Table 2.

Depolarization-induced changes in immunolabeling intensity

SpeciesTissue/labelControlHigh K+Change (%)P value
Cancer borealis AMC/SIFa 169.8±5.5 164.5±6.6 -3.1±1.9 0.0088 
 PMC/TRP 158.8±8.5 150.2±7.1 -5.4±1.7 0.0009 
Cancer productus AMC/SIFa 171.8±6.3 165.0±6.0 -4.0±0.6 <0.0001 
 PMC/TRP 168.7±4.6 160.2±5.0 -5.0±2.3 0.0032 
Cancer magister AMC/SIFa 164.7±9.3 158.3±7.6 -3.8±2.2 0.0083 
 PMC/TRP 161.7±8.6 155.0±9.1 -4.1±0.9 <0.0001 
SpeciesTissue/labelControlHigh K+Change (%)P value
Cancer borealis AMC/SIFa 169.8±5.5 164.5±6.6 -3.1±1.9 0.0088 
 PMC/TRP 158.8±8.5 150.2±7.1 -5.4±1.7 0.0009 
Cancer productus AMC/SIFa 171.8±6.3 165.0±6.0 -4.0±0.6 <0.0001 
 PMC/TRP 168.7±4.6 160.2±5.0 -5.0±2.3 0.0032 
Cancer magister AMC/SIFa 164.7±9.3 158.3±7.6 -3.8±2.2 0.0083 
 PMC/TRP 161.7±8.6 155.0±9.1 -4.1±0.9 <0.0001 

Paired anterior midgut caeca (AMCs) and the single posterior midgut caecum(PMC) from six individual crabs were isolated, and each PMC was divided into two pieces. After 1 h of incubation in control saline, the saline surrounding one member of each tissue pair was replaced with control saline, whereas the other was replaced with high-K+ saline. After 1 h, all tissues were simultaneously immunoprocessed for either SIFamide (SIFa)- or substance P(TRP)-like labeling. Values shown are the mean pixel values for each of the six preparations. Paired two-tailed Student's t-tests were used to compare labeling intensity in control and high-K+ saline(P value). No statistically significant differences were seen in C. borealis tissue pairs when both AMCs or PMC sections were incubated in the same saline (N=6 pairs per tissue and saline; data not shown).

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