Carmichael S W, Stoddard S L, O'Connor D T, Yaksh T L, Tyce G M
Department of Anatomy, Mayo Clinic/Foundation, Rochester, MN 55905.
Neuroscience. 1990;34(2):433-40. doi: 10.1016/0306-4522(90)90152-t.
Secretion of the adrenal medulla was stimulated in nine cats by insulin-induced hypoglycemia. Levels of catecholamines (mol. wt 153-183), neuropeptide Y (mol. wt 4254) and chromogranin A (mol. wt 48,000) were measured in concurrently collected samples of adrenolumbar venous blood and thoracic duct lymph for up to 4 h following insulin administration. Insulin-induced hypoglycemia elicited an increase in the secretion of catecholamines, which reached peak levels in the adrenolumbar venous plasma at 1.5-2 h and in the lymph at 2.5 h. Although catecholamines were the most numerous measured molecules in the lymph, levels of norepinephrine and epinephrine were 75-250-fold less than those found in the adrenolumbar venous plasma. Neuropeptide Y in the adrenolumbar venous plasma reached peak levels between 1 and 1.5 h; at this time approximately 20% of the peak venous amount was detected in the lymph. Chromogranin A was found in approximately equal amounts in both plasma and lymph; the peak level in the plasma occurred at 1.5-2 h, while that in the lymph was reached at 2-3 h. We suggest that the size of a molecule influences the route it takes following exocytosis from the chromaffin vesicle. Smaller molecules such as catecholamines may pass directly into the circulation, while larger molecules such as chromogranin A may be temporarily sequestered in the interstitial space before passing into the lymph, and hence into the circulation.
通过胰岛素诱导的低血糖刺激了9只猫的肾上腺髓质分泌。在注射胰岛素后的长达4小时内,对同时采集的肾上腺腰静脉血和胸导管淋巴样本中的儿茶酚胺(分子量153 - 183)、神经肽Y(分子量4254)和嗜铬粒蛋白A(分子量48,000)水平进行了测量。胰岛素诱导的低血糖引起儿茶酚胺分泌增加,其在肾上腺腰静脉血浆中于1.5 - 2小时达到峰值水平,在淋巴中于2.5小时达到峰值水平。尽管儿茶酚胺是淋巴中检测到的数量最多的分子,但去甲肾上腺素和肾上腺素的水平比肾上腺腰静脉血浆中的水平低75 - 250倍。肾上腺腰静脉血浆中的神经肽Y在1至1.5小时之间达到峰值水平;此时在淋巴中检测到约为静脉峰值量的20%。嗜铬粒蛋白A在血浆和淋巴中的含量大致相等;血浆中的峰值水平出现在1.5 - 2小时,而淋巴中的峰值水平在2 - 3小时达到。我们认为分子大小会影响其从嗜铬小泡胞吐后所采取的途径。较小的分子如儿茶酚胺可能直接进入循环,而较大的分子如嗜铬粒蛋白A可能在进入淋巴进而进入循环之前暂时滞留在间质空间中。