, expondo as flores acima da folhagem. As flores são raso-campanuladas, azuis, inodoras e secretam pequenas quantidades de néctar. A antese é diurna, ocorrendo por volta da 5:30h., e a duração das flores é de aproximadamente nove horas, podendo ser consideradas como efêmeras. Abelhas Apidae e Halictidae são os visitantes mais frequentes. Apis mellifera e Trigona spinipes são consideradas como principais polinizadores desta espécie. Quanto ao sistema de reprodução J. multiflora é autógama facultativa, produzindo frutos e sementes por autopolinização manual (30%) e também por polinização cruzada (60%).

The effect of a low dose of clenbuterol on rat soleus muscle submitted to joint immobilization

The aim of the present study was to evaluate the effect of joint immobilization on morphometric parameters and glycogen content of soleus muscle treated with clenbuterol. Male Wistar (3-4 months old) rats were divided into 4 groups (N = 6 for each group): control, clenbuterol, immobilized, and immobilized treated with clenbuterol. Immobilization was performed with acrylic resin orthoses and 10 µg/kg body weight clenbuterol was administered subcutaneously for 7 days. The following parameters were measured the next day on soleus muscle: weight, glycogen content, cross-sectional area, and connective tissue content. The clenbuterol group showed an increase in glycogen (81.6%, 0.38 ± 0.09 vs 0.69 ± 0.06 mg/100 g; P < 0.05) without alteration in weight, cross-sectional area or connective tissue compared with the control group. The immobilized group showed a reduction in muscle weight (34.2%, 123.5 ± 5.3 vs 81.3 ± 4.6 mg; P < 0.05), glycogen content (31.6%, 0.38 ± 0.09 vs 0.26 ± 0.05 mg/100 mg; P < 0.05) and cross-sectional area (44.1%, 2574.9 ± 560.2 vs 1438.1 ± 352.2 µm²; P < 0.05) and an increase in connective tissue (216.5%, 8.82 ± 3.55 vs 27.92 ± 5.36%; P < 0.05). However, the immobilized + clenbuterol group showed an increase in weight (15.9%; 81.3 ± 4.6 vs 94.2 ± 4.3 mg; P < 0.05), glycogen content (92.3%, 0.26 ± 0.05 vs 0.50 ± 0.17 mg/100 mg; P < 0.05), and cross-sectional area (19.9%, 1438.1 ± 352.2 vs 1724.8 ± 365.5 µm²; P < 0.05) and a reduction in connective tissue (52.2%, 27.92 ± 5.36 vs 13.34 ± 6.86%; P < 0.05). Statistical analysis was performed using Kolmogorov-Smirnov and homoscedasticity tests. For the muscle weight and muscle glycogen content, two-way ANOVA and the Tukey test were used. For the cross-sectional area and connective tissue content, Kruskal-Wallis and Tukey tests were used. This study emphasizes the importance of anabolic pharmacological protection during immobilization to minimize skeletal muscle alterations resulting from disuse.